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<h1><a data-section="Header" data-ga-action="Click-on"
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data-ga-label="dbSNP Short Genetic Variations"
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ref="section=Header&action=Click-on&label=dbSNP Short Genetic Variations"
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href="/snp/">dbSNP</a>
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<span class="uswds-gray tagline">Short Genetic Variations</span>
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</h1>
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<div class="usa-alert-body">
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<h3 class="usa-alert-heading">Welcome to the Reference SNP (rs) Report</h3>
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<p class="usa-alert-text">All alleles are reported in the <a href="https://www.ncbi.nlm.nih.gov/core/assets/snp/docs/RefSNP_orientation_updates.pdf" target="_blank"
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data-ga-action="Click for forward orientation" data-ga-category="Info panel"
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data-ga-label="Forward orientation">Variant Details tab</a> for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the
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<div class="usa-width-one-half">
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<h3>Reference SNP (rs) Report</h3>
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</div>
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<div class="usa-width-one-half">
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<ul class="utilities usa-unstyled-list align-right">
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<li title="Download in API JSON format"><a href="https://api.ncbi.nlm.nih.gov/variation/v0/refsnp/1042522"
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class="fa fa-question-circle ncbiPopper" id="mainhelp_tooltip"
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ref="section=Main&action=Click-on-Tooltip&label=main_tp"><span class="usa-sr-only">Help</span></a>
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<p id="main_tp">
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This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.<br/>
|
||
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.<br/>
|
||
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors. <br/>
|
||
For more information see <a class="external-link" href="/snp/docs/refsnp_report/helpdoc"> Help documentation</a>.</p>
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<div class="usa-grid-full clearfix">
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<div class="usa-width-two-thirds">
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<div class="blue-box">
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<h2 id="refsnp_id">rs1042522</h2>
|
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</div>
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</div>
|
||
<div class="accession usa-width-one-third">
|
||
<p>Current Build <span>156</span></p>
|
||
<p>Released <span>
|
||
|
||
September 21, 2022
|
||
|
||
</span></p>
|
||
</div>
|
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</div>
|
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|
||
|
||
|
||
<div class="summary-box usa-grid-full">
|
||
<dl class="usa-width-one-half">
|
||
|
||
<dt>Organism</dt>
|
||
<dd class="species_name">Homo sapiens</dd>
|
||
|
||
|
||
|
||
|
||
<dt>Position</dt>
|
||
<dd>
|
||
|
||
<span>chr17:7676154 </span><span>(GRCh38.p14) </span><a data-width="640px" href="#pos_tp"
|
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ref="section=Summary&action=Click-on-Tooltip&label=pos_tp"
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data-section="Summary" data-ga-action="Click-on-Tooltip"
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data-ga-label="pos_tp" class="fa fa-question-circle ncbiPopper" id="position_tooltip"><span class="usa-sr-only">Help</span></a><p id="pos_tp">The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See <a href="/snp/docs/refsnp_report/helpdoc/">here</a> for details.</p>
|
||
|
||
|
||
</dd>
|
||
|
||
|
||
|
||
<dt>Alleles</dt>
|
||
<dd>
|
||
|
||
|
||
G>A / G>C / G>T
|
||
|
||
</dd>
|
||
|
||
|
||
|
||
|
||
<dt>Variation Type</dt>
|
||
<dd>
|
||
|
||
SNV
|
||
|
||
|
||
|
||
<span class="small-font gray">Single Nucleotide Variation</span>
|
||
|
||
</dd>
|
||
|
||
|
||
|
||
<dt>Frequency</dt>
|
||
<dd>
|
||
|
||
<div>
|
||
G=0.382621
|
||
(101276/264690, TOPMED)
|
||
</div><div>
|
||
G=0.331835
|
||
(83136/250534, GnomAD_exome)
|
||
</div><span>
|
||
G=0.373457 (52281/139992, GnomAD)
|
||
</span><span>(<a id="expandfrequency" data-freq-remn="23"
|
||
data-is-icon="false" data-section="Summary" data-ga-action="Click-on"
|
||
data-ga-label="Frequency" data-targets="#remn_summ_freq" href="#remn_summ_freq"
|
||
ref="section=Summary&action=Click-on&label=Frequency">+ 23 more</a>)</span><div class="ui-widget hide_elm" id="remn_summ_freq"><div>
|
||
G=0.340040
|
||
(41119/120924, ExAC)
|
||
</div><div>
|
||
G=0.285663
|
||
(30142/105516, ALFA)
|
||
</div><div>
|
||
G=0.34980
|
||
(9884/28256, 14KJPN)
|
||
</div><div>
|
||
G=0.35523
|
||
(5953/16758, 8.3KJPN)
|
||
</div><div>
|
||
G=0.4561
|
||
(2921/6404, 1000G_30x)
|
||
</div><div>
|
||
G=0.4571
|
||
(2289/5008, 1000G)
|
||
</div><div>
|
||
G=0.3004
|
||
(1346/4480, Estonian)
|
||
</div><div>
|
||
G=0.2504
|
||
(965/3854, ALSPAC)
|
||
</div><div>
|
||
G=0.2446
|
||
(907/3708, TWINSUK)
|
||
</div><div>
|
||
G=0.3446
|
||
(1009/2928, KOREAN)
|
||
</div><div>
|
||
G=0.3638
|
||
(665/1828, Korea1K)
|
||
</div><div>
|
||
G=0.419
|
||
(331/790, PRJEB37584)
|
||
</div><div>
|
||
G=0.404
|
||
(270/668, PharmGKB)
|
||
</div><div>
|
||
C=0.495
|
||
(304/614, Vietnamese)
|
||
</div><div>
|
||
G=0.330
|
||
(198/600, NorthernSweden)
|
||
</div><div>
|
||
G=0.283
|
||
(151/534, MGP)
|
||
</div><div>
|
||
G=0.267
|
||
(111/416, SGDP_PRJ)
|
||
</div><div>
|
||
G=0.439
|
||
(143/326, HapMap)
|
||
</div><div>
|
||
G=0.289
|
||
(88/304, FINRISK)
|
||
</div><div>
|
||
G=0.463
|
||
(100/216, Qatari)
|
||
</div><div>
|
||
G=0.11
|
||
(6/56, Ancient Sardinia)
|
||
</div><div>
|
||
G=0.18
|
||
(8/44, Siberian)
|
||
</div><div>
|
||
G=0.33
|
||
(13/40, GENOME_DK)
|
||
</div></div>
|
||
|
||
</dd>
|
||
|
||
</dl>
|
||
<dl class="usa-width-one-half">
|
||
|
||
<dt>Clinical Significance</dt>
|
||
<dd>
|
||
|
||
Reported in <a target="_blank" data-section="Summary" data-ga-action="Click-on"
|
||
data-ga-label="Reported in ClinVar"
|
||
ref="section=Summary&action=Click-on&label=Reported in ClinVar"
|
||
href="/clinvar?term=((176504[AlleleID])OR(185405[AlleleID])OR(27390[AlleleID])OR(846295[AlleleID]))">ClinVar</a>
|
||
|
||
</dd>
|
||
|
||
|
||
|
||
<dt>Gene : Consequence</dt>
|
||
<dd>
|
||
|
||
<span>TP53 : Missense Variant</span>
|
||
|
||
</dd>
|
||
|
||
<dt>Publications</dt>
|
||
<dd>
|
||
|
||
<a id="snp_pub_count" href="#publications">390
|
||
citations
|
||
</a>
|
||
|
||
</dd>
|
||
|
||
|
||
<dt>Genomic View</dt>
|
||
<dd>
|
||
<a href="#seq_hash" data-section="Summary" data-ga-action="Click-on"
|
||
data-ga-label="Genomic View See rs on genome"
|
||
ref="section=Summary&action=Click-on&label=Genomic View See rs on genome">See rs on
|
||
genome</a>
|
||
</dd>
|
||
|
||
</dl>
|
||
</div>
|
||
|
||
|
||
|
||
<div class="js-tabs">
|
||
<ul class="js-tablist" data-section="Tab">
|
||
|
||
<li class="js-tablist__item">
|
||
<a href="#frequency_tab" ref="section=Tab&action=Click-on&label=Frequency"
|
||
data-ga-action="Click-on-horizontal" data-ga-label="Frequency" id="label_id_third"
|
||
class="js-tablist__link">Frequency
|
||
<span aria-hidden="true"></span></a>
|
||
</li>
|
||
|
||
<li class="js-tablist__item">
|
||
<a href="#variant_details" ref="section=Tab&action=Click-on&label=Variant Details"
|
||
data-ga-action="Click-on-horizontal" data-ga-label="Variant Details" id="label_id_first"
|
||
class="js-tablist__link">Variant Details
|
||
<span class="js-tablist__item-has-focus" aria-hidden="true"></span></a>
|
||
</li>
|
||
<li class="js-tablist__item">
|
||
<a href="#clinical_significance"
|
||
ref="section=Tab&action=Click-on&label=Clinical Significance"
|
||
data-ga-action="Click-on-horizontal" data-ga-label="Clinical Significance" id="label_id_second"
|
||
class="js-tablist__link">Clinical
|
||
Significance
|
||
<span aria-hidden="true"></span></a>
|
||
</li>
|
||
<li class="js-tablist__item">
|
||
<a href="#hgvs_tab" ref="section=Tab&action=Click-on&label=HGVS"
|
||
data-ga-action="Click-on-horizontal" data-ga-label="HGVS" id="label_id_fourth"
|
||
class="js-tablist__link">HGVS
|
||
<span aria-hidden="true"></span></a>
|
||
</li>
|
||
<li class="js-tablist__item">
|
||
<a href="#submissions" ref="section=Tab&action=Click-on&label=Submissions"
|
||
data-ga-action="Click-on-horizontal" data-ga-label="Submissions" id="label_id_fifth"
|
||
class="js-tablist__link">Submissions
|
||
<span aria-hidden="true"></span></a>
|
||
</li>
|
||
<li class="js-tablist__item">
|
||
<a href="#history" ref="section=Tab&action=Click-on&label=History"
|
||
data-ga-action="Click-on-horizontal" data-ga-label="History" id="label_id_sixth"
|
||
class="js-tablist__link">History
|
||
<span aria-hidden="true"></span></a>
|
||
</li>
|
||
<li class="js-tablist__item">
|
||
<a href="#publications" ref="section=Tab&action=Click-on&label=Publications"
|
||
data-ga-action="Click-on-horizontal" data-ga-label="Publications" id="label_id_seventh"
|
||
class="js-tablist__link">Publications
|
||
<span aria-hidden="true"></span></a>
|
||
</li>
|
||
<li class="js-tablist__item">
|
||
<a href="#flanks" ref="section=Tab&action=Click-on&label=Flanks"
|
||
data-ga-action="Click-on-horizontal" data-ga-label="Flanks" id="label_id_eighth"
|
||
class="js-tablist__link">Flanks
|
||
<span aria-hidden="true"></span></a>
|
||
</li>
|
||
|
||
</ul>
|
||
<div id="frequency_tab" class="js-tabcontent">
|
||
|
||
|
||
|
||
|
||
|
||
<a data-width="640px" href="#popfreq_tp"
|
||
ref="section=Frequency&action=Click-on-Popper&label=popfreq_tp"
|
||
data-section="Frequency" data-ga-action="Click-on-Popper"
|
||
data-ga-label="popfreq_tp" >
|
||
</a>
|
||
<p id="popfreq_tp">
|
||
<font size="5" color="blue"><strong><a href="/snp/docs/gsr/alfa" rel="nofollow" target="_blank">ALFA Allele Frequency</a></strong></font><br/>
|
||
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project <a href="/snp/docs/gsr/alfa" rel="nofollow" target="_blank">page</a> including descriptions, data access, and terms of use.
|
||
|
||
</p>
|
||
|
||
<div>
|
||
<span class="build_id_container"><span class="build_id_label">Release Version:</span> 20231103111315</span>
|
||
</div>
|
||
|
||
<div id="popfreq_table" data-section="PopFrequency" data-ga-action="ScrollPopFrequency" data-ga-label="popfreq" class="popfreq_table">
|
||
<table id="popfreq_datatable" class="stripe">
|
||
<thead>
|
||
<tr>
|
||
<th title="Continental population name">Population</th>
|
||
<th title="Global (total) and sub-populations">Group</th>
|
||
<th title="Total allele counts by population">Sample Size</th>
|
||
<th title="Reference assembly allele">Ref Allele</th>
|
||
<th title="Alternate allele">Alt Allele</th>
|
||
<th title="Reference Homozygous genotype Frequency">Ref HMOZ</th>
|
||
<th title="Alternate Homozygous genotype Frequency">Alt HMOZ</th>
|
||
<th title="Heterozygous genotype Frequency">HTRZ</th>
|
||
<th title="-Log(HWE Probability)">HWEP</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492705">Total</a>
|
||
|
||
</td>
|
||
<td>Global</td>
|
||
<td class="samp_s">105516</td>
|
||
<td class="popfreq_ref_allele">G=0.285663</td>
|
||
<td class="popfreq_alt_allele">C=0.714337, T=0.000000</td>
|
||
<td class="popfreq_alt_allele">0.094659</td>
|
||
<td class="popfreq_alt_allele">0.523333</td>
|
||
<td class="popfreq_alt_allele">0.382008</td>
|
||
<td class="popfreq_alt_allele">32</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492695">European</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">90388</td>
|
||
<td class="popfreq_ref_allele">G=0.26336</td>
|
||
<td class="popfreq_alt_allele">C=0.73664, T=0.00000</td>
|
||
<td class="popfreq_alt_allele">0.073439</td>
|
||
<td class="popfreq_alt_allele">0.54671</td>
|
||
<td class="popfreq_alt_allele">0.379851</td>
|
||
<td class="popfreq_alt_allele">11</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492703">African</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">2988</td>
|
||
<td class="popfreq_ref_allele">G=0.6854</td>
|
||
<td class="popfreq_alt_allele">C=0.3146, T=0.0000</td>
|
||
<td class="popfreq_alt_allele">0.523427</td>
|
||
<td class="popfreq_alt_allele">0.15261</td>
|
||
<td class="popfreq_alt_allele">0.323963</td>
|
||
<td class="popfreq_alt_allele">32</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492696">African Others</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">132</td>
|
||
<td class="popfreq_ref_allele">G=0.841</td>
|
||
<td class="popfreq_alt_allele">C=0.159, T=0.000</td>
|
||
<td class="popfreq_alt_allele">0.727273</td>
|
||
<td class="popfreq_alt_allele">0.045455</td>
|
||
<td class="popfreq_alt_allele">0.227273</td>
|
||
<td class="popfreq_alt_allele">1</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492698">African American</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">2856</td>
|
||
<td class="popfreq_ref_allele">G=0.6782</td>
|
||
<td class="popfreq_alt_allele">C=0.3218, T=0.0000</td>
|
||
<td class="popfreq_alt_allele">0.514006</td>
|
||
<td class="popfreq_alt_allele">0.157563</td>
|
||
<td class="popfreq_alt_allele">0.328431</td>
|
||
<td class="popfreq_alt_allele">32</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492704">Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">3230</td>
|
||
<td class="popfreq_ref_allele">G=0.4152</td>
|
||
<td class="popfreq_alt_allele">C=0.5848, T=0.0000</td>
|
||
<td class="popfreq_alt_allele">0.185139</td>
|
||
<td class="popfreq_alt_allele">0.354799</td>
|
||
<td class="popfreq_alt_allele">0.460062</td>
|
||
<td class="popfreq_alt_allele">3</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492697">East Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">2594</td>
|
||
<td class="popfreq_ref_allele">G=0.3774</td>
|
||
<td class="popfreq_alt_allele">C=0.6226, T=0.0000</td>
|
||
<td class="popfreq_alt_allele">0.153431</td>
|
||
<td class="popfreq_alt_allele">0.398612</td>
|
||
<td class="popfreq_alt_allele">0.447957</td>
|
||
<td class="popfreq_alt_allele">2</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492701">Other Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">636</td>
|
||
<td class="popfreq_ref_allele">G=0.569</td>
|
||
<td class="popfreq_alt_allele">C=0.431, T=0.000</td>
|
||
<td class="popfreq_alt_allele">0.314465</td>
|
||
<td class="popfreq_alt_allele">0.176101</td>
|
||
<td class="popfreq_alt_allele">0.509434</td>
|
||
<td class="popfreq_alt_allele">0</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492699">Latin American 1</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">668</td>
|
||
<td class="popfreq_ref_allele">G=0.421</td>
|
||
<td class="popfreq_alt_allele">C=0.579, T=0.000</td>
|
||
<td class="popfreq_alt_allele">0.185629</td>
|
||
<td class="popfreq_alt_allele">0.344311</td>
|
||
<td class="popfreq_alt_allele">0.47006</td>
|
||
<td class="popfreq_alt_allele">0</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492700">Latin American 2</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">390</td>
|
||
<td class="popfreq_ref_allele">G=0.341</td>
|
||
<td class="popfreq_alt_allele">C=0.659, T=0.000</td>
|
||
<td class="popfreq_alt_allele">0.205128</td>
|
||
<td class="popfreq_alt_allele">0.523077</td>
|
||
<td class="popfreq_alt_allele">0.271795</td>
|
||
<td class="popfreq_alt_allele">17</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492702">South Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">198</td>
|
||
<td class="popfreq_ref_allele">G=0.566</td>
|
||
<td class="popfreq_alt_allele">C=0.434, T=0.000</td>
|
||
<td class="popfreq_alt_allele">0.323232</td>
|
||
<td class="popfreq_alt_allele">0.191919</td>
|
||
<td class="popfreq_alt_allele">0.484848</td>
|
||
<td class="popfreq_alt_allele">0</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN11605645">Other</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">7654</td>
|
||
<td class="popfreq_ref_allele">G=0.3164</td>
|
||
<td class="popfreq_alt_allele">C=0.6836, T=0.0000</td>
|
||
<td class="popfreq_alt_allele">0.120199</td>
|
||
<td class="popfreq_alt_allele">0.487327</td>
|
||
<td class="popfreq_alt_allele">0.392475</td>
|
||
<td class="popfreq_alt_allele">18</td>
|
||
</tr>
|
||
|
||
</tbody>
|
||
</table>
|
||
|
||
|
||
<br/>
|
||
<br/>
|
||
</div>
|
||
|
||
|
||
<a data-width="640px" href="#frequency_tp"
|
||
ref="section=Frequency&action=Click-on-Tooltip&label=frequency_tp"
|
||
data-section="Frequency" data-ga-action="Click-on-Tooltip"
|
||
data-ga-label="frequency_tp" class="fa fa-question-circle align-right ncbiPopper">
|
||
<span class="usa-sr-only">Help</span>
|
||
</a>
|
||
<p id="frequency_tp">
|
||
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
|
||
</p>
|
||
|
||
|
||
|
||
|
||
<a href="/snp/rs1042522/download/frequency">
|
||
<i class="fa fa-download" aria-hidden="true"></i> Download</a>
|
||
<div id="dbsnp_freq_table">
|
||
<table id="dbsnp_freq_datatable" class="stripe">
|
||
<thead>
|
||
<tr>
|
||
<th class="study_header">Study</th>
|
||
<th class="population_header">Population</th>
|
||
<th>Group</th>
|
||
<th>Sample Size</th>
|
||
<th>Ref Allele</th>
|
||
<th>Alt Allele</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA400167">TopMed</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
Global
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">264690</td>
|
||
<td>G=0.382621</td>
|
||
<td>C=0.617379</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Exomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488253">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">250534</td>
|
||
<td>G=0.331835</td>
|
||
<td>C=0.668165</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Exomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10181265">European</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">135066</td>
|
||
<td>G=0.263493</td>
|
||
<td>C=0.736507</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Exomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
Asian
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">48982</td>
|
||
<td>G=0.47362</td>
|
||
<td>C=0.52638</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Exomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488255">American</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">34568</td>
|
||
<td>G=0.28547</td>
|
||
<td>C=0.71453</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Exomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488254">African</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">15746</td>
|
||
<td>G=0.62009</td>
|
||
<td>C=0.37991</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Exomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488252">Ashkenazi Jewish</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">10076</td>
|
||
<td>G=0.28513</td>
|
||
<td>C=0.71487</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Exomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488248">Other</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">6096</td>
|
||
<td>G=0.3023</td>
|
||
<td>C=0.6977</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488253">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">139992</td>
|
||
<td>G=0.373457</td>
|
||
<td>C=0.626543</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10181265">European</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">75860</td>
|
||
<td>G=0.25788</td>
|
||
<td>C=0.74212</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488254">African</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">41928</td>
|
||
<td>G=0.61057</td>
|
||
<td>C=0.38943</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488255">American</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">13610</td>
|
||
<td>G=0.29743</td>
|
||
<td>C=0.70257</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488252">Ashkenazi Jewish</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">3320</td>
|
||
<td>G=0.2804</td>
|
||
<td>C=0.7196</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488251">East Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">3126</td>
|
||
<td>G=0.4418</td>
|
||
<td>C=0.5582</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA398795">gnomAD - Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488248">Other</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">2148</td>
|
||
<td>G=0.3529</td>
|
||
<td>C=0.6471</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB8661">ExAC</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07490465">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">120924</td>
|
||
<td>G=0.340040</td>
|
||
<td>C=0.659960</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB8661">ExAC</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
Europe
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">73302</td>
|
||
<td>G=0.26589</td>
|
||
<td>C=0.73411</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB8661">ExAC</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
Asian
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">25126</td>
|
||
<td>G=0.47019</td>
|
||
<td>C=0.52981</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB8661">ExAC</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
American
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">11562</td>
|
||
<td>G=0.28853</td>
|
||
<td>C=0.71147</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB8661">ExAC</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
African
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">10030</td>
|
||
<td>G=0.61575</td>
|
||
<td>C=0.38425</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB8661">ExAC</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07486028">Other</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">904</td>
|
||
<td>G=0.335</td>
|
||
<td>C=0.665</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492705">Total</a>
|
||
|
||
</td>
|
||
<td>Global</td>
|
||
<td class="samp_s">105516</td>
|
||
<td>G=0.285663</td>
|
||
<td>C=0.714337, T=0.000000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492695">European</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">90388</td>
|
||
<td>G=0.26336</td>
|
||
<td>C=0.73664, T=0.00000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN11605645">Other</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">7654</td>
|
||
<td>G=0.3164</td>
|
||
<td>C=0.6836, T=0.0000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492704">Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">3230</td>
|
||
<td>G=0.4152</td>
|
||
<td>C=0.5848, T=0.0000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492703">African</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">2988</td>
|
||
<td>G=0.6854</td>
|
||
<td>C=0.3146, T=0.0000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492699">Latin American 1</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">668</td>
|
||
<td>G=0.421</td>
|
||
<td>C=0.579, T=0.000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492700">Latin American 2</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">390</td>
|
||
<td>G=0.341</td>
|
||
<td>C=0.659, T=0.000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA507278">Allele Frequency Aggregator</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492702">South Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">198</td>
|
||
<td>G=0.566</td>
|
||
<td>C=0.434, T=0.000</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA678214">14KJPN</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN16789458">JAPANESE</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">28256</td>
|
||
<td>G=0.34980</td>
|
||
<td>C=0.65020</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA678214">8.3KJPN</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN16789458">JAPANESE</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">16758</td>
|
||
<td>G=0.35523</td>
|
||
<td>C=0.64477</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB31736">1000Genomes_30x</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07490465">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">6404</td>
|
||
<td>G=0.4561</td>
|
||
<td>C=0.5439</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB31736">1000Genomes_30x</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07486022">African</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">1786</td>
|
||
<td>G=0.6674</td>
|
||
<td>C=0.3326</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB31736">1000Genomes_30x</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488239">Europe</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">1266</td>
|
||
<td>G=0.2780</td>
|
||
<td>C=0.7220</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB31736">1000Genomes_30x</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07486027">South Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">1202</td>
|
||
<td>G=0.4908</td>
|
||
<td>C=0.5092</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB31736">1000Genomes_30x</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07486024">East Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">1170</td>
|
||
<td>G=0.4120</td>
|
||
<td>C=0.5880</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB31736">1000Genomes_30x</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488242">American</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">980</td>
|
||
<td>G=0.311</td>
|
||
<td>C=0.689</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB6930">1000Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07490465">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">5008</td>
|
||
<td>G=0.4571</td>
|
||
<td>C=0.5429</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB6930">1000Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07486022">African</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">1322</td>
|
||
<td>G=0.6687</td>
|
||
<td>C=0.3313</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB6930">1000Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07486024">East Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">1008</td>
|
||
<td>G=0.4137</td>
|
||
<td>C=0.5863</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB6930">1000Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488239">Europe</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">1006</td>
|
||
<td>G=0.2853</td>
|
||
<td>C=0.7147</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB6930">1000Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07486027">South Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">978</td>
|
||
<td>G=0.492</td>
|
||
<td>C=0.508</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB6930">1000Genomes</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN07488242">American</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">694</td>
|
||
<td>G=0.317</td>
|
||
<td>C=0.683</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA489787">Genetic variation in the Estonian population</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
Estonian
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">4480</td>
|
||
<td>G=0.3004</td>
|
||
<td>C=0.6996</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB7217">The Avon Longitudinal Study of Parents and Children</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
PARENT AND CHILD COHORT
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">3854</td>
|
||
<td>G=0.2504</td>
|
||
<td>C=0.7496</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB7218">UK 10K study - Twins</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
TWIN COHORT
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">3708</td>
|
||
<td>G=0.2446</td>
|
||
<td>C=0.7554</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA589833">KOREAN population from KRGDB</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
KOREAN
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">2928</td>
|
||
<td>G=0.3446</td>
|
||
<td>A=0.0000, C=0.6554, T=0.0000</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA609628">Korean Genome Project</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
KOREAN
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">1828</td>
|
||
<td>G=0.3638</td>
|
||
<td>C=0.6362</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB37584">CNV burdens in cranial meningiomas</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN15458720">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">790</td>
|
||
<td>G=0.419</td>
|
||
<td>C=0.581</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB37584">CNV burdens in cranial meningiomas</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN15458720">CRM</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">790</td>
|
||
<td>G=0.419</td>
|
||
<td>C=0.581</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13103781">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">668</td>
|
||
<td>G=0.404</td>
|
||
<td>C=0.596</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13097346">PA141824203</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">188</td>
|
||
<td>G=0.681</td>
|
||
<td>C=0.319</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13097344">PA141823664</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">180</td>
|
||
<td>G=0.239</td>
|
||
<td>C=0.761</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13095558">PA136109606</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">170</td>
|
||
<td>G=0.424</td>
|
||
<td>C=0.576</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13097345">PA141823945</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">130</td>
|
||
<td>G=0.208</td>
|
||
<td>C=0.792</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA515199">A Vietnamese Genetic Variation Database</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10744005">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">614</td>
|
||
<td>G=0.505</td>
|
||
<td>C=0.495</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PPRJNA503394">Northern Sweden</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10359154">ACPOP</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">600</td>
|
||
<td>G=0.330</td>
|
||
<td>C=0.670</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB8705">Medical Genome Project healthy controls from Spanish population</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13001620">Spanish controls</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">534</td>
|
||
<td>G=0.283</td>
|
||
<td>C=0.717</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA586841">SGDP_PRJ</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
Global
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">416</td>
|
||
<td>G=0.267</td>
|
||
<td>C=0.733</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">HapMap</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10820145">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">326</td>
|
||
<td>G=0.439</td>
|
||
<td>C=0.561</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">HapMap</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10821182">American</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">120</td>
|
||
<td>G=0.233</td>
|
||
<td>C=0.767</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">HapMap</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10821181">African</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">118</td>
|
||
<td>G=0.669</td>
|
||
<td>C=0.331</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">HapMap</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10821184">Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">88</td>
|
||
<td>G=0.41</td>
|
||
<td>C=0.59</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB7895">FINRISK</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13002954">Finnish from FINRISK project</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">304</td>
|
||
<td>G=0.289</td>
|
||
<td>C=0.711</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA288297">Qatari</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13019808">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">216</td>
|
||
<td>G=0.463</td>
|
||
<td>C=0.537</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB36033">Ancient Sardinia genome-wide 1240k capture data generation and analysis</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN15458807">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">56</td>
|
||
<td>G=0.11</td>
|
||
<td>C=0.89</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA267856">Siberian</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13113809">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">44</td>
|
||
<td>G=0.18</td>
|
||
<td>C=0.82</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJEB7725">The Danish reference pan genome</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13003120">Danish</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">40</td>
|
||
<td>G=0.33</td>
|
||
<td>C=0.68</td>
|
||
</tr>
|
||
|
||
|
||
</tbody>
|
||
</table>
|
||
</div>
|
||
|
||
|
||
</div>
|
||
<div id="variant_details" class="js-tabcontent">
|
||
<a data-width="640px" href="#variant_details_tp"
|
||
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|
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|
||
data-ga-label="variant_details_tp" class="fa fa-question-circle align-right ncbiPopper">
|
||
<span class="usa-sr-only">Help</span>
|
||
</a>
|
||
<p id="variant_details_tp">
|
||
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with <a class="external-link" href="/variation/docs/glossary/#MolCon" rel="nofollow" target="_blank">molecular consequences</a> from <a class="external-link" href="http://www.sequenceontology.org/" rel="nofollow" target="_blank">Sequence Ontology</a>. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.</p>
|
||
|
||
|
||
|
||
|
||
<div>
|
||
|
||
<div class="sect_heading">Genomic Placements</div>
|
||
<div id="gene_plac_allele">
|
||
<!-- display class is a short-cut for specifying the stripe hover order-column
|
||
row-border as the class name for a table -->
|
||
<table id="genomics_placements_table" class="stripe">
|
||
<thead>
|
||
<tr>
|
||
<th>Sequence name</th>
|
||
<th>Change</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 17</td>
|
||
<td>NC_000017.11:g.7676154G>A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 17</td>
|
||
<td>NC_000017.11:g.7676154G>C</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 17</td>
|
||
<td>NC_000017.11:g.7676154G>T</td>
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td>GRCh37.p13 chr 17</td>
|
||
<td>NC_000017.10:g.7579472G>A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh37.p13 chr 17</td>
|
||
<td>NC_000017.10:g.7579472G>C</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh37.p13 chr 17</td>
|
||
<td>NC_000017.10:g.7579472G>T</td>
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td>TP53 RefSeqGene (LRG_321)</td>
|
||
<td>NG_017013.2:g.16397C>T</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>TP53 RefSeqGene (LRG_321)</td>
|
||
<td>NG_017013.2:g.16397C>G</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>TP53 RefSeqGene (LRG_321)</td>
|
||
<td>NG_017013.2:g.16397C>A</td>
|
||
</tr>
|
||
|
||
|
||
</tbody>
|
||
</table>
|
||
</div>
|
||
|
||
|
||
|
||
<div id="trans_anno_allele">
|
||
|
||
|
||
|
||
<div class="sect_heading">
|
||
Gene: <a target="_blank" data-section="Variant Details"
|
||
data-ga-action="Click-on"
|
||
data-ga-label="transcript_annotation_gene_link"
|
||
ref="section=Variant Details&action=Click-on&label=transcript_annotation_gene_link"
|
||
href="/gene/7157">TP53</a>, tumor protein p53
|
||
(minus strand)
|
||
|
||
</div>
|
||
<table class="trans_anno_allele_datatable" class="stripe">
|
||
<thead>
|
||
<tr>
|
||
<th>Molecule type</th>
|
||
<th>Change</th>
|
||
<th>Amino acid[Codon]</th>
|
||
<th>SO Term</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 5</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126115.2:c.
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
|
||
N/A
|
||
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Genic Upstream Transcript Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 6</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126116.2:c.
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
|
||
N/A
|
||
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Genic Upstream Transcript Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 7</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126117.2:c.
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
|
||
N/A
|
||
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Genic Upstream Transcript Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 5</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276697.3:c.
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
|
||
N/A
|
||
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Genic Upstream Transcript Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 6</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276698.3:c.
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
|
||
N/A
|
||
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Genic Upstream Transcript Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 7</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276699.3:c.
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
|
||
N/A
|
||
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Genic Upstream Transcript Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_000546.6:c.215C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > L [</span><span class="codon-ghost">C</span><span class="codon-hilite">T</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform a</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_000537.3:p.Pro72Leu
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > L (Leu)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_000546.6:c.215C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > R [</span><span class="codon-ghost">C</span><span class="codon-hilite">G</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform a</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_000537.3:p.Pro72Arg
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > R (Arg)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_000546.6:c.215C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > H [</span><span class="codon-ghost">C</span><span class="codon-hilite">A</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform a</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_000537.3:p.Pro72His
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > H (His)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276760.3:c.98C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > L [</span><span class="codon-ghost">C</span><span class="codon-hilite">T</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform g</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263689.1:p.Pro33Leu
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > L (Leu)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276760.3:c.98C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > R [</span><span class="codon-ghost">C</span><span class="codon-hilite">G</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform g</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263689.1:p.Pro33Arg
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > R (Arg)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276760.3:c.98C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > H [</span><span class="codon-ghost">C</span><span class="codon-hilite">A</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform g</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263689.1:p.Pro33His
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > H (His)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276761.3:c.98C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > L [</span><span class="codon-ghost">C</span><span class="codon-hilite">T</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform g</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263690.1:p.Pro33Leu
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > L (Leu)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276761.3:c.98C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > R [</span><span class="codon-ghost">C</span><span class="codon-hilite">G</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform g</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263690.1:p.Pro33Arg
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > R (Arg)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276761.3:c.98C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > H [</span><span class="codon-ghost">C</span><span class="codon-hilite">A</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform g</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263690.1:p.Pro33His
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > H (His)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 4</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276695.3:c.98C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > L [</span><span class="codon-ghost">C</span><span class="codon-hilite">T</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform h</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263624.1:p.Pro33Leu
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > L (Leu)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 4</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276695.3:c.98C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > R [</span><span class="codon-ghost">C</span><span class="codon-hilite">G</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform h</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263624.1:p.Pro33Arg
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > R (Arg)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 4</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276695.3:c.98C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > H [</span><span class="codon-ghost">C</span><span class="codon-hilite">A</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform h</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263624.1:p.Pro33His
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > H (His)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 3</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276696.3:c.98C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > L [</span><span class="codon-ghost">C</span><span class="codon-hilite">T</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform i</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263625.1:p.Pro33Leu
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > L (Leu)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 3</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276696.3:c.98C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > R [</span><span class="codon-ghost">C</span><span class="codon-hilite">G</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform i</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263625.1:p.Pro33Arg
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > R (Arg)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 3</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001276696.3:c.98C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > H [</span><span class="codon-ghost">C</span><span class="codon-hilite">A</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform i</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001263625.1:p.Pro33His
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > H (His)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 3</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126114.3:c.215C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > L [</span><span class="codon-ghost">C</span><span class="codon-hilite">T</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform b</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119586.1:p.Pro72Leu
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > L (Leu)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 3</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126114.3:c.215C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > R [</span><span class="codon-ghost">C</span><span class="codon-hilite">G</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform b</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119586.1:p.Pro72Arg
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > R (Arg)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 3</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126114.3:c.215C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > H [</span><span class="codon-ghost">C</span><span class="codon-hilite">A</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform b</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119586.1:p.Pro72His
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > H (His)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 4</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126113.3:c.215C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > L [</span><span class="codon-ghost">C</span><span class="codon-hilite">T</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform c</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119585.1:p.Pro72Leu
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > L (Leu)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 4</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126113.3:c.215C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > R [</span><span class="codon-ghost">C</span><span class="codon-hilite">G</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform c</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119585.1:p.Pro72Arg
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > R (Arg)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 4</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126113.3:c.215C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > H [</span><span class="codon-ghost">C</span><span class="codon-hilite">A</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform c</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119585.1:p.Pro72His
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > H (His)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126112.3:c.215C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > L [</span><span class="codon-ghost">C</span><span class="codon-hilite">T</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform a</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119584.1:p.Pro72Leu
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > L (Leu)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126112.3:c.215C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > R [</span><span class="codon-ghost">C</span><span class="codon-hilite">G</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform a</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119584.1:p.Pro72Arg
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > R (Arg)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126112.3:c.215C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > H [</span><span class="codon-ghost">C</span><span class="codon-hilite">A</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform a</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119584.1:p.Pro72His
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > H (His)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 8</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126118.2:c.98C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > L [</span><span class="codon-ghost">C</span><span class="codon-hilite">T</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform g</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119590.1:p.Pro33Leu
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > L (Leu)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>TP53 transcript variant 8</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126118.2:c.98C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > R [</span><span class="codon-ghost">C</span><span class="codon-hilite">G</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_even">
|
||
<td>cellular tumor antigen p53 isoform g</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119590.1:p.Pro33Arg
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > R (Arg)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>TP53 transcript variant 8</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001126118.2:c.98C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">P [</span><span class="codon-ghost">C</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > H [</span><span class="codon-ghost">C</span><span class="codon-hilite">A</span><span class="codon-ghost">C</span><span class="codon-plain">]</span></span>
|
||
</td>
|
||
<td>
|
||
|
||
Coding Sequence Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="vard_odd">
|
||
<td>cellular tumor antigen p53 isoform g</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001119590.1:p.Pro33His
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
P (Pro) > H (His)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
</tbody>
|
||
</table>
|
||
|
||
|
||
|
||
</div>
|
||
</div>
|
||
|
||
</div>
|
||
|
||
<div id="clinical_significance" class="js-tabcontent">
|
||
<div>
|
||
<a data-width="640px" href="#clin_sig_tp"
|
||
ref="section=Clinical Significance&action=Click-on-Tooltip&label=clinical_significance_tp"
|
||
data-section="Clinical Significance" data-ga-action="Click-on-Tooltip"
|
||
data-ga-label="clinical_significance_tp"
|
||
class="fa fa-question-circle align-right ncbiPopper">
|
||
<span class="usa-sr-only">Help</span>
|
||
</a>
|
||
<p id="clin_sig_tp">
|
||
Clinical Significance tab shows a list of <a class="external-link" href="/clinvar/docs/clinsig" rel="nofollow" target="_blank">clinical significance </a>entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. <a href="/clinvar/RCV000001615.2" rel="nofollow" target="_blank">RCV000001615.2</a>) or Allele ID (i.e. <a href="/clinvar/variation/12274/" rel="nofollow" target="_blank">12274</a>) to access full ClinVar report.</p>
|
||
|
||
|
||
|
||
|
||
<div class="sect_heading">Allele: G= (allele ID:
|
||
<a ref="section=Clinical Significance&action=Click-on&label=allele_link"
|
||
target="_blank" href="/clinvar?term=(176504[AlleleID])"
|
||
data-section="Clinical Significance"
|
||
data-ga-action="Click-on"
|
||
data-ga-label="allele_link">
|
||
176504
|
||
</a>)
|
||
</div>
|
||
|
||
<table id="clinical_significance_datatable" class="stripe" data-height="15em">
|
||
<thead>
|
||
<tr>
|
||
<th>ClinVar Accession</th>
|
||
<th>Disease Names</th>
|
||
<th>Clinical Significance</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV000152112.4">RCV000152112.4</a>
|
||
</td>
|
||
<td>not specified</td>
|
||
<td>Benign</td>
|
||
</tr>
|
||
|
||
</tbody>
|
||
</table>
|
||
|
||
|
||
<div class="sect_heading">Allele: A (allele ID:
|
||
<a ref="section=Clinical Significance&action=Click-on&label=allele_link"
|
||
target="_blank" href="/clinvar?term=(846295[AlleleID])"
|
||
data-section="Clinical Significance"
|
||
data-ga-action="Click-on"
|
||
data-ga-label="allele_link">
|
||
846295
|
||
</a>)
|
||
</div>
|
||
|
||
<table id="clinical_significance_datatable" class="stripe" data-height="15em">
|
||
<thead>
|
||
<tr>
|
||
<th>ClinVar Accession</th>
|
||
<th>Disease Names</th>
|
||
<th>Clinical Significance</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV001071888.3">RCV001071888.3</a>
|
||
</td>
|
||
<td>Li-Fraumeni syndrome</td>
|
||
<td>Uncertain-Significance</td>
|
||
</tr>
|
||
|
||
</tbody>
|
||
</table>
|
||
|
||
|
||
<div class="sect_heading">Allele: C (allele ID:
|
||
<a ref="section=Clinical Significance&action=Click-on&label=allele_link"
|
||
target="_blank" href="/clinvar?term=(27390[AlleleID])"
|
||
data-section="Clinical Significance"
|
||
data-ga-action="Click-on"
|
||
data-ga-label="allele_link">
|
||
27390
|
||
</a>)
|
||
</div>
|
||
|
||
<table id="clinical_significance_datatable" class="stripe" data-height="15em">
|
||
<thead>
|
||
<tr>
|
||
<th>ClinVar Accession</th>
|
||
<th>Disease Names</th>
|
||
<th>Clinical Significance</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV000013144.7">RCV000013144.7</a>
|
||
</td>
|
||
<td>CODON 72 POLYMORPHISM</td>
|
||
<td>Benign</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV000034639.10">RCV000034639.10</a>
|
||
</td>
|
||
<td>not provided</td>
|
||
<td>Benign</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV000079202.19">RCV000079202.19</a>
|
||
</td>
|
||
<td>not specified</td>
|
||
<td>Benign</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV000132165.5">RCV000132165.5</a>
|
||
</td>
|
||
<td>Hereditary cancer-predisposing syndrome</td>
|
||
<td>Benign</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV000144668.8">RCV000144668.8</a>
|
||
</td>
|
||
<td>Li-Fraumeni syndrome 1</td>
|
||
<td>Benign</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV000300782.10">RCV000300782.10</a>
|
||
</td>
|
||
<td>Li-Fraumeni syndrome</td>
|
||
<td>Benign</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV001255631.2">RCV001255631.2</a>
|
||
</td>
|
||
<td>Lip and oral cavity carcinoma</td>
|
||
<td>Pathogenic</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV002225263.2">RCV002225263.2</a>
|
||
</td>
|
||
<td>Hereditary breast ovarian cancer syndrome</td>
|
||
<td>Benign</td>
|
||
</tr>
|
||
|
||
</tbody>
|
||
</table>
|
||
|
||
|
||
<div class="sect_heading">Allele: T (allele ID:
|
||
<a ref="section=Clinical Significance&action=Click-on&label=allele_link"
|
||
target="_blank" href="/clinvar?term=(185405[AlleleID])"
|
||
data-section="Clinical Significance"
|
||
data-ga-action="Click-on"
|
||
data-ga-label="allele_link">
|
||
185405
|
||
</a>)
|
||
</div>
|
||
|
||
<table id="clinical_significance_datatable" class="stripe" data-height="15em">
|
||
<thead>
|
||
<tr>
|
||
<th>ClinVar Accession</th>
|
||
<th>Disease Names</th>
|
||
<th>Clinical Significance</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV000164487.6">RCV000164487.6</a>
|
||
</td>
|
||
<td>Hereditary cancer-predisposing syndrome</td>
|
||
<td>Uncertain-Significance</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV000227427.9">RCV000227427.9</a>
|
||
</td>
|
||
<td>Li-Fraumeni syndrome</td>
|
||
<td>Uncertain-Significance</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="Clinical Significance"
|
||
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
|
||
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
|
||
href="/clinvar/RCV001527080.2">RCV001527080.2</a>
|
||
</td>
|
||
<td>Li-Fraumeni syndrome 1</td>
|
||
<td>Likely-Benign</td>
|
||
</tr>
|
||
|
||
</tbody>
|
||
</table>
|
||
|
||
|
||
|
||
|
||
</div>
|
||
</div>
|
||
|
||
<div id="hgvs_tab" class="js-tabcontent">
|
||
<a data-width="640px" href="#aliases_tp"
|
||
ref="section=HGVS&action=Click-on-Tooltip&label=aliases_tp"
|
||
data-section="HGVS" data-ga-action="Click-on-Tooltip" data-ga-label="aliases_tp"
|
||
class="fa fa-question-circle align-right ncbiPopper">
|
||
<span class="usa-sr-only">Help</span>
|
||
</a>
|
||
<p id="aliases_tp">
|
||
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. <a href="http://varnomen.hgvs.org/">HGVS name</a> is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".</p>
|
||
|
||
<div id="hgvs">
|
||
<table id="alliases_alleles_datatable" class="stripe">
|
||
<thead class="allele_wrap">
|
||
<tr>
|
||
<th>Placement</th>
|
||
|
||
<th>
|
||
G=
|
||
</th>
|
||
|
||
<th>
|
||
A
|
||
</th>
|
||
|
||
<th>
|
||
C
|
||
</th>
|
||
|
||
<th>
|
||
T
|
||
</th>
|
||
|
||
</tr>
|
||
</thead>
|
||
<tbody class="allele_wrap">
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
GRCh38.p14 chr 17
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000017.11:g.7676154=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000017.11:g.7676154G>A
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000017.11:g.7676154G>C
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000017.11:g.7676154G>T
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
GRCh37.p13 chr 17
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000017.10:g.7579472=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000017.10:g.7579472G>A
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000017.10:g.7579472G>C
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000017.10:g.7579472G>T
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 RefSeqGene (LRG_321)
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NG_017013.2:g.16397=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NG_017013.2:g.16397C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NG_017013.2:g.16397C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NG_017013.2:g.16397C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000546.6:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000546.6:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000546.6:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000546.6:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000546.5:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000546.5:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000546.5:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000546.5:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 3
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.3:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.3:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.3:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.3:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 3
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.2:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.2:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.2:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.2:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 3
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276696.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 3
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126114.3:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126114.3:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126114.3:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126114.3:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 3
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126114.2:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126114.2:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126114.2:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126114.2:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 4
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.3:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.3:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.3:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.3:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 4
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.2:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.2:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.2:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.2:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 4
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276695.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 4
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126113.3:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126113.3:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126113.3:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126113.3:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 4
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126113.2:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126113.2:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126113.2:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126113.2:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.3:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.3:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.3:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.3:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.2:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.2:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.2:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.2:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276760.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 2
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.3:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.3:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.3:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.3:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 2
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.2:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.2:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.2:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.2:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 2
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001276761.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 2
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126112.3:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126112.3:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126112.3:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126112.3:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 2
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126112.2:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126112.2:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126112.2:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126112.2:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 8
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126118.2:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126118.2:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126118.2:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126118.2:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 8
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126118.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126118.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126118.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001126118.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 13
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407271.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407271.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407271.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407271.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 13
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407270.1:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407270.1:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407270.1:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407270.1:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 12
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407269.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407269.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407269.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407269.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 12
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407268.1:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407268.1:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407268.1:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407268.1:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 9
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407263.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407263.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407263.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407263.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 9
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407262.1:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407262.1:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407262.1:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407262.1:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 11
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407267.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407267.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407267.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407267.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 11
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407266.1:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407266.1:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407266.1:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407266.1:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 10
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407265.1:c.98=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407265.1:c.98C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407265.1:c.98C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407265.1:c.98C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 10
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407264.1:c.215=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407264.1:c.215C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407264.1:c.215C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001407264.1:c.215C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant 14
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NR_176326.1:n.357=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NR_176326.1:n.357C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NR_176326.1:n.357C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NR_176326.1:n.357C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cellular tumor antigen p53 isoform a
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_000537.3:p.Pro72=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_000537.3:p.Pro72Leu
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_000537.3:p.Pro72Arg
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_000537.3:p.Pro72His
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cellular tumor antigen p53 isoform i
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263625.1:p.Pro33=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263625.1:p.Pro33Leu
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263625.1:p.Pro33Arg
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263625.1:p.Pro33His
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cellular tumor antigen p53 isoform b
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119586.1:p.Pro72=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119586.1:p.Pro72Leu
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119586.1:p.Pro72Arg
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119586.1:p.Pro72His
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cellular tumor antigen p53 isoform h
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263624.1:p.Pro33=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263624.1:p.Pro33Leu
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263624.1:p.Pro33Arg
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263624.1:p.Pro33His
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cellular tumor antigen p53 isoform c
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119585.1:p.Pro72=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119585.1:p.Pro72Leu
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119585.1:p.Pro72Arg
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119585.1:p.Pro72His
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cellular tumor antigen p53 isoform g
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263689.1:p.Pro33=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263689.1:p.Pro33Leu
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263689.1:p.Pro33Arg
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263689.1:p.Pro33His
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cellular tumor antigen p53 isoform g
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263690.1:p.Pro33=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263690.1:p.Pro33Leu
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263690.1:p.Pro33Arg
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001263690.1:p.Pro33His
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cellular tumor antigen p53 isoform a
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119584.1:p.Pro72=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119584.1:p.Pro72Leu
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119584.1:p.Pro72Arg
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119584.1:p.Pro72His
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cellular tumor antigen p53 isoform g
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119590.1:p.Pro33=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119590.1:p.Pro33Leu
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119590.1:p.Pro33Arg
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001119590.1:p.Pro33His
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
TP53 transcript variant X1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
XM_005256778.1:c.176-21=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
XM_005256778.1:c.176-21C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
XM_005256778.1:c.176-21C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
XM_005256778.1:c.176-21C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
</tbody>
|
||
</table>
|
||
</div>
|
||
|
||
</div>
|
||
|
||
<div id="submissions" class="js-tabcontent">
|
||
<a data-width="640px" href="#submissions_tp"
|
||
ref="section=Submissions&action=Click-on-Tooltip&label=submissions_tp"
|
||
data-section="Submissions" data-ga-action="Click-on-Tooltip"
|
||
data-ga-label="submissions_tp" class="fa fa-question-circle align-right ncbiPopper">
|
||
<span class="usa-sr-only">Help</span>
|
||
</a>
|
||
<p id="submissions_tp">
|
||
Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs).
|
||
We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time.
|
||
Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
|
||
</p>
|
||
|
||
|
||
<div class="sect_heading">
|
||
|
||
176 SubSNP,
|
||
|
||
26 Frequency,
|
||
|
||
13 ClinVar
|
||
submissions
|
||
</div>
|
||
<div id="submission">
|
||
<table id="submission_datatable" class="stripe">
|
||
<thead>
|
||
<tr>
|
||
<th>No</th>
|
||
<th>Submitter</th>
|
||
<th>Submission ID</th>
|
||
<th>Date (Build)</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr >
|
||
<td>1</td>
|
||
<td>
|
||
|
||
LEE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1509829">ss1509829</a>
|
||
|
||
</td>
|
||
<td>Oct 05, 2000
|
||
(86)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>2</td>
|
||
<td>
|
||
|
||
HGBASE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2419871">ss2419871</a>
|
||
|
||
</td>
|
||
<td>Nov 14, 2000
|
||
(89)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>3</td>
|
||
<td>
|
||
|
||
SC_JCM
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2463129">ss2463129</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2000
|
||
(89)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>4</td>
|
||
<td>
|
||
|
||
WICVAR
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3176059">ss3176059</a>
|
||
|
||
</td>
|
||
<td>Aug 15, 2001
|
||
(102)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>5</td>
|
||
<td>
|
||
|
||
LEE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss4390694">ss4390694</a>
|
||
|
||
</td>
|
||
<td>May 29, 2002
|
||
(106)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>6</td>
|
||
<td>
|
||
|
||
LEE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss4403906">ss4403906</a>
|
||
|
||
</td>
|
||
<td>May 29, 2002
|
||
(106)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>7</td>
|
||
<td>
|
||
|
||
SNP500CANCER
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5586947">ss5586947</a>
|
||
|
||
</td>
|
||
<td>Mar 31, 2003
|
||
(113)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>8</td>
|
||
<td>
|
||
|
||
WI_SSAHASNP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6876177">ss6876177</a>
|
||
|
||
</td>
|
||
<td>Feb 20, 2003
|
||
(111)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>9</td>
|
||
<td>
|
||
|
||
SC_SNP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss14828256">ss14828256</a>
|
||
|
||
</td>
|
||
<td>Dec 05, 2003
|
||
(119)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>10</td>
|
||
<td>
|
||
|
||
CGAP-GAI
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss16228600">ss16228600</a>
|
||
|
||
</td>
|
||
<td>Feb 27, 2004
|
||
(120)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>11</td>
|
||
<td>
|
||
|
||
CSHL-HAPMAP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss16760078">ss16760078</a>
|
||
|
||
</td>
|
||
<td>Feb 27, 2004
|
||
(120)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>12</td>
|
||
<td>
|
||
|
||
SSAHASNP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss21424619">ss21424619</a>
|
||
|
||
</td>
|
||
<td>Apr 05, 2004
|
||
(121)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>13</td>
|
||
<td>
|
||
|
||
MGC_GENOME_DIFF
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss28497373">ss28497373</a>
|
||
|
||
</td>
|
||
<td>Sep 24, 2004
|
||
(126)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>14</td>
|
||
<td>
|
||
|
||
MGC_GENOME_DIFF
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss28512049">ss28512049</a>
|
||
|
||
</td>
|
||
<td>Sep 24, 2004
|
||
(126)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>15</td>
|
||
<td>
|
||
|
||
EGP_SNPS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss32469466">ss32469466</a>
|
||
|
||
</td>
|
||
<td>Dec 02, 2004
|
||
(126)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>16</td>
|
||
<td>
|
||
|
||
ABI
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss40756430">ss40756430</a>
|
||
|
||
</td>
|
||
<td>Mar 10, 2006
|
||
(126)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>17</td>
|
||
<td>
|
||
|
||
CANCER-GENOME
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss48533626">ss48533626</a>
|
||
|
||
</td>
|
||
<td>Mar 10, 2006
|
||
(126)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>18</td>
|
||
<td>
|
||
|
||
EGP_SNPS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss66856877">ss66856877</a>
|
||
|
||
</td>
|
||
<td>Dec 01, 2006
|
||
(127)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>19</td>
|
||
<td>
|
||
|
||
SI_EXO
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss71641730">ss71641730</a>
|
||
|
||
</td>
|
||
<td>May 18, 2007
|
||
(127)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>20</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss74901666">ss74901666</a>
|
||
|
||
</td>
|
||
<td>Dec 06, 2007
|
||
(129)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>21</td>
|
||
<td>
|
||
|
||
CGM_KYOTO
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss76864481">ss76864481</a>
|
||
|
||
</td>
|
||
<td>Dec 06, 2007
|
||
(129)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>22</td>
|
||
<td>
|
||
|
||
HGSV
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss77368561">ss77368561</a>
|
||
|
||
</td>
|
||
<td>Dec 06, 2007
|
||
(129)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>23</td>
|
||
<td>
|
||
|
||
PHARMGKB_CREATE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss84172835">ss84172835</a>
|
||
|
||
</td>
|
||
<td>Dec 15, 2007
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>24</td>
|
||
<td>
|
||
|
||
PHARMGKB_CREATE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss84172846">ss84172846</a>
|
||
|
||
</td>
|
||
<td>Dec 15, 2007
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>25</td>
|
||
<td>
|
||
|
||
PHARMGKB_CREATE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss84172869">ss84172869</a>
|
||
|
||
</td>
|
||
<td>Dec 15, 2007
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>26</td>
|
||
<td>
|
||
|
||
PHARMGKB_CREATE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss84173063">ss84173063</a>
|
||
|
||
</td>
|
||
<td>Dec 15, 2007
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>27</td>
|
||
<td>
|
||
|
||
BCMHGSC_JDW
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss90524417">ss90524417</a>
|
||
|
||
</td>
|
||
<td>Mar 24, 2008
|
||
(129)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>28</td>
|
||
<td>
|
||
|
||
HUMANGENOME_JCVI
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss96578357">ss96578357</a>
|
||
|
||
</td>
|
||
<td>Feb 06, 2009
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>29</td>
|
||
<td>
|
||
|
||
KFSHRC_RADBIO
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss105111344">ss105111344</a>
|
||
|
||
</td>
|
||
<td>Feb 06, 2009
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>30</td>
|
||
<td>
|
||
|
||
1000GENOMES
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss113260832">ss113260832</a>
|
||
|
||
</td>
|
||
<td>Jan 25, 2009
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>31</td>
|
||
<td>
|
||
|
||
ENSEMBL
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss132645907">ss132645907</a>
|
||
|
||
</td>
|
||
<td>Dec 01, 2009
|
||
(131)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>32</td>
|
||
<td>
|
||
|
||
ENSEMBL
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss136962647">ss136962647</a>
|
||
|
||
</td>
|
||
<td>Dec 01, 2009
|
||
(131)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>33</td>
|
||
<td>
|
||
|
||
SEATTLESEQ
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss159734466">ss159734466</a>
|
||
|
||
</td>
|
||
<td>Dec 01, 2009
|
||
(131)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>34</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss159892412">ss159892412</a>
|
||
|
||
</td>
|
||
<td>Dec 01, 2009
|
||
(131)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>35</td>
|
||
<td>
|
||
|
||
COMPLETE_GENOMICS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss167755102">ss167755102</a>
|
||
|
||
</td>
|
||
<td>Jul 04, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>36</td>
|
||
<td>
|
||
|
||
COMPLETE_GENOMICS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss169011665">ss169011665</a>
|
||
|
||
</td>
|
||
<td>Jul 04, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>37</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss170062384">ss170062384</a>
|
||
|
||
</td>
|
||
<td>Jul 04, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>38</td>
|
||
<td>
|
||
|
||
COMPLETE_GENOMICS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss171135553">ss171135553</a>
|
||
|
||
</td>
|
||
<td>Jul 04, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>39</td>
|
||
<td>
|
||
|
||
BCM-HGSC-SUB
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss208005019">ss208005019</a>
|
||
|
||
</td>
|
||
<td>Jul 04, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>40</td>
|
||
<td>
|
||
|
||
1000GENOMES
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss210907281">ss210907281</a>
|
||
|
||
</td>
|
||
<td>Jul 14, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>41</td>
|
||
<td>
|
||
|
||
1000GENOMES
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss227449846">ss227449846</a>
|
||
|
||
</td>
|
||
<td>Jul 14, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>42</td>
|
||
<td>
|
||
|
||
1000GENOMES
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss237173876">ss237173876</a>
|
||
|
||
</td>
|
||
<td>Jul 15, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>43</td>
|
||
<td>
|
||
|
||
1000GENOMES
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss243485869">ss243485869</a>
|
||
|
||
</td>
|
||
<td>Jul 15, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>44</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss244268863">ss244268863</a>
|
||
|
||
</td>
|
||
<td>Jul 04, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>45</td>
|
||
<td>
|
||
|
||
BL
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss255474801">ss255474801</a>
|
||
|
||
</td>
|
||
<td>May 09, 2011
|
||
(134)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>46</td>
|
||
<td>
|
||
|
||
OMIM-CURATED-RECORDS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss275513802">ss275513802</a>
|
||
|
||
</td>
|
||
<td>Nov 22, 2010
|
||
(133)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>47</td>
|
||
<td>
|
||
|
||
OMICIA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss275516321">ss275516321</a>
|
||
|
||
</td>
|
||
<td>Aug 29, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>48</td>
|
||
<td>
|
||
|
||
GMI
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss282682486">ss282682486</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>49</td>
|
||
<td>
|
||
|
||
PJP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss292010371">ss292010371</a>
|
||
|
||
</td>
|
||
<td>May 09, 2011
|
||
(134)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>50</td>
|
||
<td>
|
||
|
||
NHLBI-ESP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss342443172">ss342443172</a>
|
||
|
||
</td>
|
||
<td>May 09, 2011
|
||
(134)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>51</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss410886683">ss410886683</a>
|
||
|
||
</td>
|
||
<td>Sep 17, 2011
|
||
(135)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>52</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss479263677">ss479263677</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>53</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss479266613">ss479266613</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>54</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss479635493">ss479635493</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>55</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss484432514">ss484432514</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>56</td>
|
||
<td>
|
||
|
||
1000GENOMES
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss491115344">ss491115344</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>57</td>
|
||
<td>
|
||
|
||
EXOME_CHIP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss491516529">ss491516529</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>58</td>
|
||
<td>
|
||
|
||
CLINSEQ_SNP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss491729176">ss491729176</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>59</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss536603957">ss536603957</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>60</td>
|
||
<td>
|
||
|
||
TISHKOFF
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss565152392">ss565152392</a>
|
||
|
||
</td>
|
||
<td>Apr 25, 2013
|
||
(138)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>61</td>
|
||
<td>
|
||
|
||
SSMP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss660940297">ss660940297</a>
|
||
|
||
</td>
|
||
<td>Apr 25, 2013
|
||
(138)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>62</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss778654660">ss778654660</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>63</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss782662723">ss782662723</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>64</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss783631622">ss783631622</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>65</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss831913250">ss831913250</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>66</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss834112538">ss834112538</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>67</td>
|
||
<td>
|
||
|
||
EVA-GONL
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss992899216">ss992899216</a>
|
||
|
||
</td>
|
||
<td>Aug 21, 2014
|
||
(142)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>68</td>
|
||
<td>
|
||
|
||
JMKIDD_LAB
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1067567548">ss1067567548</a>
|
||
|
||
</td>
|
||
<td>Aug 21, 2014
|
||
(142)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>69</td>
|
||
<td>
|
||
|
||
1000GENOMES
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1357813388">ss1357813388</a>
|
||
|
||
</td>
|
||
<td>Aug 21, 2014
|
||
(142)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>70</td>
|
||
<td>
|
||
|
||
DDI
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1427970283">ss1427970283</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>71</td>
|
||
<td>
|
||
|
||
EVA_GENOME_DK
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1578079123">ss1578079123</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>72</td>
|
||
<td>
|
||
|
||
EVA_FINRISK
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1584103859">ss1584103859</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>73</td>
|
||
<td>
|
||
|
||
EVA_UK10K_ALSPAC
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1635240398">ss1635240398</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>74</td>
|
||
<td>
|
||
|
||
EVA_UK10K_TWINSUK
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1678234431">ss1678234431</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>75</td>
|
||
<td>
|
||
|
||
EVA_EXAC
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1692579901">ss1692579901</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>76</td>
|
||
<td>
|
||
|
||
EVA_MGP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1711447010">ss1711447010</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>77</td>
|
||
<td>
|
||
|
||
EVA_SVP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1713568240">ss1713568240</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>78</td>
|
||
<td>
|
||
|
||
CLINVAR
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1751110392">ss1751110392</a>
|
||
|
||
</td>
|
||
<td>May 21, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>79</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1752241679">ss1752241679</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>80</td>
|
||
<td>
|
||
|
||
HAMMER_LAB
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1808692611">ss1808692611</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>81</td>
|
||
<td>
|
||
|
||
WEILL_CORNELL_DGM
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1936345976">ss1936345976</a>
|
||
|
||
</td>
|
||
<td>Feb 12, 2016
|
||
(147)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>82</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1946427495">ss1946427495</a>
|
||
|
||
</td>
|
||
<td>Feb 12, 2016
|
||
(147)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>83</td>
|
||
<td>
|
||
|
||
GENOMED
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1966658571">ss1966658571</a>
|
||
|
||
</td>
|
||
<td>Feb 12, 2016
|
||
(147)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>84</td>
|
||
<td>
|
||
|
||
JJLAB
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2028961088">ss2028961088</a>
|
||
|
||
</td>
|
||
<td>Sep 14, 2016
|
||
(149)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>85</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2094800802">ss2094800802</a>
|
||
|
||
</td>
|
||
<td>Dec 20, 2016
|
||
(150)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>86</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2095071150">ss2095071150</a>
|
||
|
||
</td>
|
||
<td>Dec 20, 2016
|
||
(150)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>87</td>
|
||
<td>
|
||
|
||
USC_VALOUEV
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2157408828">ss2157408828</a>
|
||
|
||
</td>
|
||
<td>Dec 20, 2016
|
||
(150)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>88</td>
|
||
<td>
|
||
|
||
HUMAN_LONGEVITY
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2215319666">ss2215319666</a>
|
||
|
||
</td>
|
||
<td>Dec 20, 2016
|
||
(150)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>89</td>
|
||
<td>
|
||
|
||
SYSTEMSBIOZJU
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2628972669">ss2628972669</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>90</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2633372555">ss2633372555</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>91</td>
|
||
<td>
|
||
|
||
GRF
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2701951520">ss2701951520</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>92</td>
|
||
<td>
|
||
|
||
GNOMAD
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2742410547">ss2742410547</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>93</td>
|
||
<td>
|
||
|
||
GNOMAD
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2749679886">ss2749679886</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>94</td>
|
||
<td>
|
||
|
||
GNOMAD
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2947436379">ss2947436379</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>95</td>
|
||
<td>
|
||
|
||
AFFY
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2985084752">ss2985084752</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>96</td>
|
||
<td>
|
||
|
||
AFFY
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2985722821">ss2985722821</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>97</td>
|
||
<td>
|
||
|
||
SWEGEN
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3015157839">ss3015157839</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>98</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3021752319">ss3021752319</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>99</td>
|
||
<td>
|
||
|
||
EVA_SAMSUNG_MC
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3023070243">ss3023070243</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>100</td>
|
||
<td>
|
||
|
||
BIOINF_KMB_FNS_UNIBA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3028299707">ss3028299707</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>101</td>
|
||
<td>
|
||
|
||
CSHL
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3351641711">ss3351641711</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>102</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3627620219">ss3627620219</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>103</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3631355146">ss3631355146</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>104</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3633134504">ss3633134504</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>105</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3633841584">ss3633841584</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>106</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3634663355">ss3634663355</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>107</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3636353773">ss3636353773</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>108</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3637281050">ss3637281050</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>109</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3638148196">ss3638148196</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>110</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3640370674">ss3640370674</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>111</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3643127588">ss3643127588</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>112</td>
|
||
<td>
|
||
|
||
OMUKHERJEE_ADBS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3646503356">ss3646503356</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>113</td>
|
||
<td>
|
||
|
||
URBANLAB
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3650598904">ss3650598904</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>114</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3652165134">ss3652165134</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>115</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3653857049">ss3653857049</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>116</td>
|
||
<td>
|
||
|
||
EGCUT_WGS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3682123038">ss3682123038</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>117</td>
|
||
<td>
|
||
|
||
EVA_DECODE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3700039781">ss3700039781</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>118</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3725600063">ss3725600063</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>119</td>
|
||
<td>
|
||
|
||
ACPOP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3741852661">ss3741852661</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>120</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3744147021">ss3744147021</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>121</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3744963699">ss3744963699</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>122</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3754421771">ss3754421771</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>123</td>
|
||
<td>
|
||
|
||
ILLUMINA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3772461747">ss3772461747</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>124</td>
|
||
<td>
|
||
|
||
PACBIO
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3788143256">ss3788143256</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>125</td>
|
||
<td>
|
||
|
||
PACBIO
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3793112555">ss3793112555</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>126</td>
|
||
<td>
|
||
|
||
PACBIO
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3797998185">ss3797998185</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>127</td>
|
||
<td>
|
||
|
||
KHV_HUMAN_GENOMES
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3819691776">ss3819691776</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>128</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3825073938">ss3825073938</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>129</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3825531047">ss3825531047</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>130</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3825545821">ss3825545821</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>131</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3825891643">ss3825891643</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>132</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3834767326">ss3834767326</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>133</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3840992140">ss3840992140</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>134</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3846486536">ss3846486536</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>135</td>
|
||
<td>
|
||
|
||
SGDP_PRJ
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3885289740">ss3885289740</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>136</td>
|
||
<td>
|
||
|
||
KRGDB
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3934882622">ss3934882622</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>137</td>
|
||
<td>
|
||
|
||
KOGIC
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3978354151">ss3978354151</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>138</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3983901684">ss3983901684</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>139</td>
|
||
<td>
|
||
|
||
FSA-LAB
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3984106877">ss3984106877</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>140</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3984719666">ss3984719666</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>141</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3985779849">ss3985779849</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>142</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3986072729">ss3986072729</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>143</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3986711521">ss3986711521</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>144</td>
|
||
<td>
|
||
|
||
TOPMED
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5028671105">ss5028671105</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>145</td>
|
||
<td>
|
||
|
||
TOMMO_GENOMICS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5221389427">ss5221389427</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>146</td>
|
||
<td>
|
||
|
||
CPQ_GEN_INCA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5236854173">ss5236854173</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>147</td>
|
||
<td>
|
||
|
||
CPQ_GEN_INCA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5236857891">ss5236857891</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>148</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5236939348">ss5236939348</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>149</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5237237459">ss5237237459</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>150</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5237571702">ss5237571702</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>151</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5237667945">ss5237667945</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>152</td>
|
||
<td>
|
||
|
||
1000G_HIGH_COVERAGE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5302344589">ss5302344589</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>153</td>
|
||
<td>
|
||
|
||
TRAN_CS_UWATERLOO
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5314446554">ss5314446554</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>154</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5426241317">ss5426241317</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>155</td>
|
||
<td>
|
||
|
||
CSS-BFX
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5442110347">ss5442110347</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>156</td>
|
||
<td>
|
||
|
||
HUGCELL_USP
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5495527706">ss5495527706</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>157</td>
|
||
<td>
|
||
|
||
1000G_HIGH_COVERAGE
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5605659524">ss5605659524</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>158</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5623893859">ss5623893859</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>159</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5623969825">ss5623969825</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>160</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5624068491">ss5624068491</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>161</td>
|
||
<td>
|
||
|
||
SANFORD_IMAGENETICS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5624391658">ss5624391658</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>162</td>
|
||
<td>
|
||
|
||
SANFORD_IMAGENETICS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5659676713">ss5659676713</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>163</td>
|
||
<td>
|
||
|
||
TOMMO_GENOMICS
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5776954337">ss5776954337</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>164</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5799457840">ss5799457840</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>165</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5800205776">ss5800205776</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>166</td>
|
||
<td>
|
||
|
||
YY_MCH
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5816315718">ss5816315718</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>167</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5833689547">ss5833689547</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>168</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5847470836">ss5847470836</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>169</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5847787900">ss5847787900</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>170</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5848440272">ss5848440272</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>171</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5851729129">ss5851729129</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>172</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5913134425">ss5913134425</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>173</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5951086951">ss5951086951</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>174</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5979499514">ss5979499514</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>175</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5980950903">ss5980950903</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>176</td>
|
||
<td>
|
||
|
||
EVA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss5981298979">ss5981298979</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>177</td>
|
||
<td>
|
||
|
||
1000Genomes
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>178</td>
|
||
<td>
|
||
|
||
1000Genomes_30x
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.11 - 7676154
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>179</td>
|
||
<td>
|
||
|
||
The Avon Longitudinal Study of Parents and Children
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>180</td>
|
||
<td>
|
||
|
||
Genetic variation in the Estonian population
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>181</td>
|
||
<td>
|
||
|
||
ExAC
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>182</td>
|
||
<td>
|
||
|
||
FINRISK
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>183</td>
|
||
<td>
|
||
|
||
The Danish reference pan genome
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>184</td>
|
||
<td>
|
||
|
||
gnomAD - Genomes
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.11 - 7676154
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>185</td>
|
||
<td>
|
||
|
||
gnomAD - Exomes
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>186</td>
|
||
<td>
|
||
|
||
HapMap
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.11 - 7676154
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>187</td>
|
||
<td>
|
||
|
||
KOREAN population from KRGDB
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>188</td>
|
||
<td>
|
||
|
||
Korean Genome Project
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.11 - 7676154
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>189</td>
|
||
<td>
|
||
|
||
Medical Genome Project healthy controls from Spanish population
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>190</td>
|
||
<td>
|
||
|
||
Northern Sweden
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>191</td>
|
||
<td>
|
||
|
||
Ancient Sardinia genome-wide 1240k capture data generation and analysis
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>192</td>
|
||
<td>
|
||
|
||
CNV burdens in cranial meningiomas
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>193</td>
|
||
<td>
|
||
|
||
PharmGKB Aggregated
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.11 - 7676154
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>194</td>
|
||
<td>
|
||
|
||
Qatari
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>195</td>
|
||
<td>
|
||
|
||
SGDP_PRJ
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>196</td>
|
||
<td>
|
||
|
||
Siberian
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>197</td>
|
||
<td>
|
||
|
||
8.3KJPN
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>198</td>
|
||
<td>
|
||
|
||
14KJPN
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.11 - 7676154
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>199</td>
|
||
<td>
|
||
|
||
TopMed
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.11 - 7676154
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>200</td>
|
||
<td>
|
||
|
||
UK 10K study - Twins
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>201</td>
|
||
<td>
|
||
|
||
A Vietnamese Genetic Variation Database
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.10 - 7579472
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>202</td>
|
||
<td>
|
||
|
||
ALFA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000017.11 - 7676154
|
||
|
||
</td>
|
||
<td>Apr 27, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>203</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV000013144.7/">RCV000013144.7</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>204</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV000034639.10/">RCV000034639.10</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>205</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV000079202.19/">RCV000079202.19</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>206</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV000132165.5/">RCV000132165.5</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>207</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV000144668.8/">RCV000144668.8</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>208</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV000152112.4/">RCV000152112.4</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>209</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV000164487.6/">RCV000164487.6</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>210</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV000227427.9/">RCV000227427.9</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>211</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV000300782.10/">RCV000300782.10</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>212</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV001071888.3/">RCV001071888.3</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>213</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV001255631.2/">RCV001255631.2</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>214</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV001527080.2/">RCV001527080.2</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>215</td>
|
||
<td>
|
||
|
||
ClinVar
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a target="_blank" data-section="Submissions"
|
||
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
|
||
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
|
||
href="/clinvar/RCV002225263.2/">RCV002225263.2</a>
|
||
|
||
</td>
|
||
<td>Oct 17, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
</tbody>
|
||
</table>
|
||
|
||
</div>
|
||
|
||
|
||
</div>
|
||
|
||
<div id="history" class="js-tabcontent">
|
||
<a data-width="640px" href="#history_tp"
|
||
ref="section=History&action=Click-on-Tooltip&label=history_tp"
|
||
data-section="History" data-ga-action="Click-on-Tooltip" data-ga-label="history_tp"
|
||
class="fa fa-question-circle align-right ncbiPopper">
|
||
<span class="usa-sr-only">Help</span>
|
||
</a>
|
||
<p id="history_tp">
|
||
History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).</p>
|
||
|
||
|
||
<div id="updt_hist">
|
||
|
||
|
||
<table id="up_hist_datatable" class="stripe">
|
||
<thead>
|
||
<tr>
|
||
<th>Associated ID</th>
|
||
<th>History Updated (Build)</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
|
||
data-ga-label="Associated_ID_link"
|
||
ref="section=History&action=Click-on&label=Associated_ID_link"
|
||
href="rs2229076">rs2229076</a>
|
||
</td>
|
||
<td>Jan 04, 2002
|
||
(102)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
|
||
data-ga-label="Associated_ID_link"
|
||
ref="section=History&action=Click-on&label=Associated_ID_link"
|
||
href="rs3174747">rs3174747</a>
|
||
</td>
|
||
<td>Jul 03, 2002
|
||
(106)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
|
||
data-ga-label="Associated_ID_link"
|
||
ref="section=History&action=Click-on&label=Associated_ID_link"
|
||
href="rs4134781">rs4134781</a>
|
||
</td>
|
||
<td>Nov 14, 2002
|
||
(109)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
|
||
data-ga-label="Associated_ID_link"
|
||
ref="section=History&action=Click-on&label=Associated_ID_link"
|
||
href="rs17844988">rs17844988</a>
|
||
</td>
|
||
<td>Mar 10, 2006
|
||
(126)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
|
||
data-ga-label="Associated_ID_link"
|
||
ref="section=History&action=Click-on&label=Associated_ID_link"
|
||
href="rs17857747">rs17857747</a>
|
||
</td>
|
||
<td>Mar 10, 2006
|
||
(126)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
|
||
data-ga-label="Associated_ID_link"
|
||
ref="section=History&action=Click-on&label=Associated_ID_link"
|
||
href="rs17882155">rs17882155</a>
|
||
</td>
|
||
<td>Mar 10, 2006
|
||
(126)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" data-section="History" data-ga-action="Click-on"
|
||
data-ga-label="Associated_ID_link"
|
||
ref="section=History&action=Click-on&label=Associated_ID_link"
|
||
href="rs60388830">rs60388830</a>
|
||
</td>
|
||
<td>May 25, 2008
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
</tbody>
|
||
</table>
|
||
</div>
|
||
|
||
|
||
|
||
<div id="obs_present">
|
||
<span>Added to this RefSNP Cluster:</span>
|
||
|
||
|
||
<table id="obs_present_table" class="observation_table stripe">
|
||
<thead>
|
||
<tr>
|
||
<th>Submission IDs</th>
|
||
<th>Observation <a href="/variation/notation/">SPDI</a></th>
|
||
<th>Canonical <a href="/variation/notation/">SPDI</a></th>
|
||
<th>Source RSIDs</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
42060016,
|
||
|
||
ss3934882622
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.10:7579471:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
RCV001071888.3
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
ss77368561,
|
||
|
||
ss90524417,
|
||
|
||
ss113260832,
|
||
|
||
ss159892412,
|
||
|
||
ss167755102,
|
||
|
||
ss169011665,
|
||
|
||
ss171135553,
|
||
|
||
ss208005019,
|
||
|
||
ss210907281,
|
||
|
||
ss244268863,
|
||
|
||
ss255474801,
|
||
|
||
ss282682486,
|
||
|
||
ss292010371,
|
||
|
||
ss479263677,
|
||
|
||
ss491729176,
|
||
|
||
ss1713568240,
|
||
|
||
ss3643127588
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.9:7520196:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
71024053,
|
||
|
||
39391353,
|
||
|
||
27861286,
|
||
|
||
3007675,
|
||
|
||
100320,
|
||
|
||
4284492,
|
||
|
||
11708619,
|
||
|
||
42060016,
|
||
|
||
562770,
|
||
|
||
15137526,
|
||
|
||
1005776,
|
||
|
||
269207,
|
||
|
||
18387898,
|
||
|
||
37306720,
|
||
|
||
9925182,
|
||
|
||
79358734,
|
||
|
||
39391353,
|
||
|
||
8726164,
|
||
|
||
ss227449846,
|
||
|
||
ss237173876,
|
||
|
||
ss243485869,
|
||
|
||
ss342443172,
|
||
|
||
ss479266613,
|
||
|
||
ss479635493,
|
||
|
||
ss484432514,
|
||
|
||
ss491115344,
|
||
|
||
ss491516529,
|
||
|
||
ss536603957,
|
||
|
||
ss565152392,
|
||
|
||
ss660940297,
|
||
|
||
ss778654660,
|
||
|
||
ss782662723,
|
||
|
||
ss783631622,
|
||
|
||
ss831913250,
|
||
|
||
ss834112538,
|
||
|
||
ss992899216,
|
||
|
||
ss1067567548,
|
||
|
||
ss1357813388,
|
||
|
||
ss1427970283,
|
||
|
||
ss1578079123,
|
||
|
||
ss1584103859,
|
||
|
||
ss1635240398,
|
||
|
||
ss1678234431,
|
||
|
||
ss1692579901,
|
||
|
||
ss1711447010,
|
||
|
||
ss1752241679,
|
||
|
||
ss1808692611,
|
||
|
||
ss1936345976,
|
||
|
||
ss1946427495,
|
||
|
||
ss1966658571,
|
||
|
||
ss2028961088,
|
||
|
||
ss2094800802,
|
||
|
||
ss2095071150,
|
||
|
||
ss2157408828,
|
||
|
||
ss2628972669,
|
||
|
||
ss2633372555,
|
||
|
||
ss2701951520,
|
||
|
||
ss2742410547,
|
||
|
||
ss2749679886,
|
||
|
||
ss2947436379,
|
||
|
||
ss2985084752,
|
||
|
||
ss2985722821,
|
||
|
||
ss3015157839,
|
||
|
||
ss3021752319,
|
||
|
||
ss3023070243,
|
||
|
||
ss3351641711,
|
||
|
||
ss3627620219,
|
||
|
||
ss3631355146,
|
||
|
||
ss3633134504,
|
||
|
||
ss3633841584,
|
||
|
||
ss3634663355,
|
||
|
||
ss3636353773,
|
||
|
||
ss3637281050,
|
||
|
||
ss3638148196,
|
||
|
||
ss3640370674,
|
||
|
||
ss3646503356,
|
||
|
||
ss3652165134,
|
||
|
||
ss3653857049,
|
||
|
||
ss3682123038,
|
||
|
||
ss3741852661,
|
||
|
||
ss3744147021,
|
||
|
||
ss3744963699,
|
||
|
||
ss3754421771,
|
||
|
||
ss3772461747,
|
||
|
||
ss3788143256,
|
||
|
||
ss3793112555,
|
||
|
||
ss3797998185,
|
||
|
||
ss3825073938,
|
||
|
||
ss3825531047,
|
||
|
||
ss3825545821,
|
||
|
||
ss3825891643,
|
||
|
||
ss3834767326,
|
||
|
||
ss3840992140,
|
||
|
||
ss3885289740,
|
||
|
||
ss3934882622,
|
||
|
||
ss3983901684,
|
||
|
||
ss3984106877,
|
||
|
||
ss3984719666,
|
||
|
||
ss3985779849,
|
||
|
||
ss3986072729,
|
||
|
||
ss3986711521,
|
||
|
||
ss5221389427,
|
||
|
||
ss5236854173,
|
||
|
||
ss5236857891,
|
||
|
||
ss5237571702,
|
||
|
||
ss5426241317,
|
||
|
||
ss5442110347,
|
||
|
||
ss5623893859,
|
||
|
||
ss5623969825,
|
||
|
||
ss5624068491,
|
||
|
||
ss5624391658,
|
||
|
||
ss5659676713,
|
||
|
||
ss5799457840,
|
||
|
||
ss5800205776,
|
||
|
||
ss5833689547,
|
||
|
||
ss5847470836,
|
||
|
||
ss5847787900,
|
||
|
||
ss5848440272,
|
||
|
||
ss5951086951,
|
||
|
||
ss5979499514,
|
||
|
||
ss5980950903,
|
||
|
||
ss5981298979
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.10:7579471:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
RCV000013144.7,
|
||
|
||
RCV000034639.10,
|
||
|
||
RCV000079202.19,
|
||
|
||
RCV000132165.5,
|
||
|
||
RCV000144668.8,
|
||
|
||
RCV000300782.10,
|
||
|
||
RCV001255631.2,
|
||
|
||
RCV002225263.2,
|
||
|
||
93185459,
|
||
|
||
500820283,
|
||
|
||
1453274,
|
||
|
||
34732152,
|
||
|
||
4685,
|
||
|
||
110791441,
|
||
|
||
244216767,
|
||
|
||
8057383630,
|
||
|
||
ss275513802,
|
||
|
||
ss275516321,
|
||
|
||
ss2215319666,
|
||
|
||
ss3028299707,
|
||
|
||
ss3650598904,
|
||
|
||
ss3700039781,
|
||
|
||
ss3725600063,
|
||
|
||
ss3819691776,
|
||
|
||
ss3846486536,
|
||
|
||
ss3978354151,
|
||
|
||
ss5028671105,
|
||
|
||
ss5236939348,
|
||
|
||
ss5237237459,
|
||
|
||
ss5237667945,
|
||
|
||
ss5302344589,
|
||
|
||
ss5314446554,
|
||
|
||
ss5495527706,
|
||
|
||
ss5605659524,
|
||
|
||
ss5776954337,
|
||
|
||
ss5816315718,
|
||
|
||
ss5851729129,
|
||
|
||
ss5913134425
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
ss14828256,
|
||
|
||
ss16760078,
|
||
|
||
ss21424619
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NT_010718.14:6420477:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
ss1509829,
|
||
|
||
ss2419871,
|
||
|
||
ss2463129,
|
||
|
||
ss3176059,
|
||
|
||
ss4390694,
|
||
|
||
ss4403906,
|
||
|
||
ss5586947,
|
||
|
||
ss6876177,
|
||
|
||
ss16228600,
|
||
|
||
ss28497373,
|
||
|
||
ss28512049,
|
||
|
||
ss32469466,
|
||
|
||
ss40756430,
|
||
|
||
ss48533626,
|
||
|
||
ss66856877,
|
||
|
||
ss71641730,
|
||
|
||
ss74901666,
|
||
|
||
ss76864481,
|
||
|
||
ss84172835,
|
||
|
||
ss84172846,
|
||
|
||
ss84172869,
|
||
|
||
ss84173063,
|
||
|
||
ss96578357,
|
||
|
||
ss105111344,
|
||
|
||
ss132645907,
|
||
|
||
ss136962647,
|
||
|
||
ss159734466,
|
||
|
||
ss170062384,
|
||
|
||
ss410886683
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NT_010718.16:7182845:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
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|
||
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|
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|
||
</td>
|
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|
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|
||
<tr>
|
||
<td>
|
||
|
||
42060016,
|
||
|
||
ss3934882622
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.10:7579471:G:T
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:T
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
RCV000164487.6,
|
||
|
||
RCV000227427.9,
|
||
|
||
RCV001527080.2,
|
||
|
||
8057383630,
|
||
|
||
ss1751110392
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:T
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000017.11:7676153:G:T
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
</tbody>
|
||
</table>
|
||
|
||
|
||
</div>
|
||
|
||
|
||
|
||
|
||
|
||
|
||
|
||
</div>
|
||
<div id="publications" class="js-tabcontent">
|
||
<a data-width="640px" href="#publications_tp"
|
||
ref="section=Publications&action=Click-on-Tooltip&label=publications_tp"
|
||
data-section="Publications" data-ga-action="Click-on-Tooltip"
|
||
data-ga-label="publications_tp" class="fa fa-question-circle align-right ncbiPopper">
|
||
<span class="usa-sr-only">Help</span>
|
||
</a>
|
||
<p id="publications_tp">
|
||
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.</p>
|
||
|
||
|
||
<div class="sect_heading">
|
||
390
|
||
citations for rs1042522
|
||
</div>
|
||
<div id="publication">
|
||
<table id="publication_datatable" class="stripe">
|
||
<thead>
|
||
<tr>
|
||
<th>PMID</th>
|
||
<th class="fir_col">Title</th>
|
||
<th>Author</th>
|
||
<th>Year</th>
|
||
<th>Journal</th>
|
||
</tr>
|
||
</thead>
|
||
<tbody>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/1975675"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">1975675</a>
|
||
</td>
|
||
<td class="fir_col">Codon 72 polymorphism of the TP53 gene.</td>
|
||
<td>Ara S et al.</td>
|
||
<td>1990</td>
|
||
<td>Nucleic acids research</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/1999338"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">1999338</a>
|
||
</td>
|
||
<td class="fir_col">Characterization of a frequent polymorphism in the coding sequence of the Tp53 gene in colonic cancer patients and a control population.</td>
|
||
<td>Olschwang S et al.</td>
|
||
<td>1991</td>
|
||
<td>Human genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/8242752"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">8242752</a>
|
||
</td>
|
||
<td class="fir_col">WAF1, a potential mediator of p53 tumor suppression.</td>
|
||
<td>el-Deiry WS et al.</td>
|
||
<td>1993</td>
|
||
<td>Cell</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/9607760"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">9607760</a>
|
||
</td>
|
||
<td class="fir_col">Role of a p53 polymorphism in the development of human papillomavirus-associated cancer.</td>
|
||
<td>Storey A et al.</td>
|
||
<td>1998</td>
|
||
<td>Nature</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/9891044"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">9891044</a>
|
||
</td>
|
||
<td class="fir_col">Two polymorphic variants of wild-type p53 differ biochemically and biologically.</td>
|
||
<td>Thomas M et al.</td>
|
||
<td>1999</td>
|
||
<td>Molecular and cellular biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/10802655"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">10802655</a>
|
||
</td>
|
||
<td class="fir_col">A common polymorphism acts as an intragenic modifier of mutant p53 behaviour.</td>
|
||
<td>Marin MC et al.</td>
|
||
<td>2000</td>
|
||
<td>Nature genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/11403041"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">11403041</a>
|
||
</td>
|
||
<td class="fir_col">Role of TP53 P72R polymorphism in human papillomavirus associated premalignant laryngeal neoplasm.</td>
|
||
<td>Aaltonen LM et al.</td>
|
||
<td>2001</td>
|
||
<td>Journal of medical genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/12567188"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">12567188</a>
|
||
</td>
|
||
<td class="fir_col">The codon 72 polymorphic variants of p53 have markedly different apoptotic potential.</td>
|
||
<td>Dumont P et al.</td>
|
||
<td>2003</td>
|
||
<td>Nature genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/15355915"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">15355915</a>
|
||
</td>
|
||
<td class="fir_col">p53 polymorphism and age of onset of hereditary nonpolyposis colorectal cancer in a Caucasian population.</td>
|
||
<td>Jones JS et al.</td>
|
||
<td>2004</td>
|
||
<td>Clinical cancer research </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/15450681"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">15450681</a>
|
||
</td>
|
||
<td class="fir_col">Tumor suppressor gene TP53 is genetically associated with schizophrenia in the Chinese population.</td>
|
||
<td>Yang Y et al.</td>
|
||
<td>2004</td>
|
||
<td>Neuroscience letters</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/15564288"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">15564288</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms in XPD and TP53 and mutation in human lung cancer.</td>
|
||
<td>Mechanic LE et al.</td>
|
||
<td>2005</td>
|
||
<td>Carcinogenesis</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/16199549"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">16199549</a>
|
||
</td>
|
||
<td class="fir_col">The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC).</td>
|
||
<td>Krüger S et al.</td>
|
||
<td>2005</td>
|
||
<td>Journal of medical genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/16258005"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">16258005</a>
|
||
</td>
|
||
<td class="fir_col">Impact of the MDM2 SNP309 and p53 Arg72Pro polymorphism on age of tumour onset in Li-Fraumeni syndrome.</td>
|
||
<td>Bougeard G et al.</td>
|
||
<td>2006</td>
|
||
<td>Journal of medical genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/16287156"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">16287156</a>
|
||
</td>
|
||
<td class="fir_col">Genetic polymorphisms in cell cycle regulatory genes MDM2 and TP53 are associated with susceptibility to lung cancer.</td>
|
||
<td>Zhang X et al.</td>
|
||
<td>2006</td>
|
||
<td>Human mutation</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/16465622"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">16465622</a>
|
||
</td>
|
||
<td class="fir_col">Bladder cancer predisposition: a multigenic approach to DNA-repair and cell-cycle-control genes.</td>
|
||
<td>Wu X et al.</td>
|
||
<td>2006</td>
|
||
<td>American journal of human genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/16857995"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">16857995</a>
|
||
</td>
|
||
<td class="fir_col">Risk of non-Hodgkin lymphoma (NHL) in relation to germline variation in DNA repair and related genes.</td>
|
||
<td>Hill DA et al.</td>
|
||
<td>2006</td>
|
||
<td>Blood</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/16964264"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">16964264</a>
|
||
</td>
|
||
<td class="fir_col">iASPP preferentially binds p53 proline-rich region and modulates apoptotic function of codon 72-polymorphic p53.</td>
|
||
<td>Bergamaschi D et al.</td>
|
||
<td>2006</td>
|
||
<td>Nature genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/17096406"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">17096406</a>
|
||
</td>
|
||
<td class="fir_col">Germ-line genetic variation of TP53 in osteosarcoma.</td>
|
||
<td>Savage SA et al.</td>
|
||
<td>2007</td>
|
||
<td>Pediatric blood & cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/17301252"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">17301252</a>
|
||
</td>
|
||
<td class="fir_col">Common genetic variation in TP53 is associated with lung cancer risk and prognosis in African Americans and somatic mutations in lung tumors.</td>
|
||
<td>Mechanic LE et al.</td>
|
||
<td>2007</td>
|
||
<td>Cancer epidemiology, biomarkers & prevention </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/17428325"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">17428325</a>
|
||
</td>
|
||
<td class="fir_col">Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.</td>
|
||
<td>Baynes C et al.</td>
|
||
<td>2007</td>
|
||
<td>Breast cancer research </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/17449902"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">17449902</a>
|
||
</td>
|
||
<td class="fir_col">Genetic variation in TP53 and risk of breast cancer in a population-based case control study.</td>
|
||
<td>Sprague BL et al.</td>
|
||
<td>2007</td>
|
||
<td>Carcinogenesis</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/17535973"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">17535973</a>
|
||
</td>
|
||
<td class="fir_col">Tumor suppressor p53 Arg72Pro polymorphism and longevity, cancer survival, and risk of cancer in the general population.</td>
|
||
<td>Ørsted DD et al.</td>
|
||
<td>2007</td>
|
||
<td>The Journal of experimental medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/17537232"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">17537232</a>
|
||
</td>
|
||
<td class="fir_col">Association of TP53 codon 72 polymorphism and the outcome of adjuvant therapy in breast cancer patients.</td>
|
||
<td>Toyama T et al.</td>
|
||
<td>2007</td>
|
||
<td>Breast cancer research </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/17599946"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">17599946</a>
|
||
</td>
|
||
<td class="fir_col">Association of the TP53 codon 72 polymorphism with colorectal cancer in a Chinese population.</td>
|
||
<td>Zhu ZZ et al.</td>
|
||
<td>2007</td>
|
||
<td>Japanese journal of clinical oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/17624591"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">17624591</a>
|
||
</td>
|
||
<td class="fir_col">Genetic variation of TP53, polycyclic aromatic hydrocarbon-related exposures, and breast cancer risk among women on Long Island, New York.</td>
|
||
<td>Gaudet MM et al.</td>
|
||
<td>2008</td>
|
||
<td>Breast cancer research and treatment</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/17638920"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">17638920</a>
|
||
</td>
|
||
<td class="fir_col">Interaction of P53 Arg72Pro and MDM2 T309G polymorphisms and their associations with risk of gastric cardia cancer.</td>
|
||
<td>Yang M et al.</td>
|
||
<td>2007</td>
|
||
<td>Carcinogenesis</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18191955"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18191955</a>
|
||
</td>
|
||
<td class="fir_col">Correlating observed odds ratios from lung cancer case-control studies to SNP functional scores predicted by bioinformatic tools.</td>
|
||
<td>Zhu Y et al.</td>
|
||
<td>2008</td>
|
||
<td>Mutation research</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18298806"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18298806</a>
|
||
</td>
|
||
<td class="fir_col">Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years.</td>
|
||
<td>Rosenberger A et al.</td>
|
||
<td>2008</td>
|
||
<td>BMC cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18357466"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18357466</a>
|
||
</td>
|
||
<td class="fir_col">Prognostic role of p53 codon 72 polymorphism in gastric cancer patients treated with fluorouracil-based adjuvant chemotherapy.</td>
|
||
<td>Huang ZH et al.</td>
|
||
<td>2008</td>
|
||
<td>Journal of cancer research and clinical oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18433491"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18433491</a>
|
||
</td>
|
||
<td class="fir_col">MDM2 gene SNP309 T/G and p53 gene SNP72 G/C do not influence diffuse large B-cell non-Hodgkin lymphoma onset or survival in central European Caucasians.</td>
|
||
<td>Bittenbring J et al.</td>
|
||
<td>2008</td>
|
||
<td>BMC cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18547414"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18547414</a>
|
||
</td>
|
||
<td class="fir_col">Genotyping panel for assessing response to cancer chemotherapy.</td>
|
||
<td>Dai Z et al.</td>
|
||
<td>2008</td>
|
||
<td>BMC medical genomics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18640487"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18640487</a>
|
||
</td>
|
||
<td class="fir_col">Association of donor inflammation- and apoptosis-related genotypes and delayed allograft function after kidney transplantation.</td>
|
||
<td>Israni AK et al.</td>
|
||
<td>2008</td>
|
||
<td>American journal of kidney diseases </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18678618"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18678618</a>
|
||
</td>
|
||
<td class="fir_col">Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes.</td>
|
||
<td>Gaulton KJ et al.</td>
|
||
<td>2008</td>
|
||
<td>Diabetes</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18715757"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18715757</a>
|
||
</td>
|
||
<td class="fir_col">Genetic associations with schizophrenia: meta-analyses of 12 candidate genes.</td>
|
||
<td>Shi J et al.</td>
|
||
<td>2008</td>
|
||
<td>Schizophrenia research</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18798306"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18798306</a>
|
||
</td>
|
||
<td class="fir_col">Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.</td>
|
||
<td>Pangilinan F et al.</td>
|
||
<td>2008</td>
|
||
<td>American journal of medical genetics. Part A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18805939"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18805939</a>
|
||
</td>
|
||
<td class="fir_col">Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.</td>
|
||
<td>Tempfer CB et al.</td>
|
||
<td>2009</td>
|
||
<td>Human reproduction update</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18820009"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18820009</a>
|
||
</td>
|
||
<td class="fir_col">Possible difference in frequencies of genetic polymorphisms of estrogen receptor alpha, estrogen metabolism and P53 genes between estrogen receptor-positive and -negative breast cancers.</td>
|
||
<td>Hamaguchi M et al.</td>
|
||
<td>2008</td>
|
||
<td>Japanese journal of clinical oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18830263"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18830263</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms in DNA repair and one-carbon metabolism genes and overall survival in diffuse large B-cell lymphoma and follicular lymphoma.</td>
|
||
<td>Wang SS et al.</td>
|
||
<td>2009</td>
|
||
<td>Leukemia</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18854777"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18854777</a>
|
||
</td>
|
||
<td class="fir_col">Germline genetic variations in drug action pathways predict clinical outcomes in advanced lung cancer treated with platinum-based chemotherapy.</td>
|
||
<td>Wu X et al.</td>
|
||
<td>2008</td>
|
||
<td>Pharmacogenetics and genomics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18978339"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18978339</a>
|
||
</td>
|
||
<td class="fir_col">Large-scale evaluation of candidate genes identifies associations between DNA repair and genomic maintenance and development of benzene hematotoxicity.</td>
|
||
<td>Lan Q et al.</td>
|
||
<td>2009</td>
|
||
<td>Carcinogenesis</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/18990748"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">18990748</a>
|
||
</td>
|
||
<td class="fir_col">International Lung Cancer Consortium: pooled analysis of sequence variants in DNA repair and cell cycle pathways.</td>
|
||
<td>Hung RJ et al.</td>
|
||
<td>2008</td>
|
||
<td>Cancer epidemiology, biomarkers & prevention </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19052714"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19052714</a>
|
||
</td>
|
||
<td class="fir_col">TP53 codon 72 polymorphism associated with prognosis in patients with advanced gastric cancer treated with paclitaxel and cisplatin.</td>
|
||
<td>Kim JG et al.</td>
|
||
<td>2009</td>
|
||
<td>Cancer chemotherapy and pharmacology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19193430"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19193430</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms in TP53 and MDM2 combined are associated with high grade endometrial cancer.</td>
|
||
<td>Ashton KA et al.</td>
|
||
<td>2009</td>
|
||
<td>Gynecologic oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19224585"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19224585</a>
|
||
</td>
|
||
<td class="fir_col">Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic.</td>
|
||
<td>Polakova V et al.</td>
|
||
<td>2009</td>
|
||
<td>Human mutation</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19237173"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19237173</a>
|
||
</td>
|
||
<td class="fir_col">Bcl2 -938C/A polymorphism carries increased risk of biochemical recurrence after radical prostatectomy.</td>
|
||
<td>Hirata H et al.</td>
|
||
<td>2009</td>
|
||
<td>The Journal of urology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19276375"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19276375</a>
|
||
</td>
|
||
<td class="fir_col">Single nucleotide polymorphisms in the TP53 region and susceptibility to invasive epithelial ovarian cancer.</td>
|
||
<td>Schildkraut JM et al.</td>
|
||
<td>2009</td>
|
||
<td>Cancer research</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19286843"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19286843</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms of DNA damage response genes in radiation-related and sporadic papillary thyroid carcinoma.</td>
|
||
<td>Akulevich NM et al.</td>
|
||
<td>2009</td>
|
||
<td>Endocrine-related cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19302219"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19302219</a>
|
||
</td>
|
||
<td class="fir_col">p53 Arg72Pro, MDM2 T309G and CCND1 G870A polymorphisms are not associated with susceptibility to esophageal adenocarcinoma.</td>
|
||
<td>Liu G et al.</td>
|
||
<td>2010</td>
|
||
<td>Diseases of the esophagus </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19367277"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19367277</a>
|
||
</td>
|
||
<td class="fir_col">Genetic polymorphisms in DNA repair and damage response genes and late normal tissue complications of radiotherapy for breast cancer.</td>
|
||
<td>Chang-Claude J et al.</td>
|
||
<td>2009</td>
|
||
<td>British journal of cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19423538"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19423538</a>
|
||
</td>
|
||
<td class="fir_col">Common genetic variation in TP53 and risk of human papillomavirus persistence and progression to CIN3/cancer revisited.</td>
|
||
<td>Koshiol J et al.</td>
|
||
<td>2009</td>
|
||
<td>Cancer epidemiology, biomarkers & prevention </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19426493"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19426493</a>
|
||
</td>
|
||
<td class="fir_col">A case-control study on the combined effects of p53 and p73 polymorphisms on head and neck cancer risk in an Italian population.</td>
|
||
<td>Gallì P et al.</td>
|
||
<td>2009</td>
|
||
<td>BMC cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19442035"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19442035</a>
|
||
</td>
|
||
<td class="fir_col">Pharmacogenomics of platinum-based chemotherapy in NSCLC.</td>
|
||
<td>Hildebrandt MA et al.</td>
|
||
<td>2009</td>
|
||
<td>Expert opinion on drug metabolism & toxicology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19470478"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19470478</a>
|
||
</td>
|
||
<td class="fir_col">Single-nucleotide polymorphisms in the p53 pathway regulate fertility in humans.</td>
|
||
<td>Kang HJ et al.</td>
|
||
<td>2009</td>
|
||
<td>Proceedings of the National Academy of Sciences of the United States of America</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19471604"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19471604</a>
|
||
</td>
|
||
<td class="fir_col">Lack of association between p53 gene polymorphisms and primary open angle glaucoma in the Japanese population.</td>
|
||
<td>Mabuchi F et al.</td>
|
||
<td>2009</td>
|
||
<td>Molecular vision</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19482343"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19482343</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms in HPV E6/E7 protein interacted genes and risk of cervical cancer in Chinese women: a case-control analysis.</td>
|
||
<td>Zhou X et al.</td>
|
||
<td>2009</td>
|
||
<td>Gynecologic oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19505915"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19505915</a>
|
||
</td>
|
||
<td class="fir_col">Association of genetic polymorphisms, mRNA expression of p53 and p21 with chronic benzene poisoning in a chinese occupational population.</td>
|
||
<td>Sun P et al.</td>
|
||
<td>2009</td>
|
||
<td>Cancer epidemiology, biomarkers & prevention </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19521721"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19521721</a>
|
||
</td>
|
||
<td class="fir_col">Accelerated decline in lung function in cigarette smokers is associated with TP53/MDM2 polymorphisms.</td>
|
||
<td>Hancox RJ et al.</td>
|
||
<td>2009</td>
|
||
<td>Human genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19542078"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19542078</a>
|
||
</td>
|
||
<td class="fir_col">TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li-Fraumeni syndrome: impact on age at first diagnosis.</td>
|
||
<td>Marcel V et al.</td>
|
||
<td>2009</td>
|
||
<td>Journal of medical genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19625214"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19625214</a>
|
||
</td>
|
||
<td class="fir_col">TP53 codon 72 polymorphism and cervical cancer: a pooled analysis of individual data from 49 studies.</td>
|
||
<td>Klug SJ et al.</td>
|
||
<td>2009</td>
|
||
<td>The Lancet. Oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19657586"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19657586</a>
|
||
</td>
|
||
<td class="fir_col">Association study between P53 and P73 gene polymorphisms and the sporadic late-onset form of Alzheimer's disease.</td>
|
||
<td>Scacchi R et al.</td>
|
||
<td>2009</td>
|
||
<td>Journal of neural transmission (Vienna, Austria </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19707196"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19707196</a>
|
||
</td>
|
||
<td class="fir_col">The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.</td>
|
||
<td>Sinilnikova OM et al.</td>
|
||
<td>2009</td>
|
||
<td>British journal of cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19750108"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19750108</a>
|
||
</td>
|
||
<td class="fir_col">Decreased PM10 exposure attenuates age-related lung function decline: genetic variants in p53, p21, and CCND1 modify this effect.</td>
|
||
<td>Imboden M et al.</td>
|
||
<td>2009</td>
|
||
<td>Environmental health perspectives</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19784392"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19784392</a>
|
||
</td>
|
||
<td class="fir_col">Primary open angle glaucoma in a Caucasian population is associated with the p53 codon 72 polymorphism.</td>
|
||
<td>Daugherty CL et al.</td>
|
||
<td>2009</td>
|
||
<td>Molecular vision</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/19786980"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">19786980</a>
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<td class="fir_col">Genetic polymorphisms and the efficacy and toxicity of cisplatin-based chemotherapy in ovarian cancer patients.</td>
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<td>Khrunin AV et al.</td>
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<td>The pharmacogenomics journal</td>
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<td><a target="_blank" href="/pubmed/19822020"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">19822020</a>
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<td class="fir_col">Genetic factors associated with intestinal metaplasia in a high risk Singapore-Chinese population: a cohort study.</td>
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<td>Zhu F et al.</td>
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<td>2009</td>
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<td>BMC gastroenterology</td>
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<td><a target="_blank" href="/pubmed/19826048"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">19826048</a>
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<td class="fir_col">Candidate gene association study of esophageal squamous cell carcinoma in a high-risk region in Iran.</td>
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<td>Akbari MR et al.</td>
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<tr>
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<td><a target="_blank" href="/pubmed/19834951"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">19834951</a>
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</td>
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<td class="fir_col">The Li-Fraumeni syndrome (LFS): a model for the initiation of p53 signatures in the distal Fallopian tube.</td>
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<td>Xian W et al.</td>
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<td>2010</td>
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<td>The Journal of pathology</td>
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<tr>
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<td><a target="_blank" href="/pubmed/19837266"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">19837266</a>
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</td>
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<td class="fir_col">TP53 R72P and MDM2 SNP309 polymorphisms in modification of childhood acute lymphoblastic leukemia susceptibility.</td>
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<td>Do TN et al.</td>
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<td>2009</td>
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<td>Cancer genetics and cytogenetics</td>
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<tr>
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<td><a target="_blank" href="/pubmed/19911060"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">19911060</a>
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<td class="fir_col">Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.</td>
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<td>Doi N et al.</td>
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<tr>
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<td><a target="_blank" href="/pubmed/20003265"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">20003265</a>
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</td>
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<td class="fir_col">Extent of differential allelic expression of candidate breast cancer genes is similar in blood and breast.</td>
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<td>Maia AT et al.</td>
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<td><a target="_blank" href="/pubmed/20100738"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">20100738</a>
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<td class="fir_col">Prevalence and persistence of chromosomal damage and susceptible genotypes of metabolic and DNA repair genes in Chinese vinyl chloride-exposed workers.</td>
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<td>Ji F et al.</td>
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<td>Carcinogenesis</td>
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<tr>
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<td><a target="_blank" href="/pubmed/20110284"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">20110284</a>
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</td>
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<td class="fir_col">Genotype and haplotype analysis of TP53 gene and the risk of pancreatic cancer: an association study in the Czech Republic.</td>
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<td>Naccarati A et al.</td>
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<td>2010</td>
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<td>Carcinogenesis</td>
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<tr>
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<td><a target="_blank" href="/pubmed/20127253"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">20127253</a>
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<td class="fir_col">The role of TP53 and p21 gene polymorphisms in breast cancer biology in a well specified and characterized German cohort.</td>
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<td>Ebner F et al.</td>
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<td>Journal of cancer research and clinical oncology</td>
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<td><a target="_blank" href="/pubmed/20200430"
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data-ga-label="PMID_link">20200430</a>
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<td class="fir_col">TP53, MDM2, NQO1, and susceptibility to cervical cancer.</td>
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<td>Hu X et al.</td>
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<td><a target="_blank" href="/pubmed/20232390"
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data-ga-label="PMID_link">20232390</a>
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<td class="fir_col">Genetic variations of DNA repair genes and their prognostic significance in patients with acute myeloid leukemia.</td>
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<td><a target="_blank" href="/pubmed/20357201"
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<td class="fir_col">Association of polymorphisms of tumor necrosis factor and tumor protein p53 with primary open-angle glaucoma.</td>
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<td><a target="_blank" href="/pubmed/20436704"
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<td class="fir_col">TP53 mutations in Korean patients with non-small cell lung cancer.</td>
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<td>Lee EB et al.</td>
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<td><a target="_blank" href="/pubmed/20452958"
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<td class="fir_col">Single-nucleotide polymorphisms in the p53 signaling pathway.</td>
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<td><a target="_blank" href="/pubmed/20455025"
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<td class="fir_col">Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation.</td>
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<td><a target="_blank" href="/pubmed/20512840"
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data-section="Publications" data-ga-action="Click-on"
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<td class="fir_col">Association between TP53 gene ARG72PRO polymorphism and chromosome aberrations in human cancers.</td>
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<td>Litviakov NV et al.</td>
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<td><a target="_blank" href="/pubmed/20520810"
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data-section="Publications" data-ga-action="Click-on"
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<td class="fir_col">Effects of MDM2, MDM4 and TP53 codon 72 polymorphisms on cancer risk in a cohort study of carriers of TP53 germline mutations.</td>
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<td><a target="_blank" href="/pubmed/20587610"
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data-ga-label="PMID_link">20587610</a>
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<td class="fir_col">Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.</td>
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<td>Molecular human reproduction</td>
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<td><a target="_blank" href="/pubmed/20593380"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">20593380</a>
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<td class="fir_col">p53 Pro72Arg polymorphism and prostate cancer in men of African descent.</td>
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<td>Ricks-Santi L et al.</td>
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<td>The Prostate</td>
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<td><a target="_blank" href="/pubmed/20638924"
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<td class="fir_col">Distribution of TYMS, MTHFR, p53 and MDR1 gene polymorphisms in patients with breast cancer treated with neoadjuvant chemotherapy.</td>
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<td>Henríquez-Hernández LA et al.</td>
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<td class="fir_col">Genotyping of DNA samples isolated from formalin-fixed paraffin-embedded tissues using preamplification.</td>
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<td class="fir_col">Single-nucleotide polymorphisms in p53 pathway and aggressiveness of prostate cancer in a Caucasian population.</td>
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<td class="fir_col">A novel functional DEC1 promoter polymorphism -249T>C reduces risk of squamous cell carcinoma of the head and neck.</td>
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<td class="fir_col">Genomic DNA extraction from whole blood stored from 15- to 30-years at -20 °C by rapid phenol-chloroform protocol: a useful tool for genetic epidemiology studies.</td>
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<td class="fir_col">TP53 polymorphisms in gliomas from Indian patients: Study of codon 72 genotype, rs1642785, rs1800370 and 16 base pair insertion in intron-3.</td>
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<td class="fir_col">Association between polymorphisms in RAPGEF1, TP53, NRF1 and type 2 diabetes in Chinese Han population.</td>
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<td class="fir_col">TP53 codon 72 polymorphism is associated with coronary artery disease in Chilean subjects.</td>
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<td class="fir_col">Studies of the association of Arg72Pro of tumor suppressor protein p53 with type 2 diabetes in a combined analysis of 55,521 Europeans.</td>
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<td class="fir_col">Regulation of female reproduction by p53 and its family members.</td>
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<td class="fir_col">Using epidemiology and genomics to understand osteosarcoma etiology.</td>
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|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21656578"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21656578</a>
|
||
</td>
|
||
<td class="fir_col">Effects of MDM2 promoter polymorphisms and p53 codon 72 polymorphism on risk and age at onset of squamous cell carcinoma of the head and neck.</td>
|
||
<td>Yu H et al.</td>
|
||
<td>2011</td>
|
||
<td>Molecular carcinogenesis</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21672450"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21672450</a>
|
||
</td>
|
||
<td class="fir_col">Is there a biological plausability for p53 codon 72 polymorphism influence on cervical cancer development?</td>
|
||
<td>Sousa H et al.</td>
|
||
<td>2011</td>
|
||
<td>Acta medica portuguesa</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21708280"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21708280</a>
|
||
</td>
|
||
<td class="fir_col">Candidate gene studies in gallbladder cancer: a systematic review and meta-analysis.</td>
|
||
<td>Srivastava K et al.</td>
|
||
<td>2011</td>
|
||
<td>Mutation research</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21741128"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21741128</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Arg72Pro polymorphism in Turkish patients with sporadic amyotrophic lateral sclerosis.</td>
|
||
<td>Ergul E et al.</td>
|
||
<td>2011</td>
|
||
<td>Neurobiology of aging</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21779510"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21779510</a>
|
||
</td>
|
||
<td class="fir_col">Regulation of Fertility by the p53 Family Members.</td>
|
||
<td>Hu W et al.</td>
|
||
<td>2011</td>
|
||
<td>Genes & cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21790896"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21790896</a>
|
||
</td>
|
||
<td class="fir_col">Genetic and environmental predictors, endogenous hormones and growth factors, and risk of estrogen receptor-positive breast cancer in Japanese women.</td>
|
||
<td>Yoshimoto N et al.</td>
|
||
<td>2011</td>
|
||
<td>Cancer science</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21810023"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21810023</a>
|
||
</td>
|
||
<td class="fir_col">Coordination of TP53 abnormalities in breast cancer: data from analysis of TP53 polymorphisms, loss of heterozygosity, methylation, and mutations.</td>
|
||
<td>Denisov EV et al.</td>
|
||
<td>2011</td>
|
||
<td>Genetic testing and molecular biomarkers</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21838531"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21838531</a>
|
||
</td>
|
||
<td class="fir_col">Crosstalk between the FGFR2 and TP53 genes in breast cancer: data from an association study and epistatic interaction analysis.</td>
|
||
<td>Cherdyntseva NV et al.</td>
|
||
<td>2012</td>
|
||
<td>DNA and cell biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21841506"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21841506</a>
|
||
</td>
|
||
<td class="fir_col">Combined effect of genetic polymorphisms in P53, P73, and MDM2 on non-small cell lung cancer survival.</td>
|
||
<td>Liu L et al.</td>
|
||
<td>2011</td>
|
||
<td>Journal of thoracic oncology </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21877955"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21877955</a>
|
||
</td>
|
||
<td class="fir_col">Involvement of single-nucleotide polymorphisms in predisposition to head and neck cancer in Saudi Arabia.</td>
|
||
<td>Al-Hadyan KS et al.</td>
|
||
<td>2012</td>
|
||
<td>Genetic testing and molecular biomarkers</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21897271"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21897271</a>
|
||
</td>
|
||
<td class="fir_col">Analysis of 4 single-nucleotide polymorphisms in relation to cervical dysplasia and cancer development using a high-throughput ligation-detection reaction procedure.</td>
|
||
<td>von Keyserling H et al.</td>
|
||
<td>2011</td>
|
||
<td>International journal of gynecological cancer </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21931130"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21931130</a>
|
||
</td>
|
||
<td class="fir_col">WDR36 and P53 gene variants and susceptibility to primary open-angle glaucoma: analysis of gene-gene interactions.</td>
|
||
<td>Blanco-Marchite C et al.</td>
|
||
<td>2011</td>
|
||
<td>Investigative ophthalmology & visual science</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21946351"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21946351</a>
|
||
</td>
|
||
<td class="fir_col">A germline variant in the TP53 polyadenylation signal confers cancer susceptibility.</td>
|
||
<td>Stacey SN et al.</td>
|
||
<td>2011</td>
|
||
<td>Nature genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22076708"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22076708</a>
|
||
</td>
|
||
<td class="fir_col">Validation of genetic sequence variants as prognostic factors in early-stage head and neck squamous cell cancer survival.</td>
|
||
<td>Azad AK et al.</td>
|
||
<td>2012</td>
|
||
<td>Clinical cancer research </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22178231"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22178231</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms of TP53 are markers of bladder cancer vulnerability and prognosis.</td>
|
||
<td>Lin HY et al.</td>
|
||
<td>2013</td>
|
||
<td>Urologic oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22188361"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22188361</a>
|
||
</td>
|
||
<td class="fir_col">Pharmacogenomics of cisplatin-based chemotherapy in ovarian cancer patients of different ethnic origins.</td>
|
||
<td>Khrunin A et al.</td>
|
||
<td>2012</td>
|
||
<td>Pharmacogenomics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22189267"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22189267</a>
|
||
</td>
|
||
<td class="fir_col">Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time.</td>
|
||
<td>Reiling E et al.</td>
|
||
<td>2012</td>
|
||
<td>European journal of human genetics </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22194650"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22194650</a>
|
||
</td>
|
||
<td class="fir_col">Myocilin mutations among POAG patients from two populations of Tamil Nadu, South India, a comparative analysis.</td>
|
||
<td>Rose R et al.</td>
|
||
<td>2011</td>
|
||
<td>Molecular vision</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22215955"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22215955</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms associated with the risk of lung cancer in a healthy Mexican Mestizo population: Application of the additive model for cancer.</td>
|
||
<td>Pérez-Morales R et al.</td>
|
||
<td>2011</td>
|
||
<td>Genetics and molecular biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22251423"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22251423</a>
|
||
</td>
|
||
<td class="fir_col">NAMPT (visfatin) and AKT1 genetic variants associate with myocardial infarction.</td>
|
||
<td>Leander K et al.</td>
|
||
<td>2012</td>
|
||
<td>Clinica chimica acta; international journal of clinical chemistry</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22294769"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22294769</a>
|
||
</td>
|
||
<td class="fir_col">Mutations and polymorphisms in TP53 gene--an overview on the role in colorectal cancer.</td>
|
||
<td>Naccarati A et al.</td>
|
||
<td>2012</td>
|
||
<td>Mutagenesis</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22300735"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22300735</a>
|
||
</td>
|
||
<td class="fir_col">Genetic predisposition factors and nasopharyngeal carcinoma risk: a review of epidemiological association studies, 2000-2011: Rosetta Stone for NPC: genetics, viral infection, and other environmental factors.</td>
|
||
<td>Hildesheim A et al.</td>
|
||
<td>2012</td>
|
||
<td>Seminars in cancer biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22336942"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22336942</a>
|
||
</td>
|
||
<td class="fir_col">Investigation of the effect of MDM2 SNP309 and TP53 Arg72Pro polymorphisms on the age of onset of cutaneous melanoma.</td>
|
||
<td>Cotignola J et al.</td>
|
||
<td>2012</td>
|
||
<td>The Journal of investigative dermatology</td>
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||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22417303"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22417303</a>
|
||
</td>
|
||
<td class="fir_col">Infrequent p53 gene mutation but UV gradient-like p53 protein positivity in keloids.</td>
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||
<td>Heitzer E et al.</td>
|
||
<td>2012</td>
|
||
<td>Experimental dermatology</td>
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||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22655231"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22655231</a>
|
||
</td>
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||
<td class="fir_col">Sequence Variants and the Risk of Head and Neck Cancer: Pooled Analysis in the INHANCE Consortium.</td>
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||
<td>Chuang SC et al.</td>
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||
<td>2011</td>
|
||
<td>Frontiers in oncology</td>
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||
</tr>
|
||
|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/22703879"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22703879</a>
|
||
</td>
|
||
<td class="fir_col">Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.</td>
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<td>Johnston JJ et al.</td>
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||
<td>2012</td>
|
||
<td>American journal of human genetics</td>
|
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</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22729912"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22729912</a>
|
||
</td>
|
||
<td class="fir_col">Individual and combined effects of MDM2 SNP309 and TP53 Arg72Pro on breast cancer risk: an updated meta-analysis.</td>
|
||
<td>Cheng H et al.</td>
|
||
<td>2012</td>
|
||
<td>Molecular biology reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22742565"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22742565</a>
|
||
</td>
|
||
<td class="fir_col">Germline prognostic markers for urinary bladder cancer: obstacles and opportunities.</td>
|
||
<td>Chang DW et al.</td>
|
||
<td>2012</td>
|
||
<td>Urologic oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22744426"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22744426</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms in TP53 and MDM2 contribute to higher risk of colorectal cancer in Chinese population: a hospital-based, case-control study.</td>
|
||
<td>Zhang Y et al.</td>
|
||
<td>2012</td>
|
||
<td>Molecular biology reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22773013"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22773013</a>
|
||
</td>
|
||
<td class="fir_col">Genetic variants in TP53 and MDM2 associated with male infertility in Chinese population.</td>
|
||
<td>Huang C et al.</td>
|
||
<td>2012</td>
|
||
<td>Asian journal of andrology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22829934"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22829934</a>
|
||
</td>
|
||
<td class="fir_col">Assessment of TP53 mutations in benign and malignant salivary gland neoplasms.</td>
|
||
<td>Gomes CC et al.</td>
|
||
<td>2012</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22879966"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22879966</a>
|
||
</td>
|
||
<td class="fir_col">Systematic testing of literature reported genetic variation associated with coronary restenosis: results of the GENDER Study.</td>
|
||
<td>Verschuren JJ et al.</td>
|
||
<td>2012</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22892830"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22892830</a>
|
||
</td>
|
||
<td class="fir_col">Role of p53 codon 72 polymorphism in chromosomal aberrations and mitotic index in patients with chronic hepatitis B.</td>
|
||
<td>Akbaş H et al.</td>
|
||
<td>2012</td>
|
||
<td>Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22962577"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22962577</a>
|
||
</td>
|
||
<td class="fir_col">Re-evaluation of the carcinogenic significance of hepatitis B virus integration in hepatocarcinogenesis.</td>
|
||
<td>Jiang S et al.</td>
|
||
<td>2012</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22992668"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22992668</a>
|
||
</td>
|
||
<td class="fir_col">Pharmacogenomics knowledge for personalized medicine.</td>
|
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<td>Whirl-Carrillo M et al.</td>
|
||
<td>2012</td>
|
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<td>Clinical pharmacology and therapeutics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23029260"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23029260</a>
|
||
</td>
|
||
<td class="fir_col">p53 codon 72 polymorphism and hematological cancer risk: an update meta-analysis.</td>
|
||
<td>Weng Y et al.</td>
|
||
<td>2012</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23056405"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23056405</a>
|
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</td>
|
||
<td class="fir_col">Predicting the functional effect of amino acid substitutions and indels.</td>
|
||
<td>Choi Y et al.</td>
|
||
<td>2012</td>
|
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<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23072573"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23072573</a>
|
||
</td>
|
||
<td class="fir_col">Multiplex allele-specific amplification from whole blood for detecting multiple polymorphisms simultaneously.</td>
|
||
<td>Zhu J et al.</td>
|
||
<td>2013</td>
|
||
<td>Genetic testing and molecular biomarkers</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23124483"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23124483</a>
|
||
</td>
|
||
<td class="fir_col">Correlation of telomere length shortening with TP53 somatic mutations, polymorphisms and allelic loss in breast tumors and esophageal cancer.</td>
|
||
<td>Hao XD et al.</td>
|
||
<td>2013</td>
|
||
<td>Oncology reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23125046"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23125046</a>
|
||
</td>
|
||
<td class="fir_col">TP53*P72 allele influences negatively female life expectancy in a population of central Italy: cross-sectional study and genetic-demographic approach analysis.</td>
|
||
<td>Di Pietro F et al.</td>
|
||
<td>2013</td>
|
||
<td>The journals of gerontology. Series A, Biological sciences and medical sciences</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23127113"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23127113</a>
|
||
</td>
|
||
<td class="fir_col">Molecular evidence for the bi-clonal origin of neuroendocrine tumor derived metastases.</td>
|
||
<td>Rinner B et al.</td>
|
||
<td>2012</td>
|
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<td>BMC genomics</td>
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</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23168575"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23168575</a>
|
||
</td>
|
||
<td class="fir_col">Candidate gene linkage approach to identify DNA variants that predispose to preterm birth.</td>
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||
<td>Bream EN et al.</td>
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||
<td>2013</td>
|
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<td>Pediatric research</td>
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</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23192612"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23192612</a>
|
||
</td>
|
||
<td class="fir_col">Association of common WRAP 53 variant with ovarian cancer risk in the Polish population.</td>
|
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<td>Mędrek K et al.</td>
|
||
<td>2013</td>
|
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<td>Molecular biology reports</td>
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</tr>
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||
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23207172"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23207172</a>
|
||
</td>
|
||
<td class="fir_col">The p53 codon 72 polymorphism (rs1042522) is associated with proliferative vitreoretinopathy: the Retina 4 Project.</td>
|
||
<td>Pastor-Idoate S et al.</td>
|
||
<td>2013</td>
|
||
<td>Ophthalmology</td>
|
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</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23210739"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23210739</a>
|
||
</td>
|
||
<td class="fir_col">Association of MDM2 and p53 polymorphisms with the advancement of cervical carcinoma.</td>
|
||
<td>Singhal P et al.</td>
|
||
<td>2013</td>
|
||
<td>DNA and cell biology</td>
|
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</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23267696"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23267696</a>
|
||
</td>
|
||
<td class="fir_col">Association of genetic polymorphisms with chronic obstructive pulmonary disease in the Chinese Han population: a case-control study.</td>
|
||
<td>Guo Y et al.</td>
|
||
<td>2012</td>
|
||
<td>BMC medical genomics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23311506"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23311506</a>
|
||
</td>
|
||
<td class="fir_col">The association of a variant in the cell cycle control gene CCND1 and obesity on the development of asthma in the Swiss SAPALDIA study.</td>
|
||
<td>Thun GA et al.</td>
|
||
<td>2013</td>
|
||
<td>The Journal of asthma </td>
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</tr>
|
||
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23360829"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23360829</a>
|
||
</td>
|
||
<td class="fir_col">Association between polymorphisms in the genes for tumor suppressor protein p53 and its regulator NAD(P)H: quinone oxidoreductase 1 (NQO1) and schizophrenia in a Syrian study cohort.</td>
|
||
<td>Lajin B et al.</td>
|
||
<td>2013</td>
|
||
<td>Archives of medical research</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23423487"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23423487</a>
|
||
</td>
|
||
<td class="fir_col">Effect of TP53 codon 72 and MDM2 SNP309 polymorphisms on survival of gastric cancer among patients who receiving 5-fluorouracil-based postoperative adjuvant chemotherapy.</td>
|
||
<td>Wang S et al.</td>
|
||
<td>2013</td>
|
||
<td>Cancer chemotherapy and pharmacology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23552518"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23552518</a>
|
||
</td>
|
||
<td class="fir_col">An identical, complex TP53 mutation arising independently in two unrelated families with diverse cancer profiles: the complexity of interpreting cancer risk in carriers.</td>
|
||
<td>Pinto EM et al.</td>
|
||
<td>2012</td>
|
||
<td>Oncogenesis</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23624782"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23624782</a>
|
||
</td>
|
||
<td class="fir_col">Association of MDM2 SNP309 and TP53 Arg72Pro polymorphisms with risk of endometrial cancer.</td>
|
||
<td>Yoneda T et al.</td>
|
||
<td>2013</td>
|
||
<td>Oncology reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23632240"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23632240</a>
|
||
</td>
|
||
<td class="fir_col">Promoter polymorphisms of pri-miR-34b/c are associated with hepatocellular carcinoma.</td>
|
||
<td>Son MS et al.</td>
|
||
<td>2013</td>
|
||
<td>Gene</td>
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</tr>
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23653000"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23653000</a>
|
||
</td>
|
||
<td class="fir_col">CXCL12 and TP53 genetic polymorphisms as markers of susceptibility in a Brazilian children population with acute lymphoblastic leukemia (ALL).</td>
|
||
<td>de Lourdes Perim A et al.</td>
|
||
<td>2013</td>
|
||
<td>Molecular biology reports</td>
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</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23697595"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23697595</a>
|
||
</td>
|
||
<td class="fir_col">SNPs in genes implicated in radiation response are associated with radiotoxicity and evoke roles as predictive and prognostic biomarkers.</td>
|
||
<td>Alsbeih G et al.</td>
|
||
<td>2013</td>
|
||
<td>Radiation oncology (London, England)</td>
|
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</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23729685"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23729685</a>
|
||
</td>
|
||
<td class="fir_col">Genotype misclassification in genetic association studies of the rs1042522 TP53 (Arg72Pro) polymorphism: a systematic review of studies of breast, lung, colorectal, ovarian, and endometrial cancer.</td>
|
||
<td>Dahabreh IJ et al.</td>
|
||
<td>2013</td>
|
||
<td>American journal of epidemiology</td>
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</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23744327"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23744327</a>
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||
</td>
|
||
<td class="fir_col">[Association of P53 gene polymorphisms with susceptibility to endometriosis].</td>
|
||
<td>Huang Y et al.</td>
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||
<td>2013</td>
|
||
<td>Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23757202"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
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||
data-ga-label="PMID_link">23757202</a>
|
||
</td>
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||
<td class="fir_col">Free the data: one laboratory's approach to knowledge-based genomic variant classification and preparation for EMR integration of genomic data.</td>
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<td>Bean LJ et al.</td>
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||
<td>2013</td>
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||
<td>Human mutation</td>
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</tr>
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||
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23820649"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">23820649</a>
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</td>
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<td class="fir_col">Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.</td>
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<td>Cooper DN et al.</td>
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||
<td>2013</td>
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<td>Human genetics</td>
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</tr>
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<tr>
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||
<td><a target="_blank" href="/pubmed/23837945"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23837945</a>
|
||
</td>
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||
<td class="fir_col">Association of p53 and MDM2 polymorphisms with risk of human papillomavirus (HPV)-related esophageal squamous cell carcinoma (ESCC).</td>
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||
<td>Yang J et al.</td>
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||
<td>2013</td>
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||
<td>Cancer epidemiology</td>
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/23887774"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
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||
data-ga-label="PMID_link">23887774</a>
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</td>
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<td class="fir_col">ACMG clinical laboratory standards for next-generation sequencing.</td>
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<td>Rehm HL et al.</td>
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<td>2013</td>
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||
<td>Genetics in medicine </td>
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/23906684"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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||
data-ga-label="PMID_link">23906684</a>
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<td class="fir_col">Genetic associations with coronary heart disease: meta-analyses of 12 candidate genetic variants.</td>
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<td>Ye H et al.</td>
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||
<td>2013</td>
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<td>Gene</td>
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||
<td><a target="_blank" href="/pubmed/23946381"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">23946381</a>
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<td class="fir_col">Genetic variants associated with colorectal cancer risk: comprehensive research synopsis, meta-analysis, and epidemiological evidence.</td>
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<td>Ma X et al.</td>
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<td>2014</td>
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<td>Gut</td>
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||
<td><a target="_blank" href="/pubmed/24033266"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">24033266</a>
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<td class="fir_col">A systematic approach to assessing the clinical significance of genetic variants.</td>
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<td>Duzkale H et al.</td>
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<td>2013</td>
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<td>Clinical genetics</td>
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<tr>
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||
<td><a target="_blank" href="/pubmed/24084248"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
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||
data-ga-label="PMID_link">24084248</a>
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||
</td>
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||
<td class="fir_col">The GSTM1null (deletion) and MGMT84 rs12917 (Phe/Phe) haplotype are associated with bulky DNA adduct levels in human leukocytes.</td>
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<td>Molina E et al.</td>
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<td>2013</td>
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<td>Mutation research. Genetic toxicology and environmental mutagenesis</td>
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<tr>
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<td><a target="_blank" href="/pubmed/24115240"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">24115240</a>
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</td>
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<td class="fir_col">TP53 single nucleotide polymorphism rs1042522 in salivary gland neoplasms.</td>
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<td>Gomes CC et al.</td>
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||
<td>2014</td>
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<td>Head & neck</td>
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<td><a target="_blank" href="/pubmed/24218030"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">24218030</a>
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<td class="fir_col">Replication of breast cancer susceptibility loci in whites and African Americans using a Bayesian approach.</td>
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<td>O'Brien KM et al.</td>
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<td>2014</td>
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<td>American journal of epidemiology</td>
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<td><a target="_blank" href="/pubmed/24266512"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">24266512</a>
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<td class="fir_col">Association between TP53 gene Arg72Pro polymorphism and idiopathic infertility in southeast Chinese Han males.</td>
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<td>Jin Q et al.</td>
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<td>2013</td>
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<td>Systems biology in reproductive medicine</td>
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||
<td><a target="_blank" href="/pubmed/24369748"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">24369748</a>
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<td class="fir_col">TP53 genetic polymorphisms, interactions with lifestyle factors and lung cancer risk: a case control study in a Chinese population.</td>
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<td>Li Y et al.</td>
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<td>2013</td>
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<td>BMC cancer</td>
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<tr>
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<td><a target="_blank" href="/pubmed/24370206"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">24370206</a>
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<td class="fir_col">Risk genes in head and neck cancer: a systematic review and meta-analysis of last 5 years.</td>
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<td>Brunotto M et al.</td>
|
||
<td>2014</td>
|
||
<td>Oral oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24435975"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24435975</a>
|
||
</td>
|
||
<td class="fir_col">p53 signaling pathway polymorphisms associated to recurrent pregnancy loss.</td>
|
||
<td>Fraga LR et al.</td>
|
||
<td>2014</td>
|
||
<td>Molecular biology reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24491308"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24491308</a>
|
||
</td>
|
||
<td class="fir_col">Systematic review and meta-analysis of candidate gene association studies of lower urinary tract symptoms in men.</td>
|
||
<td>Cartwright R et al.</td>
|
||
<td>2014</td>
|
||
<td>European urology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24534481"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24534481</a>
|
||
</td>
|
||
<td class="fir_col">Association between TLR2, MTR, MTRR, XPC, TP73, TP53 genetic polymorphisms and gastric cancer: a meta-analysis.</td>
|
||
<td>Cheng C et al.</td>
|
||
<td>2014</td>
|
||
<td>Clinics and research in hepatology and gastroenterology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24586820"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24586820</a>
|
||
</td>
|
||
<td class="fir_col">Evidence for an epistatic effect between TP53 R72P and MDM2 T309G SNPs in HIV infection: a cross-sectional study in women from South Brazil.</td>
|
||
<td>Hartwig FP et al.</td>
|
||
<td>2014</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24632578"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24632578</a>
|
||
</td>
|
||
<td class="fir_col">Combined effects of genetic variants of the PTEN, AKT1, MDM2 and p53 genes on the risk of nasopharyngeal carcinoma.</td>
|
||
<td>Zhang X et al.</td>
|
||
<td>2014</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24654968"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24654968</a>
|
||
</td>
|
||
<td class="fir_col">Germline genetics of the p53 pathway affect longevity in a gender specific manner.</td>
|
||
<td>Groß S et al.</td>
|
||
<td>2014</td>
|
||
<td>Current aging science</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24710610"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24710610</a>
|
||
</td>
|
||
<td class="fir_col">No association of the p53 codon 72 polymorphism with malaria in Ghanaian primiparae and Rwandan children.</td>
|
||
<td>Gai PP et al.</td>
|
||
<td>2014</td>
|
||
<td>The American journal of tropical medicine and hygiene</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24728327"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24728327</a>
|
||
</td>
|
||
<td class="fir_col">Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing.</td>
|
||
<td>Bodian DL et al.</td>
|
||
<td>2014</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24818791"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24818791</a>
|
||
</td>
|
||
<td class="fir_col">Genetic variation in the TP53 pathway and bladder cancer risk. a comprehensive analysis.</td>
|
||
<td>Pineda S et al.</td>
|
||
<td>2014</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24820515"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24820515</a>
|
||
</td>
|
||
<td class="fir_col">p21 rs3176352 G>C and p73 rs1801173 C>T polymorphisms are associated with an increased risk of esophageal cancer in a Chinese population.</td>
|
||
<td>Zheng L et al.</td>
|
||
<td>2014</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24863946"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24863946</a>
|
||
</td>
|
||
<td class="fir_col">No evidence of correlation between p53 codon 72 G > C gene polymorphism and cancer risk in Indian population: a meta-analysis.</td>
|
||
<td>Mandal RK et al.</td>
|
||
<td>2014</td>
|
||
<td>Tumour biology </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24944790"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24944790</a>
|
||
</td>
|
||
<td class="fir_col">Screening for 392 polymorphisms in 141 pharmacogenes.</td>
|
||
<td>Kim JY et al.</td>
|
||
<td>2014</td>
|
||
<td>Biomedical reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/24944814"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">24944814</a>
|
||
</td>
|
||
<td class="fir_col">Association between p16(CDKN2A) C540G polymorphism and tumor behavior in prolactinoma: A single-center study.</td>
|
||
<td>Cander S et al.</td>
|
||
<td>2014</td>
|
||
<td>Biomedical reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25060098"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25060098</a>
|
||
</td>
|
||
<td class="fir_col">Association between a single nucleotide polymorphism in the TP53 region and risk of ovarian cancer.</td>
|
||
<td>Xi Y et al.</td>
|
||
<td>2014</td>
|
||
<td>Cell biochemistry and biophysics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25105660"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25105660</a>
|
||
</td>
|
||
<td class="fir_col">Computational screening and molecular dynamic simulation of breast cancer associated deleterious non-synonymous single nucleotide polymorphisms in TP53 gene.</td>
|
||
<td>Chitrala KN et al.</td>
|
||
<td>2014</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25203442"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25203442</a>
|
||
</td>
|
||
<td class="fir_col">The functional TP53 rs1042522 and MDM4 rs4245739 genetic variants contribute to Non-Hodgkin lymphoma risk.</td>
|
||
<td>Fan C et al.</td>
|
||
<td>2014</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25214541"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25214541</a>
|
||
</td>
|
||
<td class="fir_col">A systematic review and meta-analysis of somatic and germline DNA sequence biomarkers of esophageal cancer survival, therapy response and stage.</td>
|
||
<td>Findlay JM et al.</td>
|
||
<td>2015</td>
|
||
<td>Annals of oncology </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25316267"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25316267</a>
|
||
</td>
|
||
<td class="fir_col">TP53 and MDM2 polymorphisms and the risk of endometrial cancer in postmenopausal women.</td>
|
||
<td>Zając A et al.</td>
|
||
<td>2014</td>
|
||
<td>Medical oncology (Northwood, London, England)</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25412941"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25412941</a>
|
||
</td>
|
||
<td class="fir_col">Association between polymorphisms in tumor suppressor genes and oncogenes and risk of hepatocellular carcinoma: a case-control study in an HCC epidemic area within the Han Chinese population.</td>
|
||
<td>Su C et al.</td>
|
||
<td>2014</td>
|
||
<td>Medical oncology (Northwood, London, England)</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25479941"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25479941</a>
|
||
</td>
|
||
<td class="fir_col">Genetic association of single nucleotide polymorphisms in P53 pathway with gastric cancer risk in a Chinese Han population.</td>
|
||
<td>Wu GC et al.</td>
|
||
<td>2015</td>
|
||
<td>Medical oncology (Northwood, London, England)</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25514803"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25514803</a>
|
||
</td>
|
||
<td class="fir_col">Targeted next-generation sequencing of cancer genes in advanced stage malignant pleural mesothelioma: a retrospective study.</td>
|
||
<td>Lo Iacono M et al.</td>
|
||
<td>2015</td>
|
||
<td>Journal of thoracic oncology </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25591549"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25591549</a>
|
||
</td>
|
||
<td class="fir_col">Genetic polymorphisms and gene-dosage effect in ovarian cancer risk and response to paclitaxel/cisplatin chemotherapy.</td>
|
||
<td>Tecza K et al.</td>
|
||
<td>2015</td>
|
||
<td>Journal of experimental & clinical cancer research </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25719551"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25719551</a>
|
||
</td>
|
||
<td class="fir_col">The role of genotypes that modify the toxicity of chemical mutagens in the risk for myeloproliferative neoplasms.</td>
|
||
<td>Gross-Davis CA et al.</td>
|
||
<td>2015</td>
|
||
<td>International journal of environmental research and public health</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25734904"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25734904</a>
|
||
</td>
|
||
<td class="fir_col">Impact of TP53 codon 72 and MDM2 SNP 309 polymorphisms in pancreatic ductal adenocarcinoma.</td>
|
||
<td>Hori Y et al.</td>
|
||
<td>2015</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25741868"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25741868</a>
|
||
</td>
|
||
<td class="fir_col">Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.</td>
|
||
<td>Richards S et al.</td>
|
||
<td>2015</td>
|
||
<td>Genetics in medicine </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25747431"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25747431</a>
|
||
</td>
|
||
<td class="fir_col">No association of TP53 codon 72 SNP with male infertility: a study in a Chinese population and a meta-analysis.</td>
|
||
<td>Chan Y et al.</td>
|
||
<td>2015</td>
|
||
<td>Systems biology in reproductive medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25819169"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25819169</a>
|
||
</td>
|
||
<td class="fir_col">Meta-analysis of association between the TP53 Arg72Pro polymorphism and risk of endometriosis based on case-control studies.</td>
|
||
<td>Yan Y et al.</td>
|
||
<td>2015</td>
|
||
<td>European journal of obstetrics, gynecology, and reproductive biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25881102"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25881102</a>
|
||
</td>
|
||
<td class="fir_col">Genetic variability in drug transport, metabolism or DNA repair affecting toxicity of chemotherapy in ovarian cancer.</td>
|
||
<td>Lambrechts S et al.</td>
|
||
<td>2015</td>
|
||
<td>BMC pharmacology & toxicology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25889195"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25889195</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Arg72Pro polymorphism (rs1042522) and risk of endometriosis among Asian and Caucasian populations.</td>
|
||
<td>Li J et al.</td>
|
||
<td>2015</td>
|
||
<td>European journal of obstetrics, gynecology, and reproductive biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26025918"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26025918</a>
|
||
</td>
|
||
<td class="fir_col">MDM2 and P53 polymorphisms contribute together to the risk and survival of prostate cancer.</td>
|
||
<td>Xue L et al.</td>
|
||
<td>2016</td>
|
||
<td>Oncotarget</td>
|
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</tr>
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|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26099726"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
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||
data-ga-label="PMID_link">26099726</a>
|
||
</td>
|
||
<td class="fir_col">Fuzzy clustering demonstrates that codon 72 SNP rs1042522 of TP53 gene associated with HNSCC but not with prognoses.</td>
|
||
<td>Pinheiro UB et al.</td>
|
||
<td>2015</td>
|
||
<td>Tumour biology </td>
|
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</tr>
|
||
|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26130668"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">26130668</a>
|
||
</td>
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||
<td class="fir_col">Nucleotide Excision Repair Gene ERCC2 and ERCC5 Variants Increase Risk of Uterine Cervical Cancer.</td>
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<td>Joo J et al.</td>
|
||
<td>2016</td>
|
||
<td>Cancer research and treatment</td>
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</tr>
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|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26226484"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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||
data-ga-label="PMID_link">26226484</a>
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||
</td>
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||
<td class="fir_col">Genotype and Haplotype Analyses of TP53 Gene in Breast Cancer Patients: Association with Risk and Clinical Outcomes.</td>
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||
<td>Vymetalkova V et al.</td>
|
||
<td>2015</td>
|
||
<td>PloS one</td>
|
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</tr>
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||
|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26289323"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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||
data-ga-label="PMID_link">26289323</a>
|
||
</td>
|
||
<td class="fir_col">Association of p53 rs1042522, MDM2 rs2279744, and p21 rs1801270 polymorphisms with retinoblastoma risk and invasion in a Chinese population.</td>
|
||
<td>Chen R et al.</td>
|
||
<td>2015</td>
|
||
<td>Scientific reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26305668"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26305668</a>
|
||
</td>
|
||
<td class="fir_col">The Relationship between Vascular Endothelial Growth Factor 1154G/A Polymorphism and Recurrent Implantation Failure.</td>
|
||
<td>Vagnini LD et al.</td>
|
||
<td>2015</td>
|
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<td>Medical principles and practice </td>
|
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</tr>
|
||
|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26382048"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26382048</a>
|
||
</td>
|
||
<td class="fir_col">Genetic Variations in the TP53 Pathway in Native Americans Strongly Suggest Adaptation to the High Altitudes of the Andes.</td>
|
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<td>Jacovas VC et al.</td>
|
||
<td>2015</td>
|
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<td>PloS one</td>
|
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26451011"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26451011</a>
|
||
</td>
|
||
<td class="fir_col">Systematic meta-analyses and field synopsis of genetic association studies in colorectal adenomas.</td>
|
||
<td>Montazeri Z et al.</td>
|
||
<td>2016</td>
|
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<td>International journal of epidemiology</td>
|
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26666818"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26666818</a>
|
||
</td>
|
||
<td class="fir_col">Breast cancer risk in relation to TP53 codon 72 and CDH1 gene polymorphisms in the Bangladeshi women.</td>
|
||
<td>Shabnaz S et al.</td>
|
||
<td>2016</td>
|
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<td>Tumour biology </td>
|
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</tr>
|
||
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26683024"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26683024</a>
|
||
</td>
|
||
<td class="fir_col">Comparison of Genetic Variants in Cancer-Related Genes between Chinese Hui and Han Populations.</td>
|
||
<td>Tian C et al.</td>
|
||
<td>2015</td>
|
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<td>PloS one</td>
|
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26690118"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26690118</a>
|
||
</td>
|
||
<td class="fir_col">An Updated Review on the Genetics of Primary Open Angle Glaucoma.</td>
|
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<td>Abu-Amero K et al.</td>
|
||
<td>2015</td>
|
||
<td>International journal of molecular sciences</td>
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26696550"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26696550</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Codon 72 Polymorphism Predicts Efficacy of Paclitaxel Plus Capecitabine Chemotherapy in Advanced Gastric Cancer Patients.</td>
|
||
<td>Zha Y et al.</td>
|
||
<td>2016</td>
|
||
<td>Archives of medical research</td>
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</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26867771"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26867771</a>
|
||
</td>
|
||
<td class="fir_col">The MDM4 SNP34091 (rs4245739) C-allele is associated with increased risk of ovarian-but not endometrial cancer.</td>
|
||
<td>Gansmo LB et al.</td>
|
||
<td>2016</td>
|
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<td>Tumour biology </td>
|
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</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26870349"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26870349</a>
|
||
</td>
|
||
<td class="fir_col">Impact of single-nucleotide polymorphisms on radiation pneumonitis in cancer patients.</td>
|
||
<td>Guo CX et al.</td>
|
||
<td>2016</td>
|
||
<td>Molecular and clinical oncology</td>
|
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</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26873362"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26873362</a>
|
||
</td>
|
||
<td class="fir_col">Gene Polymorphism Association with Type 2 Diabetes and Related Gene-Gene and Gene-Environment Interactions in a Uyghur Population.</td>
|
||
<td>Xiao S et al.</td>
|
||
<td>2016</td>
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<td>Medical science monitor </td>
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</tr>
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||
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<tr>
|
||
<td><a target="_blank" href="/pubmed/26887047"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26887047</a>
|
||
</td>
|
||
<td class="fir_col">Retrospective study testing next generation sequencing of selected cancer-associated genes in resected prostate cancer.</td>
|
||
<td>Lo Iacono M et al.</td>
|
||
<td>2016</td>
|
||
<td>Oncotarget</td>
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</tr>
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||
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26900293"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26900293</a>
|
||
</td>
|
||
<td class="fir_col">Mutation analysis of 13 driver genes of colorectal cancer-related pathways in Taiwanese patients.</td>
|
||
<td>Chang YC et al.</td>
|
||
<td>2016</td>
|
||
<td>World journal of gastroenterology</td>
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</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26902998"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26902998</a>
|
||
</td>
|
||
<td class="fir_col">The role of WWOX polymorphisms on COPD susceptibility and pulmonary function traits in Chinese: a case-control study and family-based analysis.</td>
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||
<td>Xie C et al.</td>
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||
<td>2016</td>
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<td>Scientific reports</td>
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</tr>
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||
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<tr>
|
||
<td><a target="_blank" href="/pubmed/27223485"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27223485</a>
|
||
</td>
|
||
<td class="fir_col">Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil.</td>
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||
<td>Palmero EI et al.</td>
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||
<td>2016</td>
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<td>Genetics and molecular biology</td>
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/27246533"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27246533</a>
|
||
</td>
|
||
<td class="fir_col">The study of the relation of DNA repair pathway genes SNPs and the sensitivity to radiotherapy and chemotherapy of NSCLC.</td>
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||
<td>Wang C et al.</td>
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||
<td>2016</td>
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<td>Scientific reports</td>
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</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/27248495"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27248495</a>
|
||
</td>
|
||
<td class="fir_col">Study of Association between Pre-Senile Cataracts and the Polymorphisms rs2228000 in XPC and rs1042522 in p53 in Spanish Population.</td>
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<td>López Valverde G et al.</td>
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<td>2016</td>
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<td>PloS one</td>
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/27277665"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27277665</a>
|
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</td>
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||
<td class="fir_col">Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh population.</td>
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<td>Zholdybayeva EV et al.</td>
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<td>2016</td>
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<td>Human genomics</td>
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/27282582"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27282582</a>
|
||
</td>
|
||
<td class="fir_col">TP53 codon 72 polymorphism predicts chronic myeloid leukemia susceptibility and treatment outcome.</td>
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||
<td>Weich N et al.</td>
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||
<td>2016</td>
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<td>Blood cells, molecules & diseases</td>
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/27376129"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27376129</a>
|
||
</td>
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<td class="fir_col">Independent Replication of Published Germline Polymorphisms Associated with Urinary Bladder Cancer Prognosis and Treatment Response.</td>
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<td>Grotenhuis AJ et al.</td>
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<td>2016</td>
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<td>Bladder cancer (Amsterdam, Netherlands)</td>
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</tr>
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<tr>
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<td><a target="_blank" href="/pubmed/27414035"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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||
data-ga-label="PMID_link">27414035</a>
|
||
</td>
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||
<td class="fir_col">Genetic Variants in the p14ARF/MDM2/TP53 Pathway Are Associated with the Prognosis of Esophageal Squamous Cell Carcinoma Patients Treated with Radical Resection.</td>
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<td>Li J et al.</td>
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<td>2016</td>
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<td>PloS one</td>
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<tr>
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<td><a target="_blank" href="/pubmed/27415837"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27415837</a>
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</td>
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<td class="fir_col">Cervical Cancer Genetic Susceptibility: A Systematic Review and Meta-Analyses of Recent Evidence.</td>
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<td>Martínez-Nava GA et al.</td>
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<td>2016</td>
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<td>PloS one</td>
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</tr>
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<tr>
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||
<td><a target="_blank" href="/pubmed/27436625"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">27436625</a>
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</td>
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<td class="fir_col">The Arg72 variant of the p53 functional polymorphism (rs1042522) is associated with coronary artery disease in young South Africans of Indian ancestry.</td>
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<td>Khan S et al.</td>
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<td>2016</td>
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<td>Gene</td>
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||
<td><a target="_blank" href="/pubmed/27506496"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27506496</a>
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||
</td>
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||
<td class="fir_col">A Functional Polymorphism (rs937283) in the MDM2 Promoter Region is Associated with Poor Prognosis of Retinoblastoma in Chinese Han Population.</td>
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<td>Jiao Y et al.</td>
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<td>2016</td>
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<td>Scientific reports</td>
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||
<td><a target="_blank" href="/pubmed/27574448"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">27574448</a>
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</td>
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||
<td class="fir_col">Polymorphism of CYP3A4 and ABCB1 genes increase the risk of neuropathy in breast cancer patients treated with paclitaxel and docetaxel.</td>
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<td>Kus T et al.</td>
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<td>2016</td>
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<td>OncoTargets and therapy</td>
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||
<td><a target="_blank" href="/pubmed/27588484"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27588484</a>
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<td class="fir_col">Gene-gene interactions in gastrointestinal cancer susceptibility.</td>
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<td>Kim J et al.</td>
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<td>2016</td>
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<td>Oncotarget</td>
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<td><a target="_blank" href="/pubmed/27614750"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27614750</a>
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</td>
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<td class="fir_col">Association of p53 codon 72 polymorphism and survival of North Indian lung cancer patients treated with platinum-based chemotherapy.</td>
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<td>Kumari A et al.</td>
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<td>2016</td>
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<td>Molecular biology reports</td>
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<td><a target="_blank" href="/pubmed/27618021"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">27618021</a>
|
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</td>
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<td class="fir_col">Pharmacogenomics in Pediatric Oncology: Review of Gene-Drug Associations for Clinical Use.</td>
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<td>Mlakar V et al.</td>
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<td>2016</td>
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<td>International journal of molecular sciences</td>
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||
<td><a target="_blank" href="/pubmed/27619989"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27619989</a>
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</td>
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||
<td class="fir_col">Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia cases.</td>
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<td>Hamadou WS et al.</td>
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<td>2017</td>
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<td>Familial cancer</td>
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||
<td><a target="_blank" href="/pubmed/27658049"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27658049</a>
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<td class="fir_col">Molecular Genetic Characterization of Individual Cancer Cells Isolated via Single-Cell Printing.</td>
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<td>Riba J et al.</td>
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<td>2016</td>
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<td>PloS one</td>
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<td><a target="_blank" href="/pubmed/27686769"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27686769</a>
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<td class="fir_col">[Association and interaction of heat shock proteins B1 gene and tumor-suppressor protein p53 gene with chromosome damage levels among coke oven workers].</td>
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<td>Li XL et al.</td>
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<td>2016</td>
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<td>Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]</td>
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<td><a target="_blank" href="/pubmed/27698805"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27698805</a>
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</td>
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<td class="fir_col">Genetic landscape of a case of extraovarian peritoneal serous papillary carcinoma.</td>
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<td>Cheng Z et al.</td>
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<td>2016</td>
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<td>Oncology letters</td>
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||
<td><a target="_blank" href="/pubmed/27716216"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27716216</a>
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</td>
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<td class="fir_col">The Anatomy to Genomics (ATG) Start Genetics medical school initiative: incorporating exome sequencing data from cadavers used for Anatomy instruction into the first year curriculum.</td>
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<td>Gerhard GS et al.</td>
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<td>2016</td>
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<td>BMC medical genomics</td>
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<td><a target="_blank" href="/pubmed/27852141"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27852141</a>
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</td>
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<td class="fir_col">A polymorphism (rs1042522) in TP53 gene is a risk factor for Down Syndrome in Sicilian mothers.</td>
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<td>Salemi M et al.</td>
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<td>2017</td>
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<td>The journal of maternal-fetal & neonatal medicine </td>
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<td><a target="_blank" href="/pubmed/27871254"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">27871254</a>
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<td class="fir_col">Familial aggregation of albuminuria and arterial hypertension in an Aboriginal Australian community and the contribution of variants in ACE and TP53.</td>
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<td>Duffy DL et al.</td>
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<td>2016</td>
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||
<td>BMC nephrology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/27900359"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27900359</a>
|
||
</td>
|
||
<td class="fir_col">Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs.</td>
|
||
<td>Kukita Y et al.</td>
|
||
<td>2016</td>
|
||
<td>Cold Spring Harbor molecular case studies</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28106707"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28106707</a>
|
||
</td>
|
||
<td class="fir_col">ASSOCIATION STUDY BETWEEN POLYMORPHISMS OF THE p53 AND LYMPHOTOXIN ALPHA (LTA) GENES AND THE RISK OF PROLIFERATIVE VITREORETINOPATHY/RETINAL DETACHMENT IN A MEXICAN POPULATION.</td>
|
||
<td>Quiroz-Casian N et al.</td>
|
||
<td>2018</td>
|
||
<td>Retina (Philadelphia, Pa.)</td>
|
||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28125715"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28125715</a>
|
||
</td>
|
||
<td class="fir_col">Correction: Study of Association between Pre-Senile Cataracts and the Polymorphisms rs2228000 in XPC and rs1042522 in p53 in Spanish Population.</td>
|
||
<td>López Valverde G et al.</td>
|
||
<td>2017</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28179045"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28179045</a>
|
||
</td>
|
||
<td class="fir_col">Analysis of Polymorphism rs1042522 in TP53 Gene in the Mothers of Twins and of Singletons: A Population-Based Study in Rio Grande do Sul, Brazil.</td>
|
||
<td>Mardini AC et al.</td>
|
||
<td>2017</td>
|
||
<td>Twin research and human genetics </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28184992"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28184992</a>
|
||
</td>
|
||
<td class="fir_col">Association study between the TP53 Rs1042522G/C polymorphism and susceptibility to systemic lupus erythematosus in a Chinese Han population.</td>
|
||
<td>Yang J et al.</td>
|
||
<td>2017</td>
|
||
<td>Rheumatology international</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28210099"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28210099</a>
|
||
</td>
|
||
<td class="fir_col">Study of polymorphisms in the TP53 and RB1 genes in children with retinoblastoma in northern Mexico.</td>
|
||
<td>Anaya-Pava EJ et al.</td>
|
||
<td>2017</td>
|
||
<td>Molecular vision</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28214592"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28214592</a>
|
||
</td>
|
||
<td class="fir_col">Role of a p53 polymorphism in the development of nonfunctional pituitary adenomas.</td>
|
||
<td>Yagnik G et al.</td>
|
||
<td>2017</td>
|
||
<td>Molecular and cellular endocrinology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28260929"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28260929</a>
|
||
</td>
|
||
<td class="fir_col">Association between TP53 gene Arg72Pro polymorphism and Wilms' tumor risk in a Chinese population.</td>
|
||
<td>Fu W et al.</td>
|
||
<td>2017</td>
|
||
<td>OncoTargets and therapy</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28275206"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28275206</a>
|
||
</td>
|
||
<td class="fir_col">The TP53 gene rs1042522 C>G polymorphism and neuroblastoma risk in Chinese children.</td>
|
||
<td>He J et al.</td>
|
||
<td>2017</td>
|
||
<td>Aging</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28336930"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28336930</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals.</td>
|
||
<td>Kodal JB et al.</td>
|
||
<td>2017</td>
|
||
<td>Scientific reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28348449"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28348449</a>
|
||
</td>
|
||
<td class="fir_col">Combined Genetic Biomarkers Confer Susceptibility to Risk of Urothelial Bladder Carcinoma in a Saudi Population.</td>
|
||
<td>Elhawary NA et al.</td>
|
||
<td>2017</td>
|
||
<td>Disease markers</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28351583"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28351583</a>
|
||
</td>
|
||
<td class="fir_col">Candidate apoptotic and DNA repair gene approach confirms involvement of ERCC1, ERCC5, TP53 and MDM2 in radiation-induced toxicity in head and neck cancer.</td>
|
||
<td>Borchiellini D et al.</td>
|
||
<td>2017</td>
|
||
<td>Oral oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28364582"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28364582</a>
|
||
</td>
|
||
<td class="fir_col">Clinical relevance of TP53 polymorphic genetic variations in chronic lymphocytic leukemia.</td>
|
||
<td>Bilous N et al.</td>
|
||
<td>2017</td>
|
||
<td>Leukemia research</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28373458"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28373458</a>
|
||
</td>
|
||
<td class="fir_col">Low Variability and Stable Frequency of Common Haplotypes of the TP53 Gene Region in Colorectal Cancer Patients in a Slovak Population.</td>
|
||
<td>Škereňová M et al.</td>
|
||
<td>2017</td>
|
||
<td>Anticancer research</td>
|
||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28415781"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28415781</a>
|
||
</td>
|
||
<td class="fir_col">Relevance of DNA repair gene polymorphisms to gastric cancer risk and phenotype.</td>
|
||
<td>Carrera-Lasfuentes P et al.</td>
|
||
<td>2017</td>
|
||
<td>Oncotarget</td>
|
||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28456797"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28456797</a>
|
||
</td>
|
||
<td class="fir_col">Identification of Two Additional Susceptibility Loci for Inflammatory Bowel Disease in a Chinese Population.</td>
|
||
<td>Lan X et al.</td>
|
||
<td>2017</td>
|
||
<td>Cellular physiology and biochemistry </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28545270"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28545270</a>
|
||
</td>
|
||
<td class="fir_col">[Correlation between mutation of p53 gene 2-4 exons from peripheral blood and HPV16 positive cervical cancer susceptibility and clinical significance].</td>
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||
<td>Yin CM et al.</td>
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||
<td>2017</td>
|
||
<td>Zhonghua fu chan ke za zhi</td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28652652"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28652652</a>
|
||
</td>
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||
<td class="fir_col">Gallbladder cancer epidemiology, pathogenesis and molecular genetics: Recent update.</td>
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||
<td>Sharma A et al.</td>
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||
<td>2017</td>
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||
<td>World journal of gastroenterology</td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28827732"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28827732</a>
|
||
</td>
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||
<td class="fir_col">Genetic predisposition to lung cancer: comprehensive literature integration, meta-analysis, and multiple evidence assessment of candidate-gene association studies.</td>
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||
<td>Wang J et al.</td>
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||
<td>2017</td>
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<td>Scientific reports</td>
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</tr>
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||
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28866361"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28866361</a>
|
||
</td>
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||
<td class="fir_col">Targeted next-generation sequencing of glandular odontogenic cyst: a preliminary study.</td>
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||
<td>Siqueira EC et al.</td>
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||
<td>2017</td>
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||
<td>Oral surgery, oral medicine, oral pathology and oral radiology</td>
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||
</tr>
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||
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28881764"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28881764</a>
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||
</td>
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||
<td class="fir_col">Detection of nasopharyngeal carcinoma susceptibility with single nucleotide polymorphism analysis using next-generation sequencing technology.</td>
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||
<td>Wu MY et al.</td>
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||
<td>2017</td>
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||
<td>Oncotarget</td>
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||
</tr>
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||
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29063062"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29063062</a>
|
||
</td>
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||
<td class="fir_col">Association between the rs1042522 polymorphism in TP53 and prostate cancer risk: An updated meta-analysis.</td>
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||
<td>Fan S et al.</td>
|
||
<td>2017</td>
|
||
<td>Chronic diseases and translational medicine</td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29126407"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29126407</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Arg72 as a favorable prognostic factor for Chinese diffuse large B-cell lymphoma patients treated with CHOP.</td>
|
||
<td>Liu Y et al.</td>
|
||
<td>2017</td>
|
||
<td>BMC cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29167767"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29167767</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Gene Polymorphisms and Occupational Skin Cancer Risks for Workers of Glass Fiber Manufacture.</td>
|
||
<td>Mukhammadiyeva GF et al.</td>
|
||
<td>2017</td>
|
||
<td>Iranian journal of public health</td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29193749"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29193749</a>
|
||
</td>
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||
<td class="fir_col">Clinical Implementation of Pharmacogenetic Testing in a Hospital of the Spanish National Health System: Strategy and Experience Over 3 Years.</td>
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||
<td>Borobia AM et al.</td>
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||
<td>2018</td>
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||
<td>Clinical and translational science</td>
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</tr>
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||
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29239811"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29239811</a>
|
||
</td>
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||
<td class="fir_col">The Wnt/β-catenin pathway is deregulated in cemento-ossifying fibromas.</td>
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||
<td>Pereira TDSF et al.</td>
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||
<td>2018</td>
|
||
<td>Oral surgery, oral medicine, oral pathology and oral radiology</td>
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</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29286614"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29286614</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Gene Pro72Arg (rs1042522) Single Nucleotide Polymorphism as Not a Risk Factor for Colorectal Cancer in the Iranian Azari Population.</td>
|
||
<td>Asadi M et al.</td>
|
||
<td>2017</td>
|
||
<td>Asian Pacific journal of cancer prevention </td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29356585"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29356585</a>
|
||
</td>
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||
<td class="fir_col">Correlation Between Single-Nucleotide Polymorphisms Within miR-30a and Related Target Genes and Risk or Prognosis of Nephrotic Syndrome.</td>
|
||
<td>Yang R et al.</td>
|
||
<td>2018</td>
|
||
<td>DNA and cell biology</td>
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||
</tr>
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||
|
||
<tr>
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||
<td><a target="_blank" href="/pubmed/29390357"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29390357</a>
|
||
</td>
|
||
<td class="fir_col">Association between rs11200014, rs2981579, and rs1219648 polymorphism and breast cancer susceptibility: A meta-analysis.</td>
|
||
<td>Zhang Y et al.</td>
|
||
<td>2017</td>
|
||
<td>Medicine</td>
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||
</tr>
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||
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||
<tr>
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||
<td><a target="_blank" href="/pubmed/29458332"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29458332</a>
|
||
</td>
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||
<td class="fir_col">Identification of genetic variants for clinical management of familial colorectal tumors.</td>
|
||
<td>Dominguez-Valentin M et al.</td>
|
||
<td>2018</td>
|
||
<td>BMC medical genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29482350"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29482350</a>
|
||
</td>
|
||
<td class="fir_col">Tumor Protein p53 (TP53) Gene and Left Main Coronary Artery Disease.</td>
|
||
<td>Kolovou V et al.</td>
|
||
<td>2018</td>
|
||
<td>Angiology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29484706"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29484706</a>
|
||
</td>
|
||
<td class="fir_col">Identification of a novel truncating mutation in PALB2 gene by a multigene sequencing panel for mutational screening of breast cancer risk-associated and related genes.</td>
|
||
<td>Guacci A et al.</td>
|
||
<td>2018</td>
|
||
<td>Journal of clinical laboratory analysis</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29658252"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29658252</a>
|
||
</td>
|
||
<td class="fir_col">[Single nucleotide polymorphism of the TP53 gene is not correlated with male infertility].</td>
|
||
<td>Ni MX et al.</td>
|
||
<td>2017</td>
|
||
<td>Zhonghua nan ke xue = National journal of andrology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29731921"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29731921</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Arg72Pro polymorphism is associated with increased overall survival but not response to therapy in Portuguese/Caucasian patients with advanced cervical cancer.</td>
|
||
<td>Coelho A et al.</td>
|
||
<td>2018</td>
|
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<td>Oncology letters</td>
|
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</tr>
|
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|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29860059"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29860059</a>
|
||
</td>
|
||
<td class="fir_col">Influence of tumour suppressor gene (TP53, BRCA1 and BRCA2) polymorphisms on polycystic ovary syndrome in South Indian women.</td>
|
||
<td>Siddamalla S et al.</td>
|
||
<td>2018</td>
|
||
<td>European journal of obstetrics, gynecology, and reproductive biology</td>
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</tr>
|
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||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29949804"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29949804</a>
|
||
</td>
|
||
<td class="fir_col">The 72Pro Variant of the Tumor Protein 53 Is Associated with an Increased Breast Cancer Risk in the Moroccan Population.</td>
|
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<td>Ayoubi SE et al.</td>
|
||
<td>2018</td>
|
||
<td>Pathobiology </td>
|
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/29957069"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29957069</a>
|
||
</td>
|
||
<td class="fir_col">Associations Between TP53 and MDM2 Polymorphisms and the Follicle-Stimulating Hormone/Luteinizing Hormone Ratio in Infertile Women.</td>
|
||
<td>Chan Y et al.</td>
|
||
<td>2018</td>
|
||
<td>Genetic testing and molecular biomarkers</td>
|
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</tr>
|
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|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/30126398"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30126398</a>
|
||
</td>
|
||
<td class="fir_col">Effect of TP53 rs1042522 on the susceptibility of patients to oral squamous cell carcinoma and oral leukoplakia: a meta-analysis.</td>
|
||
<td>Sun Z et al.</td>
|
||
<td>2018</td>
|
||
<td>BMC oral health</td>
|
||
</tr>
|
||
|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/30139066"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30139066</a>
|
||
</td>
|
||
<td class="fir_col">Meta-Analysis of Polymorphic Variants Conferring Genetic Risk to Cervical Cancer in Indian Women Supports CYP1A1 as an Important Associated Locus.</td>
|
||
<td>Sengupta D et al.</td>
|
||
<td>2018</td>
|
||
<td>Asian Pacific journal of cancer prevention </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30235774"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30235774</a>
|
||
</td>
|
||
<td class="fir_col">Systematic meta-analysis of genetic variants associated with osteosarcoma susceptibility.</td>
|
||
<td>Wang X et al.</td>
|
||
<td>2018</td>
|
||
<td>Medicine</td>
|
||
</tr>
|
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|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30288482"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30288482</a>
|
||
</td>
|
||
<td class="fir_col">The frequency of TP53 R72P and MDM2 309T>G polymorphisms in Iranian infertile men with spermatogenetic failure: A case-control study.</td>
|
||
<td>Ebrahim Abadi Z et al.</td>
|
||
<td>2018</td>
|
||
<td>International journal of reproductive biomedicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30337837"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30337837</a>
|
||
</td>
|
||
<td class="fir_col">Single nucleotide polymorphisms and sporadic colorectal cancer susceptibility: a field synopsis and meta-analysis.</td>
|
||
<td>Wen J et al.</td>
|
||
<td>2018</td>
|
||
<td>Cancer cell international</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30370260"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30370260</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphism Located in the Upstream Region of the RPS19 Gene (rs2305809) Is Associated With Cervical Cancer: A Case-control Study.</td>
|
||
<td>da Rocha Boeira T et al.</td>
|
||
<td>2018</td>
|
||
<td>Journal of cancer prevention</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30409984"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30409984</a>
|
||
</td>
|
||
<td class="fir_col">Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics.</td>
|
||
<td>John SE et al.</td>
|
||
<td>2018</td>
|
||
<td>Scientific reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30519324"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30519324</a>
|
||
</td>
|
||
<td class="fir_col">P53 Codon 72 Polymorphism and Risk for Squamous Cell Carcinoma of the Penis: A Caucasian Case-Control Study.</td>
|
||
<td>Stoehr R et al.</td>
|
||
<td>2018</td>
|
||
<td>Journal of Cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30551681"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30551681</a>
|
||
</td>
|
||
<td class="fir_col">Association between Polymorphisms in Inflammatory Response-Related Genes and the Susceptibility, Progression and Prognosis of the Diffuse Histological Subtype of Gastric Cancer.</td>
|
||
<td>Furuya TK et al.</td>
|
||
<td>2018</td>
|
||
<td>Genes</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30607176"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30607176</a>
|
||
</td>
|
||
<td class="fir_col">Association of rs1042522 SNP with Clinicopathologic Factors of Breast Cancer Patients in the Markazi Province of Iran.</td>
|
||
<td>Anoushirvani AA et al.</td>
|
||
<td>2018</td>
|
||
<td>Open access Macedonian journal of medical sciences</td>
|
||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30610160"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30610160</a>
|
||
</td>
|
||
<td class="fir_col">TP53 rs1042522 C>G polymorphism and Wilms tumor susceptibility in Chinese children: a four-center case-control study.</td>
|
||
<td>Liu P et al.</td>
|
||
<td>2019</td>
|
||
<td>Bioscience reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30616520"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30616520</a>
|
||
</td>
|
||
<td class="fir_col">Interaction between TP53 and XRCC1 increases susceptibility to cervical cancer development: a case control study.</td>
|
||
<td>Liu GC et al.</td>
|
||
<td>2019</td>
|
||
<td>BMC cancer</td>
|
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</tr>
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|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30686012"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">30686012</a>
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</td>
|
||
<td class="fir_col">TP53 rs1042522 and rs8064946 variants in myocardial infarction.</td>
|
||
<td>Hakobjanyan A et al.</td>
|
||
<td>2018</td>
|
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<td>Bratislavske lekarske listy</td>
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|
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<tr>
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<td><a target="_blank" href="/pubmed/30695351"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30695351</a>
|
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</td>
|
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<td class="fir_col">[ASSOCIATION OF CERTAIN SINGLE NUCLEOTIDE POLYMORPHISM GENES OF APOPTOSIS SYSTEM WITH A RISK OF DEVELOPMENT OF COLORECTAL CANCER IN RUSSIAN POPULATION].</td>
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<td>Alyeva MK et al.</td>
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<td>2016</td>
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<td>Zhurnal mikrobiologii, epidemiologii i immunobiologii</td>
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<tr>
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<td><a target="_blank" href="/pubmed/30719141"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30719141</a>
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</td>
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<td class="fir_col">TP53 gene rs1042522 allele G decreases neuroblastoma risk: a two-centre case-control study.</td>
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<td>Zhang J et al.</td>
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<td>2019</td>
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<td>Journal of Cancer</td>
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<tr>
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||
<td><a target="_blank" href="/pubmed/30781715"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30781715</a>
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</td>
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<td class="fir_col">Genetic Epidemiology of Breast Cancer in Latin America.</td>
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<td>Zavala VA et al.</td>
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<td>2019</td>
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<td>Genes</td>
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<td><a target="_blank" href="/pubmed/30793520"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30793520</a>
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</td>
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<td class="fir_col">Cumulative evidence for association between genetic polymorphisms and esophageal cancer susceptibility: A review with evidence from meta-analysis and genome-wide association studies.</td>
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<td>Tian J et al.</td>
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<td>2019</td>
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<td>Cancer medicine</td>
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<tr>
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||
<td><a target="_blank" href="/pubmed/30796655"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30796655</a>
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</td>
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<td class="fir_col">Germline TP53 mutation spectrum in Sudanese premenopausal breast cancer patients: correlations with reproductive factors.</td>
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<td>Aceto GM et al.</td>
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||
<td>2019</td>
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<td>Breast cancer research and treatment</td>
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<tr>
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||
<td><a target="_blank" href="/pubmed/30799775"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30799775</a>
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</td>
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<td class="fir_col">Association of Single-Nucleotide Polymorphisms in Monoubiquitinated FANCD2-DNA Damage Repair Pathway Genes With Breast Cancer in the Chinese Population.</td>
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<td>Chen FY et al.</td>
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<td>2018</td>
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<td>Technology in cancer research & treatment</td>
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<td><a target="_blank" href="/pubmed/30807515"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30807515</a>
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</td>
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<td class="fir_col">SINGLE NUCLEOTIDE POLYMORPHISMS IN RETINAL DETACHMENT PATIENTS WITH AND WITHOUT PROLIFERATIVE VITREORETINOPATHY.</td>
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<td>Lumi X et al.</td>
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<td>2020</td>
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<td>Retina (Philadelphia, Pa.)</td>
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<tr>
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||
<td><a target="_blank" href="/pubmed/30833364"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30833364</a>
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</td>
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<td class="fir_col">Association between TP53 rs1042522 gene polymorphism and the risk of malignant bone tumors: a meta-analysis.</td>
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<td>Huang X et al.</td>
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<td>2019</td>
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<td>Bioscience reports</td>
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<tr>
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<td><a target="_blank" href="/pubmed/30841568"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30841568</a>
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</td>
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||
<td class="fir_col">Intake of Red and Processed Meat, Use of Non-Steroid Anti-Inflammatory Drugs, Genetic Variants and Risk of Colorectal Cancer: A Prospective Study of the Danish "Diet, Cancer and Health" Cohort.</td>
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||
<td>Andersen V et al.</td>
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<td>2019</td>
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<td>International journal of molecular sciences</td>
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<td><a target="_blank" href="/pubmed/30867801"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30867801</a>
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<td class="fir_col">Genetic alterations of triple negative breast cancer (TNBC) in women from Northeastern Mexico.</td>
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<td>Uscanga-Perales GI et al.</td>
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<td>2019</td>
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<td>Oncology letters</td>
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<td><a target="_blank" href="/pubmed/30956778"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30956778</a>
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</td>
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<td class="fir_col">Specific allelic variants of SNPs in the MDM2 and MDMX genes are associated with earlier tumor onset and progression in Caucasian breast cancer patients.</td>
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<td>Bauer M et al.</td>
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<td>2019</td>
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<td>Oncotarget</td>
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<tr>
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<td><a target="_blank" href="/pubmed/30959967"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30959967</a>
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</td>
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<td class="fir_col">Genetic Susceptibility in Head and Neck Squamous Cell Carcinoma in a Spanish Population.</td>
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<td>Fernández-Mateos J et al.</td>
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<td>Cancers</td>
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<td><a target="_blank" href="/pubmed/30972159"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30972159</a>
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</td>
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<td class="fir_col">Mechanistic insights into environmental and genetic risk factors for systemic lupus erythematosus.</td>
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<td>Pan Q et al.</td>
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<td>2019</td>
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<td>American journal of translational research</td>
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<td><a target="_blank" href="/pubmed/30988702"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">30988702</a>
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</td>
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<td class="fir_col">Defining the genetic profile of endometriosis.</td>
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<td>Vassilopoulou L et al.</td>
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<td>2019</td>
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<td>Experimental and therapeutic medicine</td>
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<td><a target="_blank" href="/pubmed/31028217"
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||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">31028217</a>
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</td>
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<td class="fir_col">Impact of MDM2, TP53 and P14ARF Polymorphisms on Endometrial Cancer Risk and Onset.</td>
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<td>Wujcicka W et al.</td>
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<td>2019</td>
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<td>In vivo (Athens, Greece)</td>
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<td><a target="_blank" href="/pubmed/31055723"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">31055723</a>
|
||
</td>
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<td class="fir_col">TP53 Polymorphism Contributes to the Susceptibility to Bipolar Disorder but Not to Schizophrenia in the Chinese Han Population.</td>
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<td>Yang J et al.</td>
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<td>2019</td>
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<td>Journal of molecular neuroscience </td>
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">31123171</a>
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</td>
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<td class="fir_col">Association of miR-146a, miR-149 and miR-196a2 polymorphisms with neuroblastoma risk in Eastern Chinese population: a three-center case-control study.</td>
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<td>Zhou C et al.</td>
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<td>2019</td>
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<td>Bioscience reports</td>
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<tr>
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||
<td><a target="_blank" href="/pubmed/31128065"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31128065</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Gene 72 Arg/Pro (rs1042522) Single Nucleotide Polymorphism Contribute to Increase the Risk of B-Chronic Lymphocytic Leukemia in the Sudanese Population.</td>
|
||
<td>Mohammed Basabaeen AA et al.</td>
|
||
<td>2019</td>
|
||
<td>Asian Pacific journal of cancer prevention </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31205533"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31205533</a>
|
||
</td>
|
||
<td class="fir_col">Five P53 SNPs Involved in Low Rectal Cancer Risk and Prognosis in a Chinese Population.</td>
|
||
<td>Zhang G et al.</td>
|
||
<td>2019</td>
|
||
<td>Journal of Cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31211452"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31211452</a>
|
||
</td>
|
||
<td class="fir_col">Long telomeres cooperate with p53, MDM2, and p21 polymorphisms to raise pediatric solid tumor risk.</td>
|
||
<td>Borbora D et al.</td>
|
||
<td>2019</td>
|
||
<td>Pediatrics international </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31293648"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31293648</a>
|
||
</td>
|
||
<td class="fir_col">Association of the TP53 rs1042522 C>G polymorphism and hepatoblastoma risk in Chinese children.</td>
|
||
<td>Yang T et al.</td>
|
||
<td>2019</td>
|
||
<td>Journal of Cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31325764"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31325764</a>
|
||
</td>
|
||
<td class="fir_col">Association of miR-34b/c rs4938723 and TP53 Arg72Pro Polymorphisms with Neuroblastoma Susceptibility: Evidence from Seven Centers.</td>
|
||
<td>Li L et al.</td>
|
||
<td>2019</td>
|
||
<td>Translational oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31387111"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31387111</a>
|
||
</td>
|
||
<td class="fir_col">Haplotype and linkage disequilibrium of TP53-WRAP53 locus in Iranian-Azeri women with breast cancer.</td>
|
||
<td>Pouladi N et al.</td>
|
||
<td>2019</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31435875"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31435875</a>
|
||
</td>
|
||
<td class="fir_col">Inherited alterations of TGF beta signaling components in Appalachian cervical cancers.</td>
|
||
<td>Knobloch TJ et al.</td>
|
||
<td>2019</td>
|
||
<td>Cancer causes & control </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31441737"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31441737</a>
|
||
</td>
|
||
<td class="fir_col">[Prognostic role of p53 gene polymorphism in risk assessment of anthracycline-induced cardiotoxicity].</td>
|
||
<td>Shilov SN et al.</td>
|
||
<td>2019</td>
|
||
<td>Kardiologiia</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31528229"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31528229</a>
|
||
</td>
|
||
<td class="fir_col">Correlation between Candidate Single Nucleotide Variants and Several Clinicopathological Risk Factors Related to Breast Cancer in Jordanian Women: A Genotype-Phenotype Study.</td>
|
||
<td>Al-Eitan LN et al.</td>
|
||
<td>2019</td>
|
||
<td>Journal of Cancer</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31612033"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31612033</a>
|
||
</td>
|
||
<td class="fir_col">The complementary effect of rs1042522 in TP53 and rs1805007 in MC1R is associated with an elevated risk of cutaneous melanoma in Latvian population.</td>
|
||
<td>Ozola A et al.</td>
|
||
<td>2019</td>
|
||
<td>Oncology letters</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31703578"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31703578</a>
|
||
</td>
|
||
<td class="fir_col">Analysis of polymorphisms, promoter methylation, and mRNA expression profile of maternal and placental P53 and P21 genes in preeclamptic and normotensive pregnant women.</td>
|
||
<td>Harati-Sadegh M et al.</td>
|
||
<td>2019</td>
|
||
<td>Journal of biomedical science</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31721533"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31721533</a>
|
||
</td>
|
||
<td class="fir_col">The Dilemma of TP53 Codon 72 Polymorphism (rs1042522) and Breast Cancer Risk: A Case-Control Study and Meta-Analysis in The Iranian Population.</td>
|
||
<td>Afzaljavan F et al.</td>
|
||
<td>2020</td>
|
||
<td>Cell journal</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31762593"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31762593</a>
|
||
</td>
|
||
<td class="fir_col">The genetic association study of TP53 polymorphisms in Saudi obese patients.</td>
|
||
<td>Sabir JSM et al.</td>
|
||
<td>2019</td>
|
||
<td>Saudi journal of biological sciences</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31788124"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31788124</a>
|
||
</td>
|
||
<td class="fir_col">p53 protein expression affected by TP53 polymorphism is associated with the biological behavior and prognosis of low rectal cancer.</td>
|
||
<td>Zhang G et al.</td>
|
||
<td>2019</td>
|
||
<td>Oncology letters</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31818908"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31818908</a>
|
||
</td>
|
||
<td class="fir_col">Systematic meta-analyses, field synopsis and global assessment of the evidence of genetic association studies in colorectal cancer.</td>
|
||
<td>Montazeri Z et al.</td>
|
||
<td>2020</td>
|
||
<td>Gut</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31821471"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31821471</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms and endometriosis: a systematic review and meta-analyses.</td>
|
||
<td>Méar L et al.</td>
|
||
<td>2020</td>
|
||
<td>Human reproduction update</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31827503"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31827503</a>
|
||
</td>
|
||
<td class="fir_col">Two Functional TP53 Genetic Variants and Predisposition to Keloid Scarring in Caucasians.</td>
|
||
<td>Dmytrzak A et al.</td>
|
||
<td>2019</td>
|
||
<td>Dermatology research and practice</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31870105"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31870105</a>
|
||
</td>
|
||
<td class="fir_col">Carcinogen Metabolism Pathway and Tumor Suppressor Gene Polymorphisms and Gallbladder Cancer Risk in North Indians: A Hospital-Based Case-Control Study.</td>
|
||
<td>Asai T et al.</td>
|
||
<td>2019</td>
|
||
<td>Asian Pacific journal of cancer prevention </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31895498"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31895498</a>
|
||
</td>
|
||
<td class="fir_col">The effect of TP53 and P21 gene polymorphisms on papillary thyroid carcinoma susceptibility and clinical/pathological features.</td>
|
||
<td>Heidari Z et al.</td>
|
||
<td>2020</td>
|
||
<td>IUBMB life</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31909567"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31909567</a>
|
||
</td>
|
||
<td class="fir_col">Interactions among variants in P53 apoptotic pathway genes are associated with neurologic deterioration and functional outcome after acute ischemic stroke.</td>
|
||
<td>Yi X et al.</td>
|
||
<td>2021</td>
|
||
<td>Brain and behavior</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32001373"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32001373</a>
|
||
</td>
|
||
<td class="fir_col">Genetic polymorphisms of TP53 (rs1042522) and MDM2 (rs2279744) and colorectal cancer risk: An updated meta-analysis based on 59 case-control studies.</td>
|
||
<td>Elshazli RM et al.</td>
|
||
<td>2020</td>
|
||
<td>Gene</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32080966"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32080966</a>
|
||
</td>
|
||
<td class="fir_col">Effect of maternal HIV infection, BMI and NOx air pollution exposure on birth outcomes in South African pregnant women genotyped for the p53 Pro72Arg (rs1042522).</td>
|
||
<td>Naidoo P et al.</td>
|
||
<td>2020</td>
|
||
<td>International journal of immunogenetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32083300"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32083300</a>
|
||
</td>
|
||
<td class="fir_col">The association of miR34b/c and TP53 gene polymorphisms with Wilms tumor risk in Chinese children.</td>
|
||
<td>Wang J et al.</td>
|
||
<td>2020</td>
|
||
<td>Bioscience reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32166848"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32166848</a>
|
||
</td>
|
||
<td class="fir_col">Association of TP53 rs1042522 C>G and miR-34b/c rs4938723 T>C polymorphisms with hepatoblastoma susceptibility: A seven-center case-control study.</td>
|
||
<td>Liu P et al.</td>
|
||
<td>2020</td>
|
||
<td>The journal of gene medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32207313"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32207313</a>
|
||
</td>
|
||
<td class="fir_col">Genetic Variation in the TP53 Gene and Patient Outcomes Following Severe Traumatic Brain Injury.</td>
|
||
<td>Mellett K et al.</td>
|
||
<td>2020</td>
|
||
<td>Biological research for nursing</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32233050"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32233050</a>
|
||
</td>
|
||
<td class="fir_col">Association of TP53 rs1042522 with cervical cancer in the sub-Saharan African population: a meta-analysis.</td>
|
||
<td>Kamiza AB et al.</td>
|
||
<td>2020</td>
|
||
<td>Tropical medicine & international health </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32287273"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32287273</a>
|
||
</td>
|
||
<td class="fir_col">DOT: Gene-set analysis by combining decorrelated association statistics.</td>
|
||
<td>Vsevolozhskaya OA et al.</td>
|
||
<td>2020</td>
|
||
<td>PLoS computational biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32338278"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32338278</a>
|
||
</td>
|
||
<td class="fir_col">Genetic polymorphisms as non-modifiable susceptibility factors to laryngeal cancer.</td>
|
||
<td>Escalante P et al.</td>
|
||
<td>2020</td>
|
||
<td>Bioscience reports</td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32406493"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32406493</a>
|
||
</td>
|
||
<td class="fir_col">TP53 Arg72Pro polymorphism and neuroblastoma susceptibility in eastern Chinese children: a three-center case-control study.</td>
|
||
<td>Fang Y et al.</td>
|
||
<td>2020</td>
|
||
<td>Bioscience reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32419782"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32419782</a>
|
||
</td>
|
||
<td class="fir_col">TP53 rs1042522 polymorphism and early-onset breast cancer.</td>
|
||
<td>Icen-Taskin I et al.</td>
|
||
<td>2020</td>
|
||
<td>Journal of research in medical sciences </td>
|
||
</tr>
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|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32492903"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32492903</a>
|
||
</td>
|
||
<td class="fir_col">Association Analysis of TP53 rs1042522, MDM2 rs2279744, rs3730485, MDM4 rs4245739 Variants and Acute Myeloid Leukemia Susceptibility, Risk Stratification Scores, and Clinical Features: An Exploratory Study.</td>
|
||
<td>Tripon F et al.</td>
|
||
<td>2020</td>
|
||
<td>Journal of clinical medicine</td>
|
||
</tr>
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|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/32550823"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32550823</a>
|
||
</td>
|
||
<td class="fir_col">Application of targeted next generation sequencing for the mutational profiling of patients with acute lymphoblastic leukemia.</td>
|
||
<td>Janic D et al.</td>
|
||
<td>2020</td>
|
||
<td>Journal of medical biochemistry</td>
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</tr>
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<tr>
|
||
<td><a target="_blank" href="/pubmed/32651972"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32651972</a>
|
||
</td>
|
||
<td class="fir_col">Association of polymorphisms in TP53 and the promoter region of IL10 with gastric cancer in a Kazakh population.</td>
|
||
<td>Kulmambetova G et al.</td>
|
||
<td>2020</td>
|
||
<td>Bosnian journal of basic medical sciences</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32655615"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32655615</a>
|
||
</td>
|
||
<td class="fir_col">Novel Genetic Variations in Acute Myeloid Leukemia in Pakistani Population.</td>
|
||
<td>Shahid S et al.</td>
|
||
<td>2020</td>
|
||
<td>Frontiers in genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32821748"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32821748</a>
|
||
</td>
|
||
<td class="fir_col">Evaluation of TP53 Codon 72, P21 Codon 31, and MDM2 SNP309 Polymorphisms in Iranian Patients with Acute Lymphocytic Leukemia.</td>
|
||
<td>Lotfi Garavand A et al.</td>
|
||
<td>2020</td>
|
||
<td>Reports of biochemistry & molecular biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32882831"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32882831</a>
|
||
</td>
|
||
<td class="fir_col">Intronic TP53 Polymorphisms Are Associated with Increased Δ133TP53 Transcript, Immune Infiltration and Cancer Risk.</td>
|
||
<td>Eiholzer RA et al.</td>
|
||
<td>2020</td>
|
||
<td>Cancers</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32888145"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32888145</a>
|
||
</td>
|
||
<td class="fir_col">Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population.</td>
|
||
<td>Rogoża-Janiszewska E et al.</td>
|
||
<td>2021</td>
|
||
<td>Breast cancer (Tokyo, Japan)</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32972771"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32972771</a>
|
||
</td>
|
||
<td class="fir_col">Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia.</td>
|
||
<td>Rosas I et al.</td>
|
||
<td>2021</td>
|
||
<td>Neurobiology of aging</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33126568"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33126568</a>
|
||
</td>
|
||
<td class="fir_col">The P72R Polymorphism in R248Q/W p53 Mutants Modifies the Mutant Effect on Epithelial to Mesenchymal Transition Phenotype and Cell Invasion via CXCL1 Expression.</td>
|
||
<td>De Souza C et al.</td>
|
||
<td>2020</td>
|
||
<td>International journal of molecular sciences</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33257846"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33257846</a>
|
||
</td>
|
||
<td class="fir_col">Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene.</td>
|
||
<td>Doffe F et al.</td>
|
||
<td>2021</td>
|
||
<td>Cell death and differentiation</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33262486"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33262486</a>
|
||
</td>
|
||
<td class="fir_col">Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters.</td>
|
||
<td></td>
|
||
<td>2020</td>
|
||
<td>European journal of human genetics </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33290139"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33290139</a>
|
||
</td>
|
||
<td class="fir_col">A Shared Susceptibility Locus in the p53 Gene for both Gastric and Esophageal Cancers in a Northwestern Chinese Population.</td>
|
||
<td>Cao J et al.</td>
|
||
<td>2020</td>
|
||
<td>Genetic testing and molecular biomarkers</td>
|
||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33297469"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33297469</a>
|
||
</td>
|
||
<td class="fir_col">Current and New Biomarkers for Early Detection, Prognostic Stratification, and Management of Gallbladder Cancer Patients.</td>
|
||
<td>García P et al.</td>
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||
<td>2020</td>
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||
<td>Cancers</td>
|
||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33481818"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33481818</a>
|
||
</td>
|
||
<td class="fir_col">Association between tobacco substance usage and a missense mutation in the tumor suppressor gene P53 in the Saudi Arabian population.</td>
|
||
<td>Almutairi MH et al.</td>
|
||
<td>2021</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33555293"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33555293</a>
|
||
</td>
|
||
<td class="fir_col">Effect of the p53 P72R Polymorphism on Mutant TP53 Allele Selection in Human Cancer.</td>
|
||
<td>De Souza C et al.</td>
|
||
<td>2021</td>
|
||
<td>Journal of the National Cancer Institute</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33720087"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33720087</a>
|
||
</td>
|
||
<td class="fir_col">Pediatric Non-Alcoholic Fatty Liver Disease Is Affected by Genetic Variants Involved in Lifespan/Healthspan.</td>
|
||
<td>Crudele A et al.</td>
|
||
<td>2021</td>
|
||
<td>Journal of pediatric gastroenterology and nutrition</td>
|
||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33767783"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33767783</a>
|
||
</td>
|
||
<td class="fir_col">Relationship between TP53 and interleukin-6 gene variants and the risk of types 1 and 2 diabetes mellitus development in the Kermanshah province.</td>
|
||
<td>Haghnazari L et al.</td>
|
||
<td>2021</td>
|
||
<td>Journal of medicine and life</td>
|
||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33797738"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33797738</a>
|
||
</td>
|
||
<td class="fir_col">Association Between Genetic Variants in the lncRNA-p53 Regulatory Network and Ischemic Stroke Prognosis.</td>
|
||
<td>Liu X et al.</td>
|
||
<td>2021</td>
|
||
<td>Neurotoxicity research</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33883929"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33883929</a>
|
||
</td>
|
||
<td class="fir_col">Risk of Colorectal Carcinoma May Predispose to the Genetic Variants of the GST, CYP450, and TP53 Genes Among Nonsmokers in the Saudi Community.</td>
|
||
<td>Sindi IA et al.</td>
|
||
<td>2021</td>
|
||
<td>International journal of general medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33906323"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33906323</a>
|
||
</td>
|
||
<td class="fir_col">The Association of Aging-Related Polymorphisms with Susceptibility to Lung Cancer: A Case-Control Study in a Japanese Population.</td>
|
||
<td>Furuie H et al.</td>
|
||
<td>2021</td>
|
||
<td>Asian Pacific journal of cancer prevention </td>
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</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33941312"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33941312</a>
|
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</td>
|
||
<td class="fir_col">Whole-genome sequencing analysis of semi-supercentenarians.</td>
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||
<td>Garagnani P et al.</td>
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||
<td>2021</td>
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<td>eLife</td>
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</tr>
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|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33942220"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33942220</a>
|
||
</td>
|
||
<td class="fir_col">Male and female breast cancer: the two faces of the same genetic susceptibility coin.</td>
|
||
<td>Silva SN et al.</td>
|
||
<td>2021</td>
|
||
<td>Breast cancer research and treatment</td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33959694"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33959694</a>
|
||
</td>
|
||
<td class="fir_col">The cell cycle regulatory gene polymorphisms TP53 (rs1042522) and MDM2 (rs2279744) in lung cancer: a meta-analysis.</td>
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||
<td>Bulgakova O et al.</td>
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||
<td>2020</td>
|
||
<td>Vavilovskii zhurnal genetiki i selektsii</td>
|
||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34077778"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34077778</a>
|
||
</td>
|
||
<td class="fir_col">Polymorphisms in the TP53-MDM2-MDM4-axis in patients with rheumatoid arthritis.</td>
|
||
<td>Gansmo LB et al.</td>
|
||
<td>2021</td>
|
||
<td>Gene</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34131278"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34131278</a>
|
||
</td>
|
||
<td class="fir_col">Genetic polymorphisms associated with obesity in the Arab world: a systematic review.</td>
|
||
<td>Younes S et al.</td>
|
||
<td>2021</td>
|
||
<td>International journal of obesity (2005)</td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34190520"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34190520</a>
|
||
</td>
|
||
<td class="fir_col">A variant of TP53 gene (rs 1625895, 13494g>A) is associated with neoplasm localization in patients with uterine leiomyoma.</td>
|
||
<td>Kornatska AG et al.</td>
|
||
<td>2021</td>
|
||
<td>Experimental oncology</td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34227093"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34227093</a>
|
||
</td>
|
||
<td class="fir_col">Crosstalk of Cyclin-dependent kinase inhibitor 1A (CDKN1A) gene polymorphism with p53 and CCND1 polymorphism in breast cancer.</td>
|
||
<td>Akhter N et al.</td>
|
||
<td>2021</td>
|
||
<td>European review for medical and pharmacological sciences</td>
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||
</tr>
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||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34272429"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34272429</a>
|
||
</td>
|
||
<td class="fir_col">A comprehensive meta-analysis and a case-control study give insights into genetic susceptibility of lung cancer and subgroups.</td>
|
||
<td>Sengupta D et al.</td>
|
||
<td>2021</td>
|
||
<td>Scientific reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34284087"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34284087</a>
|
||
</td>
|
||
<td class="fir_col">Ethnicity-stratified analysis of the association between P53 rs1042522 polymorphism and women HPV infection: A meta-analysis.</td>
|
||
<td>Si D et al.</td>
|
||
<td>2021</td>
|
||
<td>Microbial pathogenesis</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34307186"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34307186</a>
|
||
</td>
|
||
<td class="fir_col">Functional Polymorphisms in the p53 Pathway Genes on the Genetic Susceptibility to Zika Virus Teratogenesis.</td>
|
||
<td>Gomes JA et al.</td>
|
||
<td>2021</td>
|
||
<td>Frontiers in cellular and infection microbiology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34319543"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34319543</a>
|
||
</td>
|
||
<td class="fir_col">Genetic analysis of colorectal carcinoma using high throughput single nucleotide polymorphism genotyping technique within the population of Jammu and Kashmir.</td>
|
||
<td>Sharma B et al.</td>
|
||
<td>2021</td>
|
||
<td>Molecular biology reports</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34386081"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34386081</a>
|
||
</td>
|
||
<td class="fir_col">Role of CXCL12, TP53 and CYP1A1 gene polymorphisms in susceptibility to pediatric acute lymphoblastic leukemia.</td>
|
||
<td>Kampouraki E et al.</td>
|
||
<td>2021</td>
|
||
<td>Oncology letters</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34393505"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34393505</a>
|
||
</td>
|
||
<td class="fir_col">Different Roles of TP53 Codon 72 Polymorphism in Type 2 Diabetes and Its Complications: Evidence from a Case-Control Study on a Chinese Han Population.</td>
|
||
<td>Guo D et al.</td>
|
||
<td>2021</td>
|
||
<td>International journal of general medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34441352"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34441352</a>
|
||
</td>
|
||
<td class="fir_col">The Investigation of Associations between TP53 rs1042522, BBC3 rs2032809, CCND1 rs9344, EGFR rs2227983 Polymorphisms and Breast Cancer Phenotype and Prognosis.</td>
|
||
<td>Bekampytė J et al.</td>
|
||
<td>2021</td>
|
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<td>Diagnostics (Basel, Switzerland)</td>
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</tr>
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||
|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/34478609"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34478609</a>
|
||
</td>
|
||
<td class="fir_col">In search of TP53 mutational hot spots for Li-Fraumeni syndrome in Asian populations.</td>
|
||
<td>Lo Piccolo L et al.</td>
|
||
<td>2021</td>
|
||
<td>Tropical medicine & international health </td>
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</tr>
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||
|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/34540891"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34540891</a>
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</td>
|
||
<td class="fir_col">Umbrella Review on Associations Between Single Nucleotide Polymorphisms and Lung Cancer Risk.</td>
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||
<td>Li X et al.</td>
|
||
<td>2021</td>
|
||
<td>Frontiers in molecular biosciences</td>
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</tr>
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|
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<tr>
|
||
<td><a target="_blank" href="/pubmed/34576245"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">34576245</a>
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</td>
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||
<td class="fir_col">Biomolecular Markers of Recurrent Implantation Failure-A Review.</td>
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||
<td>Mrozikiewicz AE et al.</td>
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||
<td>2021</td>
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||
<td>International journal of molecular sciences</td>
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</tr>
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<tr>
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||
<td><a target="_blank" href="/pubmed/34591432"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">34591432</a>
|
||
</td>
|
||
<td class="fir_col">Association of lipoprotein lipase expression with TP53 gene polymorphisms in chronic lymphocytic leukemia cells.</td>
|
||
<td>Abramenko I et al.</td>
|
||
<td>2021</td>
|
||
<td>Experimental oncology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34606635"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34606635</a>
|
||
</td>
|
||
<td class="fir_col">Effect of NPC1L1 polymorphism on warfarin stable dose in Chinese patients under heart valve replacement surgery.</td>
|
||
<td>Ma S et al.</td>
|
||
<td>2022</td>
|
||
<td>Clinical and experimental pharmacology & physiology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34618298"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">34618298</a>
|
||
</td>
|
||
<td class="fir_col">Genetic variants in the p53 pathway influence implantation and pregnancy maintenance in IVF treatments using donor oocytes.</td>
|
||
<td>Palomares AR et al.</td>
|
||
<td>2021</td>
|
||
<td>Journal of assisted reproduction and genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34683108"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">34683108</a>
|
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</td>
|
||
<td class="fir_col">Targeted Next-Generation Sequencing for the Identification of Genetic Predictors of Radiation-Induced Late Skin Toxicity in Breast Cancer Patients: A Preliminary Study.</td>
|
||
<td>Cargnin S et al.</td>
|
||
<td>2021</td>
|
||
<td>Journal of personalized medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34783250"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34783250</a>
|
||
</td>
|
||
<td class="fir_col">Whole-exome sequencing reveals novel candidate single nucleotide variations for preventing adverse effects of levonorgestrel implantation.</td>
|
||
<td>Zhu W et al.</td>
|
||
<td>2021</td>
|
||
<td>Pharmacogenomics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34783301"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34783301</a>
|
||
</td>
|
||
<td class="fir_col">Anthracycline-induced cardiotoxicity in women without cardiovascular diseases: molecular and genetic predictors.</td>
|
||
<td>Kopeva KV et al.</td>
|
||
<td>2022</td>
|
||
<td>Acta cardiologica</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34916119"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34916119</a>
|
||
</td>
|
||
<td class="fir_col">Genome-wide gene and serum ferritin interaction in the development of type 2 diabetes in adults aged 40 years or older.</td>
|
||
<td>Kim J et al.</td>
|
||
<td>2022</td>
|
||
<td>Nutrition, metabolism, and cardiovascular diseases </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34995174"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34995174</a>
|
||
</td>
|
||
<td class="fir_col">ATM and TP53 polymorphisms modified susceptibility to radiation-induced lens opacity in natural high background radiation area, China.</td>
|
||
<td>Gao Y et al.</td>
|
||
<td>2022</td>
|
||
<td>International journal of radiation biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35038823"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">35038823</a>
|
||
</td>
|
||
<td class="fir_col">Genomic Correlates of Unfavorable Outcome in Locally Advanced Cervical Cancer Treated with Neoadjuvant Chemoradiation.</td>
|
||
<td>Wei Y et al.</td>
|
||
<td>2022</td>
|
||
<td>Cancer research and treatment</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35123410"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">35123410</a>
|
||
</td>
|
||
<td class="fir_col">Importance of TP53 codon 72 and intron 3 duplication 16 bp polymorphisms and their haplotypes in susceptibility to sarcopenia in Iranian older adults.</td>
|
||
<td>Montazeri-Najafabady N et al.</td>
|
||
<td>2022</td>
|
||
<td>BMC geriatrics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35342856"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">35342856</a>
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</td>
|
||
<td class="fir_col">Association between ТР53, MDM2 and NQO1 gene polymorphisms and viral load among women with human papillomavirus.</td>
|
||
<td>AlBosale AH et al.</td>
|
||
<td>2022</td>
|
||
<td>Vavilovskii zhurnal genetiki i selektsii</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35351459"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">35351459</a>
|
||
</td>
|
||
<td class="fir_col">TP53 common variants and interaction with PPP1R13L and CD3EAP SNPs and lung cancer risk and smoking behavior in a Chinese population.</td>
|
||
<td>Yin J et al.</td>
|
||
<td>2022</td>
|
||
<td>Biomedical journal</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35364453"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">35364453</a>
|
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</td>
|
||
<td class="fir_col">Smoking is associated with age at disease onset in Parkinson's disease.</td>
|
||
<td>Rosas I et al.</td>
|
||
<td>2022</td>
|
||
<td>Parkinsonism & related disorders</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35566612"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">35566612</a>
|
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</td>
|
||
<td class="fir_col">Asian Race and Primary Open-Angle Glaucoma: Where Do We Stand?</td>
|
||
<td>Belamkar A et al.</td>
|
||
<td>2022</td>
|
||
<td>Journal of clinical medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35776848"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">35776848</a>
|
||
</td>
|
||
<td class="fir_col">Association between TP53 Arg72Pro variant and recurrent pregnancy loss in the Greek population.</td>
|
||
<td>Dedousi D et al.</td>
|
||
<td>2022</td>
|
||
<td>Hormone molecular biology and clinical investigation</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35801418"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">35801418</a>
|
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</td>
|
||
<td class="fir_col">Mutational landscape of primary breast angiosarcoma with repeated resection and recurrence over a 15-year period: A case report.</td>
|
||
<td>Teruyama F et al.</td>
|
||
<td>2022</td>
|
||
<td>Pathology international</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35872366"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">35872366</a>
|
||
</td>
|
||
<td class="fir_col">Association of ATG16L1 rs2241880 and TP53 rs1042522 with characteristics and course of diffuse large B-cell lymphoma.</td>
|
||
<td>Živanović A et al.</td>
|
||
<td>2022</td>
|
||
<td>Pathology, research and practice</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35984915"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
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data-ga-label="PMID_link">35984915</a>
|
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</td>
|
||
<td class="fir_col">DNA repair in lung cancer: a large-scale quantitative analysis for polymorphisms in DNA repairing pathway genes and lung cancer susceptibility.</td>
|
||
<td>Liao Z et al.</td>
|
||
<td>2022</td>
|
||
<td>Expert review of respiratory medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/35996546"
|
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-section="Publications" data-ga-action="Click-on"
|
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data-ga-label="PMID_link">35996546</a>
|
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</td>
|
||
<td class="fir_col">Association of TP53 rs1042522 C>G Polymorphism with Glioma Risk in Chinese Children.</td>
|
||
<td>Liao F et al.</td>
|
||
<td>2022</td>
|
||
<td>BioMed research international</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/36039053"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-ga-label="PMID_link">36039053</a>
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</td>
|
||
<td class="fir_col">Impact on breast cancer susceptibility and clinicopathological traits of common genetic polymorphisms in TP53, MDM2 and ATM genes in Sardinian women.</td>
|
||
<td>Floris M et al.</td>
|
||
<td>2022</td>
|
||
<td>Oncology letters</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/36059664"
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ref="section=Publications&action=Click-on&label=PMID_link"
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data-ga-label="PMID_link">36059664</a>
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</td>
|
||
<td class="fir_col">Associations of MDM2 rs2279744 and TP53 rs1042522 polymorphisms with cervical cancer risk: A meta-analysis and systematic review.</td>
|
||
<td>Yu M et al.</td>
|
||
<td>2022</td>
|
||
<td>Frontiers in oncology</td>
|
||
</tr>
|
||
|
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</tbody>
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<p id="flanks_tp">The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.</p>
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<option value="option1"
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selected="selected"
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seq_acc_ver="NC_000017.11" position="7676154"
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assmacc="GCF_000001405.40" ref_allele="G"
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GRCh38.p14 ( NC_000017.11 )
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<option value="option2"
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seq_acc_ver="NC_000017.10" position="7579472"
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assmacc="GCF_000001405.25" ref_allele="G"
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variant_type="snv">
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GRCh37.p13 ( NC_000017.10 )
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<option value="option3"
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seq_acc_ver="NG_017013.2" position="16397"
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).<br/>
|
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|
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Visit <a class="external-link" href="/tools/sviewer/" target="_blank">Sequence Viewer</a> for help with navigating inside the display and modifying the selection of displayed data tracks.</p>
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|
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|
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|
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GRCh38.p14 ( NC_000017.11 )
|
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|
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|
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|
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GRCh37.p13 ( NC_000017.10 )
|
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|
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|
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data-assmacc="" data-rsid="1042522">
|
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NG_017013.2
|
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|
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|
||
<script src="/snp/static/django_uswds/uswds/js/uswds.js"></script>
|
||
<script src="/snp/static/snp2redesign/dist/app.bundle.js" type="text/javascript"> </script>
|
||
|
||
|
||
<script src="/snp/static/nwds/js/nwds.js" type="text/javascript"> </script>
|
||
<script src="/snp/static/nwds/js/ncbipopup.js" type="text/javascript"> </script>
|
||
<script src="/snp/static/nwds/js/header.js" type="text/javascript"> </script>
|
||
<script src="/snp/static/nwds/js/ncbiclearbutton.js" type="text/javascript"> </script>
|
||
<script src="/snp/static/nwds/js/override-uswds.js" type="text/javascript"> </script>
|
||
|
||
|
||
|
||
|
||
|
||
<div>Software version is: 2.0.1.post825+45319f0</div>
|
||
|
||
</body>
|
||
</html> |