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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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<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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<h3>Reference SNP (rs) Report</h3>
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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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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/>
|
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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">rs28371706</h2>
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</div>
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</div>
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<div class="accession usa-width-one-third">
|
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<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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|
||
|
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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>chr22:42129770 </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>
|
||
A=0.058268
|
||
(15423/264690, TOPMED)
|
||
</div><div>
|
||
A=0.01306
|
||
(636/48696, ALFA)
|
||
</div><span>
|
||
A=0.05849 (756/12926, GO-ESP)
|
||
</span><span>(<a id="expandfrequency" data-freq-remn="6"
|
||
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">+ 6 more</a>)</span><div class="ui-widget hide_elm" id="remn_summ_freq"><div>
|
||
A=0.0629
|
||
(403/6404, 1000G_30x)
|
||
</div><div>
|
||
A=0.0591
|
||
(296/5008, 1000G)
|
||
</div><div>
|
||
A=0.0027
|
||
(3/1128, Daghestan)
|
||
</div><div>
|
||
A=0.048
|
||
(17/356, PharmGKB)
|
||
</div><div>
|
||
A=0.056
|
||
(12/214, Qatari)
|
||
</div><div>
|
||
G=0.40
|
||
(12/30, SGDP_PRJ)
|
||
</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=((47982[AlleleID]))">ClinVar</a>
|
||
|
||
</dd>
|
||
|
||
|
||
|
||
<dt>Gene : Consequence</dt>
|
||
<dd>
|
||
|
||
<div>CYP2D6 : Missense Variant</div><span>LOC102723722 : 2KB Upstream Variant</span>
|
||
|
||
</dd>
|
||
|
||
<dt>Publications</dt>
|
||
<dd>
|
||
|
||
<a id="snp_pub_count" href="#publications">29
|
||
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">48790</td>
|
||
<td class="popfreq_ref_allele">G=0.98692</td>
|
||
<td class="popfreq_alt_allele">A=0.01308, T=0.00000</td>
|
||
<td class="popfreq_alt_allele">0.975774</td>
|
||
<td class="popfreq_alt_allele">0.001927</td>
|
||
<td class="popfreq_alt_allele">0.0223</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">35378</td>
|
||
<td class="popfreq_ref_allele">G=0.99774</td>
|
||
<td class="popfreq_alt_allele">A=0.00226, T=0.00000</td>
|
||
<td class="popfreq_alt_allele">0.995534</td>
|
||
<td class="popfreq_alt_allele">0.000057</td>
|
||
<td class="popfreq_alt_allele">0.00441</td>
|
||
<td class="popfreq_alt_allele">6</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492703">African</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">5142</td>
|
||
<td class="popfreq_ref_allele">G=0.9107</td>
|
||
<td class="popfreq_alt_allele">A=0.0893, T=0.0000</td>
|
||
<td class="popfreq_alt_allele">0.835084</td>
|
||
<td class="popfreq_alt_allele">0.013613</td>
|
||
<td class="popfreq_alt_allele">0.151303</td>
|
||
<td class="popfreq_alt_allele">7</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492696">African Others</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">148</td>
|
||
<td class="popfreq_ref_allele">G=0.851</td>
|
||
<td class="popfreq_alt_allele">A=0.149, T=0.000</td>
|
||
<td class="popfreq_alt_allele">0.756757</td>
|
||
<td class="popfreq_alt_allele">0.054054</td>
|
||
<td class="popfreq_alt_allele">0.189189</td>
|
||
<td class="popfreq_alt_allele">3</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492698">African American</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">4994</td>
|
||
<td class="popfreq_ref_allele">G=0.9125</td>
|
||
<td class="popfreq_alt_allele">A=0.0875, T=0.0000</td>
|
||
<td class="popfreq_alt_allele">0.837405</td>
|
||
<td class="popfreq_alt_allele">0.012415</td>
|
||
<td class="popfreq_alt_allele">0.15018</td>
|
||
<td class="popfreq_alt_allele">5</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492704">Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">164</td>
|
||
<td class="popfreq_ref_allele">G=1.000</td>
|
||
<td class="popfreq_alt_allele">A=0.000, T=0.000</td>
|
||
<td class="popfreq_alt_allele">1.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">N/A</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492697">East Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">110</td>
|
||
<td class="popfreq_ref_allele">G=1.000</td>
|
||
<td class="popfreq_alt_allele">A=0.000, T=0.000</td>
|
||
<td class="popfreq_alt_allele">1.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">N/A</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492701">Other Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">54</td>
|
||
<td class="popfreq_ref_allele">G=1.00</td>
|
||
<td class="popfreq_alt_allele">A=0.00, T=0.00</td>
|
||
<td class="popfreq_alt_allele">1.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">N/A</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492699">Latin American 1</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">484</td>
|
||
<td class="popfreq_ref_allele">G=0.969</td>
|
||
<td class="popfreq_alt_allele">A=0.031, T=0.000</td>
|
||
<td class="popfreq_alt_allele">0.946281</td>
|
||
<td class="popfreq_alt_allele">0.008264</td>
|
||
<td class="popfreq_alt_allele">0.045455</td>
|
||
<td class="popfreq_alt_allele">8</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492700">Latin American 2</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">612</td>
|
||
<td class="popfreq_ref_allele">G=1.000</td>
|
||
<td class="popfreq_alt_allele">A=0.000, T=0.000</td>
|
||
<td class="popfreq_alt_allele">1.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">N/A</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN10492702">South Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">94</td>
|
||
<td class="popfreq_ref_allele">G=1.00</td>
|
||
<td class="popfreq_alt_allele">A=0.00, T=0.00</td>
|
||
<td class="popfreq_alt_allele">1.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">0.0</td>
|
||
<td class="popfreq_alt_allele">N/A</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN11605645">Other</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">6916</td>
|
||
<td class="popfreq_ref_allele">G=0.9879</td>
|
||
<td class="popfreq_alt_allele">A=0.0121, T=0.0000</td>
|
||
<td class="popfreq_alt_allele">0.978311</td>
|
||
<td class="popfreq_alt_allele">0.002603</td>
|
||
<td class="popfreq_alt_allele">0.019086</td>
|
||
<td class="popfreq_alt_allele">32</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/rs28371706/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=0.941732</td>
|
||
<td>A=0.058268</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">48696</td>
|
||
<td>G=0.98694</td>
|
||
<td>A=0.01306, T=0.00000</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">35302</td>
|
||
<td>G=0.99779</td>
|
||
<td>A=0.00221, 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">6898</td>
|
||
<td>G=0.9878</td>
|
||
<td>A=0.0122, 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">5142</td>
|
||
<td>G=0.9107</td>
|
||
<td>A=0.0893, T=0.0000</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">612</td>
|
||
<td>G=1.000</td>
|
||
<td>A=0.000, T=0.000</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">484</td>
|
||
<td>G=0.969</td>
|
||
<td>A=0.031, T=0.000</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">164</td>
|
||
<td>G=1.000</td>
|
||
<td>A=0.000, 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">94</td>
|
||
<td>G=1.00</td>
|
||
<td>A=0.00, T=0.00</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA192955">GO Exome Sequencing Project</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
Global
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">12926</td>
|
||
<td>G=0.94151</td>
|
||
<td>A=0.05849</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA192955">GO Exome Sequencing Project</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
European American
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">8554</td>
|
||
<td>G=0.9982</td>
|
||
<td>A=0.0018</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA192955">GO Exome Sequencing Project</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
African American
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">4372</td>
|
||
<td>G=0.8305</td>
|
||
<td>A=0.1695</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=0.9363</td>
|
||
<td>A=0.0629, T=0.0008</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=0.7800</td>
|
||
<td>A=0.2200, T=0.0000</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=0.9976</td>
|
||
<td>A=0.0024, T=0.0000</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=1.0000</td>
|
||
<td>A=0.0000, T=0.0000</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=1.0000</td>
|
||
<td>A=0.0000, T=0.0000</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=0.988</td>
|
||
<td>A=0.007, T=0.005</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=0.9409</td>
|
||
<td>A=0.0591</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=0.7821</td>
|
||
<td>A=0.2179</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=1.0000</td>
|
||
<td>A=0.0000</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=0.9980</td>
|
||
<td>A=0.0020</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=1.000</td>
|
||
<td>A=0.000</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=0.991</td>
|
||
<td>A=0.009</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="par_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13013121">Global</a>
|
||
|
||
</td>
|
||
<td>Study-wide</td>
|
||
<td class="samp_s">1128</td>
|
||
<td>G=0.9973</td>
|
||
<td>A=0.0027</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13013126">Daghestan</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">624</td>
|
||
<td>G=1.000</td>
|
||
<td>A=0.000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13013123">Near_East</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">140</td>
|
||
<td>G=0.979</td>
|
||
<td>A=0.021</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13013124">Central Asia</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">122</td>
|
||
<td>G=1.000</td>
|
||
<td>A=0.000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13013127">Europe</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">108</td>
|
||
<td>G=1.000</td>
|
||
<td>A=0.000</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13013122">South Asian</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">98</td>
|
||
<td>G=1.00</td>
|
||
<td>A=0.00</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA576826">Genome-wide autozygosity in Daghestan</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13013125">Caucasus</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">36</td>
|
||
<td>G=1.00</td>
|
||
<td>A=0.00</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">356</td>
|
||
<td>G=0.952</td>
|
||
<td>A=0.048</td>
|
||
</tr>
|
||
|
||
<tr class="chi_row">
|
||
<td>
|
||
|
||
<a href="/bioproject/PRJNA60817">PharmGKB Aggregated</a>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
<a href="/biosample/SAMN13100699">PA149584071</a>
|
||
|
||
</td>
|
||
<td>Sub</td>
|
||
<td class="samp_s">356</td>
|
||
<td>G=0.952</td>
|
||
<td>A=0.048</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">214</td>
|
||
<td>G=0.944</td>
|
||
<td>A=0.056</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">30</td>
|
||
<td>G=0.40</td>
|
||
<td>A=0.57, T=0.03</td>
|
||
</tr>
|
||
|
||
|
||
</tbody>
|
||
</table>
|
||
</div>
|
||
|
||
|
||
</div>
|
||
<div id="variant_details" class="js-tabcontent">
|
||
<a data-width="640px" href="#variant_details_tp"
|
||
ref="section=Variant Details&action=Click-on-Tooltip&label=variant_details_tp"
|
||
data-section="Variant Details" data-ga-action="Click-on-Tooltip"
|
||
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 22</td>
|
||
<td>NC_000022.11:g.42129770G>A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22</td>
|
||
<td>NC_000022.11:g.42129770G>C</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22</td>
|
||
<td>NC_000022.11:g.42129770G>T</td>
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td>gene/pseudogene RefSeqGene (LRG_303)</td>
|
||
<td>NG_008376.4:g.6041C>T</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>gene/pseudogene RefSeqGene (LRG_303)</td>
|
||
<td>NG_008376.4:g.6041C>G</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>gene/pseudogene RefSeqGene (LRG_303)</td>
|
||
<td>NG_008376.4:g.6041C>A</td>
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1</td>
|
||
<td>NW_015148968.1:g.7511G>A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1</td>
|
||
<td>NW_015148968.1:g.7511G>C</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1</td>
|
||
<td>NW_015148968.1:g.7511G>T</td>
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1</td>
|
||
<td>NW_014040931.1:g.23359G>A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1</td>
|
||
<td>NW_014040931.1:g.23359G>C</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1</td>
|
||
<td>NW_014040931.1:g.23359G>T</td>
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1</td>
|
||
<td>NW_009646208.1:g.15336G>A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1</td>
|
||
<td>NW_009646208.1:g.15336G>C</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1</td>
|
||
<td>NW_009646208.1:g.15336G>T</td>
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1</td>
|
||
<td>NW_004504305.1:g.52097G>A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1</td>
|
||
<td>NW_004504305.1:g.52097G>C</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1</td>
|
||
<td>NW_004504305.1:g.52097G>T</td>
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1</td>
|
||
<td>NT_187682.1:g.52111G>A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1</td>
|
||
<td>NT_187682.1:g.52111G>C</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1</td>
|
||
<td>NT_187682.1:g.52111G>T</td>
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td>GRCh37.p13 chr 22</td>
|
||
<td>NC_000022.10:g.42525772G>A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh37.p13 chr 22</td>
|
||
<td>NC_000022.10:g.42525772G>C</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>GRCh37.p13 chr 22</td>
|
||
<td>NC_000022.10:g.42525772G>T</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/1565">CYP2D6</a>, cytochrome P450 family 2 subfamily D member 6
|
||
(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>CYP2D6 transcript variant 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_000106.6:c.320C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">T [</span><span class="codon-ghost">A</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > I [</span><span class="codon-ghost">A</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>cytochrome P450 2D6 isoform 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_000097.3:p.Thr107Ile
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
T (Thr) > I (Ile)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>CYP2D6 transcript variant 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_000106.6:c.320C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">T [</span><span class="codon-ghost">A</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > S [</span><span class="codon-ghost">A</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>cytochrome P450 2D6 isoform 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_000097.3:p.Thr107Ser
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
T (Thr) > S (Ser)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>CYP2D6 transcript variant 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_000106.6:c.320C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">T [</span><span class="codon-ghost">A</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > N [</span><span class="codon-ghost">A</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>cytochrome P450 2D6 isoform 1</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_000097.3:p.Thr107Asn
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
T (Thr) > N (Asn)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>CYP2D6 transcript variant 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001025161.3:c.320C>T
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">T [</span><span class="codon-ghost">A</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > I [</span><span class="codon-ghost">A</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>cytochrome P450 2D6 isoform 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001020332.2:p.Thr107Ile
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
T (Thr) > I (Ile)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_odd">
|
||
<td>CYP2D6 transcript variant 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001025161.3:c.320C>G
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">T [</span><span class="codon-ghost">A</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > S [</span><span class="codon-ghost">A</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>cytochrome P450 2D6 isoform 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001020332.2:p.Thr107Ser
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
T (Thr) > S (Ser)
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
|
||
Missense Variant
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
|
||
<tr class="vard_even">
|
||
<td>CYP2D6 transcript variant 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NM_001025161.3:c.320C>A
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span><span class="codon-plain">T [</span><span class="codon-ghost">A</span><span class="codon-hilite">C</span><span class="codon-ghost">C</span><span class="codon-plain">] > N [</span><span class="codon-ghost">A</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>cytochrome P450 2D6 isoform 2</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
NP_001020332.2:p.Thr107Asn
|
||
|
||
</span>
|
||
</td>
|
||
<td>
|
||
<span>
|
||
|
||
|
||
T (Thr) > N (Asn)
|
||
|
||
</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: A (allele ID:
|
||
<a ref="section=Clinical Significance&action=Click-on&label=allele_link"
|
||
target="_blank" href="/clinvar?term=(47982[AlleleID])"
|
||
data-section="Clinical Significance"
|
||
data-ga-action="Click-on"
|
||
data-ga-label="allele_link">
|
||
47982
|
||
</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/RCV000734612.6">RCV000734612.6</a>
|
||
</td>
|
||
<td>not provided</td>
|
||
<td>Likely-Benign,Other</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/RCV001030445.2">RCV001030445.2</a>
|
||
</td>
|
||
<td>Deutetrabenazine response</td>
|
||
<td>Drug-Response</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/RCV001093718.2">RCV001093718.2</a>
|
||
</td>
|
||
<td>Tamoxifen response</td>
|
||
<td>Drug-Response</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 22
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000022.11:g.42129770=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000022.11:g.42129770G>A
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000022.11:g.42129770G>C
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000022.11:g.42129770G>T
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
gene/pseudogene RefSeqGene (LRG_303)
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NG_008376.4:g.6041=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NG_008376.4:g.6041C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NG_008376.4:g.6041C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NG_008376.4:g.6041C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
CYP2D6 transcript variant 1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000106.6:c.320=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000106.6:c.320C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000106.6:c.320C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000106.6:c.320C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
CYP2D6 transcript variant 1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000106.5:c.320=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000106.5:c.320C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000106.5:c.320C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_000106.5:c.320C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
CYP2D6 transcript variant 2
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001025161.3:c.320=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001025161.3:c.320C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001025161.3:c.320C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001025161.3:c.320C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
CYP2D6 transcript variant 2
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001025161.2:c.320=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001025161.2:c.320C>T
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001025161.2:c.320C>G
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NM_001025161.2:c.320C>A
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
GRCh38.p14 chr 22 novel patch HSCHR22_8_CTG1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_015148968.1:g.7511=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_015148968.1:g.7511G>A
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_015148968.1:g.7511G>C
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_015148968.1:g.7511G>T
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
GRCh38.p14 chr 22 novel patch HSCHR22_7_CTG1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_014040931.1:g.23359=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_014040931.1:g.23359G>A
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_014040931.1:g.23359G>C
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_014040931.1:g.23359G>T
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
GRCh38.p14 chr 22 novel patch HSCHR22_5_CTG1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_009646208.1:g.15336=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_009646208.1:g.15336G>A
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_009646208.1:g.15336G>C
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_009646208.1:g.15336G>T
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
GRCh38.p14 chr 22 alt locus HSCHR22_2_CTG1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_004504305.1:g.52097=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_004504305.1:g.52097G>A
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_004504305.1:g.52097G>C
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NW_004504305.1:g.52097G>T
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
GRCh38.p14 chr 22 alt locus HSCHR22_3_CTG1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NT_187682.1:g.52111=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NT_187682.1:g.52111G>A
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NT_187682.1:g.52111G>C
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NT_187682.1:g.52111G>T
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
GRCh37.p13 chr 22
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000022.10:g.42525772=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000022.10:g.42525772G>A
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000022.10:g.42525772G>C
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NC_000022.10:g.42525772G>T
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cytochrome P450 2D6 isoform 1
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_000097.3:p.Thr107=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_000097.3:p.Thr107Ile
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_000097.3:p.Thr107Ser
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_000097.3:p.Thr107Asn
|
||
</td>
|
||
|
||
</tr>
|
||
|
||
|
||
|
||
<tr>
|
||
<td class="alias_hgvs">
|
||
|
||
cytochrome P450 2D6 isoform 2
|
||
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001020332.2:p.Thr107=
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001020332.2:p.Thr107Ile
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001020332.2:p.Thr107Ser
|
||
</td>
|
||
|
||
<td class="alias_hgvs">
|
||
NP_001020332.2:p.Thr107Asn
|
||
</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">
|
||
|
||
58 SubSNP,
|
||
|
||
19 Frequency,
|
||
|
||
3 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>
|
||
|
||
BIOVENTURES
|
||
|
||
</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=ss32476039">ss32476039</a>
|
||
|
||
</td>
|
||
<td>May 24, 2005
|
||
(125)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>2</td>
|
||
<td>
|
||
|
||
PHARMGKB_AB_DME
|
||
|
||
</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=ss84158076">ss84158076</a>
|
||
|
||
</td>
|
||
<td>Dec 15, 2007
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>3</td>
|
||
<td>
|
||
|
||
CORNELL
|
||
|
||
</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=ss86241437">ss86241437</a>
|
||
|
||
</td>
|
||
<td>Mar 23, 2008
|
||
(129)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>4</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=ss105440153">ss105440153</a>
|
||
|
||
</td>
|
||
<td>Feb 05, 2009
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>5</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=ss114257423">ss114257423</a>
|
||
|
||
</td>
|
||
<td>Jan 25, 2009
|
||
(130)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>6</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=ss159831286">ss159831286</a>
|
||
|
||
</td>
|
||
<td>Dec 01, 2009
|
||
(131)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>7</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=ss169359480">ss169359480</a>
|
||
|
||
</td>
|
||
<td>Jul 04, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>8</td>
|
||
<td>
|
||
|
||
BUSHMAN
|
||
|
||
</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=ss204099761">ss204099761</a>
|
||
|
||
</td>
|
||
<td>Jul 04, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>9</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=ss228698362">ss228698362</a>
|
||
|
||
</td>
|
||
<td>Jul 14, 2010
|
||
(132)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>10</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=ss342544636">ss342544636</a>
|
||
|
||
</td>
|
||
<td>May 09, 2011
|
||
(134)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>11</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=ss491194354">ss491194354</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>12</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=ss491572625">ss491572625</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>13</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=ss491825746">ss491825746</a>
|
||
|
||
</td>
|
||
<td>May 04, 2012
|
||
(137)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>14</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=ss566667084">ss566667084</a>
|
||
|
||
</td>
|
||
<td>Apr 25, 2013
|
||
(138)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>15</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=ss1067607087">ss1067607087</a>
|
||
|
||
</td>
|
||
<td>Aug 21, 2014
|
||
(142)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>16</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=ss1367336211">ss1367336211</a>
|
||
|
||
</td>
|
||
<td>Aug 21, 2014
|
||
(142)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>17</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=ss1397786150">ss1397786150</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>18</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=ss1457608664">ss1457608664</a>
|
||
|
||
</td>
|
||
<td>Nov 23, 2014
|
||
(136)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>19</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=ss1694379589">ss1694379589</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>20</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=ss1694379590">ss1694379590</a>
|
||
|
||
</td>
|
||
<td>Apr 01, 2015
|
||
(144)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>21</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=ss1809806582">ss1809806582</a>
|
||
|
||
</td>
|
||
<td>Sep 08, 2015
|
||
(146)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>22</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=ss1938961307">ss1938961307</a>
|
||
|
||
</td>
|
||
<td>Feb 12, 2016
|
||
(147)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>23</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=ss1959984049">ss1959984049</a>
|
||
|
||
</td>
|
||
<td>Feb 12, 2016
|
||
(147)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>24</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=ss2030253499">ss2030253499</a>
|
||
|
||
</td>
|
||
<td>Sep 14, 2016
|
||
(149)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>25</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=ss2745192102">ss2745192102</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>26</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=ss2750571830">ss2750571830</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>27</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=ss2974893852">ss2974893852</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>28</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=ss2985240512">ss2985240512</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>29</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=ss2985857677">ss2985857677</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>30</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=ss3022190905">ss3022190905</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>31</td>
|
||
<td>
|
||
|
||
CSIRBIOHTS
|
||
|
||
</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=ss3029638778">ss3029638778</a>
|
||
|
||
</td>
|
||
<td>Nov 08, 2017
|
||
(151)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>32</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=ss3652655257">ss3652655257</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>33</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=ss3654008766">ss3654008766</a>
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>34</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=ss3708287386">ss3708287386</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>35</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=ss3822593693">ss3822593693</a>
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>36</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=ss3825454887">ss3825454887</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>37</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=ss3890637723">ss3890637723</a>
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>38</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=ss3984237335">ss3984237335</a>
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>39</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=ss3986866498">ss3986866498</a>
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>40</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=ss5110781171">ss5110781171</a>
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>41</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=ss5232837247">ss5232837247</a>
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>42</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=ss5232837248">ss5232837248</a>
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>43</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=ss5237618467">ss5237618467</a>
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>44</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=ss5237618468">ss5237618468</a>
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>45</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=ss5311255713">ss5311255713</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>46</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=ss5441587728">ss5441587728</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>47</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=ss5503082737">ss5503082737</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>48</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=ss5503082738">ss5503082738</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>49</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=ss5512474031">ss5512474031</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>50</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=ss5618884899">ss5618884899</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>51</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=ss5624504246">ss5624504246</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>52</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=ss5664576761">ss5664576761</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>53</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=ss5794029239">ss5794029239</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>54</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=ss5794029240">ss5794029240</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>55</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=ss5822131258">ss5822131258</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>56</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=ss5847519180">ss5847519180</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>57</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=ss5847946441">ss5847946441</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>58</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=ss5959434939">ss5959434939</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>59</td>
|
||
<td>
|
||
|
||
1000Genomes
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000022.10 - 42525772
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>60</td>
|
||
<td>
|
||
|
||
1000Genomes_30x
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000022.11 - 42129770
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>61</td>
|
||
<td>
|
||
|
||
Genome-wide autozygosity in Daghestan
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000022.9 - 40855716
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>62</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_62"
|
||
data-ga-label="submission_tt_62" class="disabled">
|
||
ExAC
|
||
</a>
|
||
<p id="submission_tt_62" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 5962913 (NC_000022.10:42525771:G:G 112534/114558, NC_000022.10:42525771:G:A 2024/114558)<br>Row 5962914 (NC_000022.10:42525771:G:G 114467/114558, NC_000022.10:42525771:G:T 91/114558)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>63</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_63"
|
||
data-ga-label="submission_tt_63" class="disabled">
|
||
ExAC
|
||
</a>
|
||
<p id="submission_tt_63" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 5962913 (NC_000022.10:42525771:G:G 112534/114558, NC_000022.10:42525771:G:A 2024/114558)<br>Row 5962914 (NC_000022.10:42525771:G:G 114467/114558, NC_000022.10:42525771:G:T 91/114558)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>64</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_64"
|
||
data-ga-label="submission_tt_64" class="disabled">
|
||
gnomAD - Genomes
|
||
</a>
|
||
<p id="submission_tt_64" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 571270367 (NC_000022.11:42129769:G:A 7848/139348)<br>Row 571270368 (NC_000022.11:42129769:G:T 111/139370)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>65</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_65"
|
||
data-ga-label="submission_tt_65" class="disabled">
|
||
gnomAD - Genomes
|
||
</a>
|
||
<p id="submission_tt_65" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 571270367 (NC_000022.11:42129769:G:A 7848/139348)<br>Row 571270368 (NC_000022.11:42129769:G:T 111/139370)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>66</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_66"
|
||
data-ga-label="submission_tt_66" class="disabled">
|
||
gnomAD - Exomes
|
||
</a>
|
||
<p id="submission_tt_66" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 14524906 (NC_000022.10:42525771:G:G 240739/244170, NC_000022.10:42525771:G:A 3431/244170)<br>Row 14524907 (NC_000022.10:42525771:G:G 244130/244170, NC_000022.10:42525771:G:T 40/244170)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>67</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_67"
|
||
data-ga-label="submission_tt_67" class="disabled">
|
||
gnomAD - Exomes
|
||
</a>
|
||
<p id="submission_tt_67" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 14524906 (NC_000022.10:42525771:G:G 240739/244170, NC_000022.10:42525771:G:A 3431/244170)<br>Row 14524907 (NC_000022.10:42525771:G:G 244130/244170, NC_000022.10:42525771:G:T 40/244170)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Jul 13, 2019
|
||
(153)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>68</td>
|
||
<td>
|
||
|
||
GO Exome Sequencing Project
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000022.10 - 42525772
|
||
|
||
</td>
|
||
<td>Oct 12, 2018
|
||
(152)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>69</td>
|
||
<td>
|
||
|
||
PharmGKB Aggregated
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000022.11 - 42129770
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>70</td>
|
||
<td>
|
||
|
||
Qatari
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000022.10 - 42525772
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>71</td>
|
||
<td>
|
||
|
||
SGDP_PRJ
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000022.10 - 42525772
|
||
|
||
</td>
|
||
<td>Apr 27, 2020
|
||
(154)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>72</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_72"
|
||
data-ga-label="submission_tt_72" class="disabled">
|
||
8.3KJPN
|
||
</a>
|
||
<p id="submission_tt_72" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 90806554 (NC_000022.10:42525771:G:C 1/16716)<br>Row 90806555 (NC_000022.10:42525771:G:T 2/16716)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>73</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_73"
|
||
data-ga-label="submission_tt_73" class="disabled">
|
||
8.3KJPN
|
||
</a>
|
||
<p id="submission_tt_73" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 90806554 (NC_000022.10:42525771:G:C 1/16716)<br>Row 90806555 (NC_000022.10:42525771:G:T 2/16716)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>74</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_74"
|
||
data-ga-label="submission_tt_74" class="disabled">
|
||
14KJPN
|
||
</a>
|
||
<p id="submission_tt_74" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 127866343 (NC_000022.11:42129769:G:C 1/28172)<br>Row 127866344 (NC_000022.11:42129769:G:T 4/28172)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr class="disabled" >
|
||
<td>75</td>
|
||
<td>
|
||
|
||
<a href="#submission_tt_75"
|
||
data-ga-label="submission_tt_75" class="disabled">
|
||
14KJPN
|
||
</a>
|
||
<p id="submission_tt_75" class="break_values">
|
||
Submission ignored due to conflicting rows:<br>Row 127866343 (NC_000022.11:42129769:G:C 1/28172)<br>Row 127866344 (NC_000022.11:42129769:G:T 4/28172)
|
||
</p>
|
||
|
||
</td>
|
||
<td>
|
||
|
||
-
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>76</td>
|
||
<td>
|
||
|
||
TopMed
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000022.11 - 42129770
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>77</td>
|
||
<td>
|
||
|
||
ALFA
|
||
|
||
</td>
|
||
<td>
|
||
|
||
NC_000022.11 - 42129770
|
||
|
||
</td>
|
||
<td>Apr 26, 2021
|
||
(155)
|
||
</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="/clinvar/RCV000734612.6/">RCV000734612.6</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>79</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/RCV001030445.2/">RCV001030445.2</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 2022
|
||
(156)
|
||
</td>
|
||
</tr>
|
||
|
||
<tr >
|
||
<td>80</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/RCV001093718.2/">RCV001093718.2</a>
|
||
|
||
</td>
|
||
<td>Oct 16, 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="rs59604033">rs59604033</a>
|
||
</td>
|
||
<td>May 25, 2008
|
||
(130)
|
||
</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="rs587777915">rs587777915</a>
|
||
</td>
|
||
<td>Feb 02, 2015
|
||
(136)
|
||
</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>
|
||
|
||
300101,
|
||
|
||
ss114257423,
|
||
|
||
ss169359480,
|
||
|
||
ss204099761,
|
||
|
||
ss491825746,
|
||
|
||
ss1397786150
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.9:40855715:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
80894631,
|
||
|
||
1911716,
|
||
|
||
21003229,
|
||
|
||
42654703,
|
||
|
||
ss228698362,
|
||
|
||
ss342544636,
|
||
|
||
ss491194354,
|
||
|
||
ss491572625,
|
||
|
||
ss566667084,
|
||
|
||
ss1067607087,
|
||
|
||
ss1367336211,
|
||
|
||
ss1694379589,
|
||
|
||
ss1809806582,
|
||
|
||
ss1938961307,
|
||
|
||
ss1959984049,
|
||
|
||
ss2030253499,
|
||
|
||
ss2745192102,
|
||
|
||
ss2750571830,
|
||
|
||
ss2974893852,
|
||
|
||
ss2985240512,
|
||
|
||
ss2985857677,
|
||
|
||
ss3022190905,
|
||
|
||
ss3029638778,
|
||
|
||
ss3652655257,
|
||
|
||
ss3654008766,
|
||
|
||
ss3825454887,
|
||
|
||
ss3890637723,
|
||
|
||
ss3984237335,
|
||
|
||
ss3986866498,
|
||
|
||
ss5237618467,
|
||
|
||
ss5237618468,
|
||
|
||
ss5441587728,
|
||
|
||
ss5512474031,
|
||
|
||
ss5624504246,
|
||
|
||
ss5664576761,
|
||
|
||
ss5822131258,
|
||
|
||
ss5847519180,
|
||
|
||
ss5847946441,
|
||
|
||
ss5959434939
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.10:42525771:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
RCV000734612.6,
|
||
|
||
RCV001030445.2,
|
||
|
||
RCV001093718.2,
|
||
|
||
106410834,
|
||
|
||
7684,
|
||
|
||
385890118,
|
||
|
||
10803165722,
|
||
|
||
ss3708287386,
|
||
|
||
ss3822593693,
|
||
|
||
ss5110781171,
|
||
|
||
ss5311255713,
|
||
|
||
ss5503082737,
|
||
|
||
ss5618884899
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
ss32476039,
|
||
|
||
ss84158076,
|
||
|
||
ss86241437,
|
||
|
||
ss105440153,
|
||
|
||
ss159831286
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NT_011520.12:21916340:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
ss1457608664
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NT_011520.13:23420205:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:A
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
ss5232837247
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.10:42525771:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
(self)
|
||
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
ss5794029239
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:C
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td>
|
||
|
||
42654703,
|
||
|
||
ss1694379590,
|
||
|
||
ss2745192102,
|
||
|
||
ss2750571830,
|
||
|
||
ss2974893852,
|
||
|
||
ss3890637723,
|
||
|
||
ss3986866498,
|
||
|
||
ss5232837248,
|
||
|
||
ss5512474031
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.10:42525771:G:T
|
||
|
||
|
||
</td>
|
||
<td>
|
||
|
||
|
||
NC_000022.11:42129769:G:T
|
||
|
||
|
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106410834,
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10803165722,
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ss5503082738,
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ss5618884899,
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ss5794029240
|
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|
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NC_000022.11:42129769:G:T
|
||
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|
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NC_000022.11:42129769:G:T
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|
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|
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|
||
</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"
|
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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">
|
||
29
|
||
citations for rs28371706
|
||
</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/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/19164093"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">19164093</a>
|
||
</td>
|
||
<td class="fir_col">Novel variants of major drug-metabolising enzyme genes in diverse African populations and their predicted functional effects.</td>
|
||
<td>Matimba A et al.</td>
|
||
<td>2009</td>
|
||
<td>Human genomics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21480951"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21480951</a>
|
||
</td>
|
||
<td class="fir_col">Impact of CYP2D6, CYP3A5, CYP2C9 and CYP2C19 polymorphisms on tamoxifen pharmacokinetics in Asian breast cancer patients.</td>
|
||
<td>Lim JS et al.</td>
|
||
<td>2011</td>
|
||
<td>British journal of clinical pharmacology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/21790905"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">21790905</a>
|
||
</td>
|
||
<td class="fir_col">CYP2B6 SNPs are associated with methadone dose required for effective treatment of opioid addiction.</td>
|
||
<td>Levran O et al.</td>
|
||
<td>2013</td>
|
||
<td>Addiction biology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22111602"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22111602</a>
|
||
</td>
|
||
<td class="fir_col">Exploration of CYP450 and drug transporter genotypes and correlations with nevirapine exposure in Malawians.</td>
|
||
<td>Brown KC et al.</td>
|
||
<td>2012</td>
|
||
<td>Pharmacogenomics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/22482072"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">22482072</a>
|
||
</td>
|
||
<td class="fir_col">Genomics of Dementia: APOE- and CYP2D6-Related Pharmacogenetics.</td>
|
||
<td>Cacabelos R et al.</td>
|
||
<td>2012</td>
|
||
<td>International journal of Alzheimer's disease</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/23133420"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">23133420</a>
|
||
</td>
|
||
<td class="fir_col">Pharmacogenomic Diversity among Brazilians: Influence of Ancestry, Self-Reported Color, and Geographical Origin.</td>
|
||
<td>Suarez-Kurtz G et al.</td>
|
||
<td>2012</td>
|
||
<td>Frontiers in pharmacology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/25266489"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">25266489</a>
|
||
</td>
|
||
<td class="fir_col">Genetic polymorphisms of VIP variants in the Tajik ethnic group of northwest China.</td>
|
||
<td>Zhang J et al.</td>
|
||
<td>2014</td>
|
||
<td>BMC genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26091847"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26091847</a>
|
||
</td>
|
||
<td class="fir_col">Genetic polymorphisms of pharmacogenomic VIP variants in the Uygur population from northwestern China.</td>
|
||
<td>Wang L et al.</td>
|
||
<td>2015</td>
|
||
<td>BMC genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26369774"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26369774</a>
|
||
</td>
|
||
<td class="fir_col">Impact of New Genomic Technologies on Understanding Adverse Drug Reactions.</td>
|
||
<td>Maggo SD et al.</td>
|
||
<td>2016</td>
|
||
<td>Clinical pharmacokinetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/26793106"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">26793106</a>
|
||
</td>
|
||
<td class="fir_col">CYP2D7 Sequence Variation Interferes with TaqMan CYP2D6 (*) 15 and (*) 35 Genotyping.</td>
|
||
<td>Riffel AK et al.</td>
|
||
<td>2015</td>
|
||
<td>Frontiers in pharmacology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/27108086"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27108086</a>
|
||
</td>
|
||
<td class="fir_col">Multiplex SNaPshot-a new simple and efficient CYP2D6 and ADRB1 genotyping method.</td>
|
||
<td>Ben S et al.</td>
|
||
<td>2016</td>
|
||
<td>Human genomics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/27233804"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27233804</a>
|
||
</td>
|
||
<td class="fir_col">Genetic polymorphisms of pharmacogenomic VIP variants in the Mongol of Northwestern China.</td>
|
||
<td>Jin T et al.</td>
|
||
<td>2016</td>
|
||
<td>BMC genetics</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/27467145"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27467145</a>
|
||
</td>
|
||
<td class="fir_col">Variation in Human Cytochrome P-450 Drug-Metabolism Genes: A Gateway to the Understanding of Plasmodium vivax Relapses.</td>
|
||
<td>Silvino AC et al.</td>
|
||
<td>2016</td>
|
||
<td>PloS one</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/27785397"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">27785397</a>
|
||
</td>
|
||
<td class="fir_col">CYP2D6 allele distribution in Macedonians, Albanians and Romanies in the Republic of Macedonia.</td>
|
||
<td>Kuzmanovska M et al.</td>
|
||
<td>2015</td>
|
||
<td>Balkan journal of medical genetics </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/28603633"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">28603633</a>
|
||
</td>
|
||
<td class="fir_col">In vitro metabolism of exemestane by hepatic cytochrome P450s: impact of nonsynonymous polymorphisms on formation of the active metabolite 17β-dihydroexemestane.</td>
|
||
<td>Peterson A et al.</td>
|
||
<td>2017</td>
|
||
<td>Pharmacology research & perspectives</td>
|
||
</tr>
|
||
|
||
<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>
|
||
<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>
|
||
<td>Borobia AM et al.</td>
|
||
<td>2018</td>
|
||
<td>Clinical and translational science</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/29681089"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">29681089</a>
|
||
</td>
|
||
<td class="fir_col">Genetic variation in biotransformation enzymes, air pollution exposures, and risk of spina bifida.</td>
|
||
<td>Padula AM et al.</td>
|
||
<td>2018</td>
|
||
<td>American journal of medical genetics. Part A</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/30068618"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">30068618</a>
|
||
</td>
|
||
<td class="fir_col">Cohort Profile: the Predictors of Breast Cancer Recurrence (ProBe CaRE) Premenopausal Breast Cancer Cohort Study in Denmark.</td>
|
||
<td>Collin LJ et al.</td>
|
||
<td>2018</td>
|
||
<td>BMJ open</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/31019283"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31019283</a>
|
||
</td>
|
||
<td class="fir_col">Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests.</td>
|
||
<td>Thauvin-Robinet C et al.</td>
|
||
<td>2019</td>
|
||
<td>European journal of human genetics </td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/31858263"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">31858263</a>
|
||
</td>
|
||
<td class="fir_col">Defining screening panel of functional variants of CYP1A1, CYP2C9, CYP2C19, CYP2D6, and CYP3A4 genes in Serbian population.</td>
|
||
<td>Skadrić I et al.</td>
|
||
<td>2020</td>
|
||
<td>International journal of legal medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32326111"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32326111</a>
|
||
</td>
|
||
<td class="fir_col">Role of Genetic Variations in the Hepatic Handling of Drugs.</td>
|
||
<td>Marin JJG et al.</td>
|
||
<td>2020</td>
|
||
<td>International journal of molecular sciences</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/32639515"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">32639515</a>
|
||
</td>
|
||
<td class="fir_col">Bayesian Pathway Analysis for Complex Interactions.</td>
|
||
<td>Baurley JW et al.</td>
|
||
<td>2020</td>
|
||
<td>American journal of epidemiology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33519226"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33519226</a>
|
||
</td>
|
||
<td class="fir_col">Genetic Diversity of Drug-Related Genes in Native Americans of the Brazilian Amazon.</td>
|
||
<td>Fernandes MR et al.</td>
|
||
<td>2021</td>
|
||
<td>Pharmacogenomics and personalized medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/33875422"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">33875422</a>
|
||
</td>
|
||
<td class="fir_col">Pharmacogene Sequencing of a Gabonese Population with Severe Plasmodium falciparum Malaria Reveals Multiple Novel Variants with Putative Relevance for Antimalarial Treatment.</td>
|
||
<td>Pernaute-Lau L et al.</td>
|
||
<td>2021</td>
|
||
<td>Antimicrobial agents and chemotherapy</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34385834"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34385834</a>
|
||
</td>
|
||
<td class="fir_col">Individualized Drugs' Selection by Evaluation of Drug Properties, Pharmacogenomics and Clinical Parameters: Performance of a Bioinformatic Tool Compared to a Clinically Established Counselling Process.</td>
|
||
<td>Borro M et al.</td>
|
||
<td>2021</td>
|
||
<td>Pharmacogenomics and personalized medicine</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34621706"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34621706</a>
|
||
</td>
|
||
<td class="fir_col">Comprehensive analysis of important pharmacogenes in Koreans using the DMET™ platform.</td>
|
||
<td>Kim B et al.</td>
|
||
<td>2021</td>
|
||
<td>Translational and clinical pharmacology</td>
|
||
</tr>
|
||
|
||
<tr>
|
||
<td><a target="_blank" href="/pubmed/34958284"
|
||
ref="section=Publications&action=Click-on&label=PMID_link"
|
||
data-section="Publications" data-ga-action="Click-on"
|
||
data-ga-label="PMID_link">34958284</a>
|
||
</td>
|
||
<td class="fir_col">Warfarin Pharmacogenomics for Precision Medicine in Real-Life Clinical Practice in Southern Africa: Harnessing 73 Variants in 29 Pharmacogenes.</td>
|
||
<td>Muyambo S et al.</td>
|
||
<td>2022</td>
|
||
<td>Omics </td>
|
||
</tr>
|
||
|
||
</tbody>
|
||
</table>
|
||
|
||
</div>
|
||
<a ref="section=Publications&action=Click-on&label=View_All_link" target="_blank"
|
||
href="/pubmed?term=18547414,19164093,21480951,21790905,22111602,22482072,23133420,25266489,26091847,26369774,26793106,27108086,27233804,27467145,27785397,28603633,29193749,29681089,30068618,30409984,31019283,31858263,32326111,32639515,33519226,33875422,34385834,34621706,34958284"
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|
||
data-ga-label="View_All_link">
|
||
<button class="usa-button-outline" type="button">View All in PubMed</button>
|
||
</a>
|
||
|
||
</div>
|
||
|
||
<div id="flanks" class="js-tabcontent">
|
||
<a data-width="640px" href="#flanks_tp"
|
||
ref="section=Flanks&action=Click-on-Tooltip&label=flanks_tp"
|
||
data-section="Flanks" data-ga-action="Click-on-Tooltip"
|
||
data-ga-label="flanks_tp" class="fa fa-question-circle align-right ncbiPopper">
|
||
<span class="usa-sr-only">Help</span>
|
||
</a>
|
||
<p id="flanks_tp">The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.</p>
|
||
|
||
<div id="flanks_container">
|
||
<div id="context_container">
|
||
<span class="sect_heading">
|
||
Genome context:
|
||
</span>
|
||
|
||
<select id="flank_context">
|
||
|
||
<option value="option1"
|
||
selected="selected"
|
||
seq_acc_ver="NC_000022.11" position="42129770"
|
||
assmacc="GCF_000001405.40" ref_allele="G"
|
||
variant_type="snv">
|
||
|
||
GRCh38.p14 ( NC_000022.11 )
|
||
|
||
</option>
|
||
|
||
<option value="option2"
|
||
|
||
seq_acc_ver="NG_008376.4" position="6041"
|
||
assmacc="" ref_allele="G"
|
||
variant_type="snv">
|
||
|
||
NG_008376.4
|
||
|
||
</option>
|
||
|
||
<option value="option3"
|
||
|
||
seq_acc_ver="NW_015148968.1" position="7511"
|
||
assmacc="GCF_000001405.40" ref_allele="G"
|
||
variant_type="snv">
|
||
|
||
GRCh38.p14 ( NW_015148968.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option4"
|
||
|
||
seq_acc_ver="NW_014040931.1" position="23359"
|
||
assmacc="GCF_000001405.40" ref_allele="G"
|
||
variant_type="snv">
|
||
|
||
GRCh38.p14 ( NW_014040931.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option5"
|
||
|
||
seq_acc_ver="NW_009646208.1" position="15336"
|
||
assmacc="GCF_000001405.40" ref_allele="G"
|
||
variant_type="snv">
|
||
|
||
GRCh38.p14 ( NW_009646208.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option6"
|
||
|
||
seq_acc_ver="NW_004504305.1" position="52097"
|
||
assmacc="GCF_000001405.25" ref_allele="G"
|
||
variant_type="snv">
|
||
|
||
GRCh37.p13 ( NW_004504305.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option7"
|
||
|
||
seq_acc_ver="NW_004504305.1" position="52097"
|
||
assmacc="GCF_000001405.40" ref_allele="G"
|
||
variant_type="snv">
|
||
|
||
GRCh38.p14 ( NW_004504305.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option8"
|
||
|
||
seq_acc_ver="NT_187682.1" position="52111"
|
||
assmacc="GCF_000001405.40" ref_allele="G"
|
||
variant_type="snv">
|
||
|
||
GRCh38.p14 ( NT_187682.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option9"
|
||
|
||
seq_acc_ver="NC_000022.10" position="42525772"
|
||
assmacc="GCF_000001405.25" ref_allele="G"
|
||
variant_type="snv">
|
||
|
||
GRCh37.p13 ( NC_000022.10 )
|
||
|
||
</option>
|
||
|
||
</select>
|
||
</div>
|
||
|
||
|
||
<span class="sect_heading">
|
||
Select flank length:
|
||
</span>
|
||
<select id="flank_length">
|
||
|
||
|
||
<option value="25"
|
||
selected="selected">
|
||
25 nt</option>
|
||
|
||
<option value="50"
|
||
>
|
||
50 nt</option>
|
||
|
||
<option value="100"
|
||
>
|
||
100 nt</option>
|
||
|
||
<option value="200"
|
||
>
|
||
200 nt</option>
|
||
|
||
|
||
</select>
|
||
<button id="retrieve_flank" class="usa-button-outline" type="button">Retrieve</button>
|
||
<div id="flanking_sequence">
|
||
</div>
|
||
</div>
|
||
|
||
|
||
</div>
|
||
</div>
|
||
<div class="usa-row">
|
||
<h3 id="seq_hash" class="green-heading">Genomic regions, transcripts, and products
|
||
<div>
|
||
<span><a href="#top" ref="section=Sequence Viewer&action=Click-on&label=Top_link"
|
||
data-section="Sequence Viewer" data-ga-action="Click-on"
|
||
data-ga-label="Top_link">Top</a></span><span>▲</span>
|
||
<a data-width="640px" href="#sequence_viewer_tp"
|
||
ref="section=Sequence Viewer&action=Click-on-Tooltip&label=sequence_viewer_tp"
|
||
data-section="Sequence Viewer" data-ga-action="Click-on-Tooltip"
|
||
data-ga-label="sequence_viewer_tp" class="fa fa-question-circle align-right ncbiPopper">
|
||
<span class="usa-sr-only">Help</span>
|
||
</a>
|
||
<p id="sequence_viewer_tp">
|
||
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).<br/>
|
||
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.<br/>
|
||
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>
|
||
|
||
</div>
|
||
</h3>
|
||
<div id="sequence">
|
||
|
||
<div id="seq_div" class="usa-width-one-whole">
|
||
<label for="seq_sel">Choose placement</label>
|
||
<select id="seq_sel">
|
||
|
||
<option value="option1"
|
||
selected="selected"
|
||
data-svparams="id=NC_000022.11&assm_context=GCF_000001405.40&v=42129720.0:42129820.0&mk=42129770|rs28371706!&theme=SNP_ref"
|
||
data-assmacc="GCF_000001405.40" data-rsid="28371706">
|
||
|
||
GRCh38.p14 ( NC_000022.11 )
|
||
|
||
</option>
|
||
|
||
<option value="option2"
|
||
|
||
data-svparams="id=NG_008376.4&assm_context=&v=5991.0:6091.0&mk=6041|rs28371706!&theme=SNP_ref"
|
||
data-assmacc="" data-rsid="28371706">
|
||
|
||
NG_008376.4
|
||
|
||
</option>
|
||
|
||
<option value="option3"
|
||
|
||
data-svparams="id=NW_015148968.1&assm_context=GCF_000001405.40&v=7461.0:7561.0&mk=7511|rs28371706!&theme=SNP_ref"
|
||
data-assmacc="GCF_000001405.40" data-rsid="28371706">
|
||
|
||
GRCh38.p14 ( NW_015148968.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option4"
|
||
|
||
data-svparams="id=NW_014040931.1&assm_context=GCF_000001405.40&v=23309.0:23409.0&mk=23359|rs28371706!&theme=SNP_ref"
|
||
data-assmacc="GCF_000001405.40" data-rsid="28371706">
|
||
|
||
GRCh38.p14 ( NW_014040931.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option5"
|
||
|
||
data-svparams="id=NW_009646208.1&assm_context=GCF_000001405.40&v=15286.0:15386.0&mk=15336|rs28371706!&theme=SNP_ref"
|
||
data-assmacc="GCF_000001405.40" data-rsid="28371706">
|
||
|
||
GRCh38.p14 ( NW_009646208.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option6"
|
||
|
||
data-svparams="id=NW_004504305.1&assm_context=GCF_000001405.25&v=52047.0:52147.0&mk=52097|rs28371706!&theme=SNP_ref"
|
||
data-assmacc="GCF_000001405.25" data-rsid="28371706">
|
||
|
||
GRCh37.p13 ( NW_004504305.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option7"
|
||
|
||
data-svparams="id=NW_004504305.1&assm_context=GCF_000001405.40&v=52047.0:52147.0&mk=52097|rs28371706!&theme=SNP_ref"
|
||
data-assmacc="GCF_000001405.40" data-rsid="28371706">
|
||
|
||
GRCh38.p14 ( NW_004504305.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option8"
|
||
|
||
data-svparams="id=NT_187682.1&assm_context=GCF_000001405.40&v=52061.0:52161.0&mk=52111|rs28371706!&theme=SNP_ref"
|
||
data-assmacc="GCF_000001405.40" data-rsid="28371706">
|
||
|
||
GRCh38.p14 ( NT_187682.1 )
|
||
|
||
</option>
|
||
|
||
<option value="option9"
|
||
|
||
data-svparams="id=NC_000022.10&assm_context=GCF_000001405.25&v=42525722.0:42525822.0&mk=42525772|rs28371706!&theme=SNP_ref"
|
||
data-assmacc="GCF_000001405.25" data-rsid="28371706">
|
||
|
||
GRCh37.p13 ( NC_000022.10 )
|
||
|
||
</option>
|
||
|
||
</select>
|
||
<div class="align-right">
|
||
<a href="#"
|
||
ref="section=Sequence Viewer&action=Click-on&label=See_rs_in_Variation_Viewer_link"
|
||
data-section="Sequence Viewer" data-ga-action="Click-on"
|
||
data-ga-label="See_rs_in_Variation_Viewer_link">
|
||
<button title="see rs28371706 and neighboring variants in Variation Viewer"
|
||
class="usa-button-outline" id="variation_viewer_btn" type="button">See rs28371706
|
||
in Variation Viewer
|
||
</button>
|
||
</a>
|
||
</div>
|
||
</div>
|
||
<div class="usa-width-one-whole">
|
||
<div id="sv1" class="SeqViewerApp align-right">
|
||
|
||
<a href="?embedded=true&app_context=Variation_Viewer_2-1&id=NC_000022.11"
|
||
aria-hidden="true"></a>
|
||
</div>
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
|
||
</div>
|
||
|
||
|
||
|
||
|
||
</main>
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</div>
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|
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<script type="text/javascript" src="https://www.ncbi.nlm.nih.gov/core/pinger/pinger.js"> </script>
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