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<h1><a data-section="Header" data-ga-action="Click-on"
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<h3 class="usa-alert-heading">Welcome to the Reference SNP (rs) Report</h3>
<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"
data-ga-action="Click for forward orientation" data-ga-category="Info panel"
data-ga-label="Forward orientation">Forward orientation</a>. Click on the
<a href="#variant_details" id="variantlink"
data-ga-action="Click for variant details" data-ga-category="Info panel"
data-ga-label="Forward orientation">Variant Details tab</a> for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the
<a href="#hgvs_tab" id="hgvslink"
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data-ga-label="HGVS tab">HGVS tab</a>.</p>
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<h3>Reference SNP (rs) Report</h3>
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<ul class="utilities usa-unstyled-list align-right">
<li title="Download in API JSON format"><a href="https://api.ncbi.nlm.nih.gov/variation/v0/refsnp/1801160"
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<p id="main_tp">
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.<br/>
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.<br/>
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors. <br/>
For more information see <a class="external-link" href="/snp/docs/refsnp_report/helpdoc"> Help documentation</a>.</p>
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<h2 id="refsnp_id">rs1801160</h2>
</div>
</div>
<div class="accession usa-width-one-third">
<p>Current Build <span>157</span></p>
<p>Released <span>
September 3, 2024
</span></p>
</div>
</div>
<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>chr1:97305364 </span><span>(GRCh38.p14) </span><a data-width="640px" href="#pos_tp"
ref="section=Summary&action=Click-on-Tooltip&label=pos_tp"
data-section="Summary" data-ga-action="Click-on-Tooltip"
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>
C>A / C>G / C>T
</dd>
<dt>Variation Type</dt>
<dd>
SNV
<span class="small-font gray">Single Nucleotide Variation</span>
</dd>
<dt>Frequency</dt>
<dd>
<div>
T=0.0470975
(65936/1399990, GnomAD_exomes)
</div><div>
T=0.040670
(10765/264690, TOPMED)
</div><span>
T=0.050123 (11993/239272, ALFA)
</span><span>(<a id="expandfrequency" data-freq-remn="24"
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">+ 24 more</a>)</span><div class="ui-widget hide_elm" id="remn_summ_freq"><div>
T=0.039929
(5947/148940, GnomAD_genomes)
</div><div>
T=0.046473
(5630/121146, ExAC)
</div><div>
T=0.03499
(2754/78702, PAGE_STUDY)
</div><div>
T=0.01710
(1324/77428, 38KJPN)
</div><div>
T=0.04137
(538/13006, GO-ESP)
</div><div>
T=0.0200
(145/7232, Korea4K)
</div><div>
T=0.0433
(277/6404, 1000G_30X)
</div><div>
T=0.0439
(220/5008, 1000G)
</div><div>
T=0.0286
(128/4480, Estonian)
</div><div>
T=0.0423
(163/3854, ALSPAC)
</div><div>
T=0.0369
(137/3708, TWINSUK)
</div><div>
T=0.0294
(97/3300, PRJNA289433)
</div><div>
T=0.0205
(60/2922, KOREAN)
</div><div>
T=0.0197
(36/1832, Korea1K)
</div><div>
T=0.043
(43/998, GoNL)
</div><div>
T=0.028
(17/614, Vietnamese)
</div><div>
T=0.030
(18/600, NorthernSweden)
</div><div>
T=0.064
(34/534, MGP)
</div><div>
T=0.026
(8/304, FINRISK)
</div><div>
T=0.111
(24/216, Qatari)
</div><div>
C=0.46
(24/52, SGDP_PRJ)
</div><div>
T=0.07
(3/40, GENOME_DK)
</div><div>
C=0.5
(1/2, Siberian)
</div><div>
T=0.5
(1/2, Siberian)
</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=((105957[AlleleID]))">ClinVar</a>
</dd>
<dt>Gene : Consequence</dt>
<dd>
<div>DPYD : Missense Variant</div><span>DPYD-AS1 : Intron Variant</span>
</dd>
<dt>Publications</dt>
<dd>
<a id="snp_pub_count" href="#publications">26
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>
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<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>
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<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>
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<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>
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<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
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class="js-tablist__link">History
<span aria-hidden="true"></span></a>
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<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>
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data-ga-action="Click-on-horizontal" data-ga-label="Flanks" id="label_id_eighth"
class="js-tablist__link">Flanks
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<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">239272</td>
<td class="popfreq_ref_allele">C=0.949877</td>
<td class="popfreq_alt_allele">T=0.050123</td>
<td class="popfreq_alt_allele">0.902722</td>
<td class="popfreq_alt_allele">0.002967</td>
<td class="popfreq_alt_allele">0.094311</td>
<td class="popfreq_alt_allele">6</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492695">European</a>
</td>
<td>Sub</td>
<td class="samp_s">202338</td>
<td class="popfreq_ref_allele">C=0.948808</td>
<td class="popfreq_alt_allele">T=0.051192</td>
<td class="popfreq_alt_allele">0.900503</td>
<td class="popfreq_alt_allele">0.002886</td>
<td class="popfreq_alt_allele">0.096611</td>
<td class="popfreq_alt_allele">2</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492703">African</a>
</td>
<td>Sub</td>
<td class="samp_s">9830</td>
<td class="popfreq_ref_allele">C=0.9722</td>
<td class="popfreq_alt_allele">T=0.0278</td>
<td class="popfreq_alt_allele">0.94588</td>
<td class="popfreq_alt_allele">0.001424</td>
<td class="popfreq_alt_allele">0.052696</td>
<td class="popfreq_alt_allele">2</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492696">African Others</a>
</td>
<td>Sub</td>
<td class="samp_s">360</td>
<td class="popfreq_ref_allele">C=0.986</td>
<td class="popfreq_alt_allele">T=0.014</td>
<td class="popfreq_alt_allele">0.972222</td>
<td class="popfreq_alt_allele">0.0</td>
<td class="popfreq_alt_allele">0.027778</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492698">African American</a>
</td>
<td>Sub</td>
<td class="samp_s">9470</td>
<td class="popfreq_ref_allele">C=0.9717</td>
<td class="popfreq_alt_allele">T=0.0283</td>
<td class="popfreq_alt_allele">0.944879</td>
<td class="popfreq_alt_allele">0.001478</td>
<td class="popfreq_alt_allele">0.053643</td>
<td class="popfreq_alt_allele">2</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492704">Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">6398</td>
<td class="popfreq_ref_allele">C=0.9737</td>
<td class="popfreq_alt_allele">T=0.0263</td>
<td class="popfreq_alt_allele">0.949359</td>
<td class="popfreq_alt_allele">0.001876</td>
<td class="popfreq_alt_allele">0.048765</td>
<td class="popfreq_alt_allele">4</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492697">East Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">4548</td>
<td class="popfreq_ref_allele">C=0.9837</td>
<td class="popfreq_alt_allele">T=0.0163</td>
<td class="popfreq_alt_allele">0.968338</td>
<td class="popfreq_alt_allele">0.00088</td>
<td class="popfreq_alt_allele">0.030783</td>
<td class="popfreq_alt_allele">2</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492701">Other Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">1850</td>
<td class="popfreq_ref_allele">C=0.9492</td>
<td class="popfreq_alt_allele">T=0.0508</td>
<td class="popfreq_alt_allele">0.902703</td>
<td class="popfreq_alt_allele">0.004324</td>
<td class="popfreq_alt_allele">0.092973</td>
<td class="popfreq_alt_allele">1</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492699">Latin American 1</a>
</td>
<td>Sub</td>
<td class="samp_s">804</td>
<td class="popfreq_ref_allele">C=0.935</td>
<td class="popfreq_alt_allele">T=0.065</td>
<td class="popfreq_alt_allele">0.873134</td>
<td class="popfreq_alt_allele">0.002488</td>
<td class="popfreq_alt_allele">0.124378</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492700">Latin American 2</a>
</td>
<td>Sub</td>
<td class="samp_s">974</td>
<td class="popfreq_ref_allele">C=0.964</td>
<td class="popfreq_alt_allele">T=0.036</td>
<td class="popfreq_alt_allele">0.930185</td>
<td class="popfreq_alt_allele">0.002053</td>
<td class="popfreq_alt_allele">0.067762</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN10492702">South Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">280</td>
<td class="popfreq_ref_allele">C=0.911</td>
<td class="popfreq_alt_allele">T=0.089</td>
<td class="popfreq_alt_allele">0.828571</td>
<td class="popfreq_alt_allele">0.007143</td>
<td class="popfreq_alt_allele">0.164286</td>
<td class="popfreq_alt_allele">0</td>
</tr>
<tr class="chi_row">
<td>
<a href="/biosample/SAMN11605645">Other</a>
</td>
<td>Sub</td>
<td class="samp_s">18648</td>
<td class="popfreq_ref_allele">C=0.94198</td>
<td class="popfreq_alt_allele">T=0.05802</td>
<td class="popfreq_alt_allele">0.888996</td>
<td class="popfreq_alt_allele">0.005041</td>
<td class="popfreq_alt_allele">0.105963</td>
<td class="popfreq_alt_allele">5</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/rs1801160/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/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
Global
</td>
<td>Study-wide</td>
<td class="samp_s">1399990</td>
<td>C=0.9529025</td>
<td>T=0.0470975</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
European
</td>
<td>Sub</td>
<td class="samp_s">1164274</td>
<td>C=0.9559975</td>
<td>T=0.0440025</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
South Asian
</td>
<td>Sub</td>
<td class="samp_s">86246</td>
<td>C=0.90357</td>
<td>T=0.09643</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
American
</td>
<td>Sub</td>
<td class="samp_s">44638</td>
<td>C=0.97213</td>
<td>T=0.02787</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
East Asian
</td>
<td>Sub</td>
<td class="samp_s">39652</td>
<td>C=0.98096</td>
<td>T=0.01904</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
African
</td>
<td>Sub</td>
<td class="samp_s">33378</td>
<td>C=0.97441</td>
<td>T=0.02559</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
Ashkenazi Jewish
</td>
<td>Sub</td>
<td class="samp_s">26052</td>
<td>C=0.89199</td>
<td>T=0.10801</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Exomes</a>
</td>
<td>
Middle Eastern
</td>
<td>sub</td>
<td class="samp_s">5750</td>
<td>C=0.8746</td>
<td>T=0.1254</td>
</tr>
<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>C=0.959330</td>
<td>T=0.040670</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">239272</td>
<td>C=0.949877</td>
<td>T=0.050123</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">202338</td>
<td>C=0.948808</td>
<td>T=0.051192</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">18648</td>
<td>C=0.94198</td>
<td>T=0.05802</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">9830</td>
<td>C=0.9722</td>
<td>T=0.0278</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">6398</td>
<td>C=0.9737</td>
<td>T=0.0263</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">974</td>
<td>C=0.964</td>
<td>T=0.036</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">804</td>
<td>C=0.935</td>
<td>T=0.065</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">280</td>
<td>C=0.911</td>
<td>T=0.089</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
Global
</td>
<td>Study-wide</td>
<td class="samp_s">148940</td>
<td>C=0.960071</td>
<td>T=0.039929</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
European
</td>
<td>Sub</td>
<td class="samp_s">78502</td>
<td>C=0.95791</td>
<td>T=0.04209</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
African
</td>
<td>Sub</td>
<td class="samp_s">41518</td>
<td>C=0.97550</td>
<td>T=0.02450</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
American
</td>
<td>Sub</td>
<td class="samp_s">15224</td>
<td>C=0.95409</td>
<td>T=0.04591</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
East Asian
</td>
<td>Sub</td>
<td class="samp_s">5132</td>
<td>C=0.9846</td>
<td>T=0.0154</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
South Asian
</td>
<td>Sub</td>
<td class="samp_s">4806</td>
<td>C=0.9070</td>
<td>T=0.0930</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
Ashkenazi Jewish
</td>
<td>Sub</td>
<td class="samp_s">3464</td>
<td>C=0.8932</td>
<td>T=0.1068</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA398795">gnomAD v4 - Genomes</a>
</td>
<td>
Middle Eastern
</td>
<td>sub</td>
<td class="samp_s">294</td>
<td>C=0.895</td>
<td>T=0.105</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
<a href="/biosample/SAMN07490465">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">121146</td>
<td>C=0.953527</td>
<td>T=0.046473</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
Europe
</td>
<td>Sub</td>
<td class="samp_s">73292</td>
<td>C=0.95534</td>
<td>T=0.04466</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
Asian
</td>
<td>Sub</td>
<td class="samp_s">25092</td>
<td>C=0.93034</td>
<td>T=0.06966</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
American
</td>
<td>Sub</td>
<td class="samp_s">11452</td>
<td>C=0.97590</td>
<td>T=0.02410</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
African
</td>
<td>Sub</td>
<td class="samp_s">10404</td>
<td>C=0.97443</td>
<td>T=0.02557</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB8661">ExAC</a>
</td>
<td>
<a href="/biosample/SAMN07486028">Other</a>
</td>
<td>Sub</td>
<td class="samp_s">906</td>
<td>C=0.926</td>
<td>T=0.074</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868975">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">78702</td>
<td>C=0.96501</td>
<td>T=0.03499</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868721">AfricanAmerican</a>
</td>
<td>Sub</td>
<td class="samp_s">32516</td>
<td>C=0.97352</td>
<td>T=0.02648</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868735">Mexican</a>
</td>
<td>Sub</td>
<td class="samp_s">10810</td>
<td>C=0.97160</td>
<td>T=0.02840</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868722">Asian</a>
</td>
<td>Sub</td>
<td class="samp_s">8318</td>
<td>C=0.9792</td>
<td>T=0.0208</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868968">PuertoRican</a>
</td>
<td>Sub</td>
<td class="samp_s">7918</td>
<td>C=0.9302</td>
<td>T=0.0698</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868777">NativeHawaiian</a>
</td>
<td>Sub</td>
<td class="samp_s">4534</td>
<td>C=0.9532</td>
<td>T=0.0468</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868733">Cuban</a>
</td>
<td>Sub</td>
<td class="samp_s">4230</td>
<td>C=0.9414</td>
<td>T=0.0586</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868734">Dominican</a>
</td>
<td>Sub</td>
<td class="samp_s">3828</td>
<td>C=0.9616</td>
<td>T=0.0384</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868729">CentralAmerican</a>
</td>
<td>Sub</td>
<td class="samp_s">2450</td>
<td>C=0.9727</td>
<td>T=0.0273</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868969">SouthAmerican</a>
</td>
<td>Sub</td>
<td class="samp_s">1982</td>
<td>C=0.9642</td>
<td>T=0.0358</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868739">NativeAmerican</a>
</td>
<td>Sub</td>
<td class="samp_s">1260</td>
<td>C=0.9746</td>
<td>T=0.0254</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJNA168052">The PAGE Study</a>
</td>
<td>
<a href="/biosample/SAMN10868970">SouthAsian</a>
</td>
<td>Sub</td>
<td class="samp_s">856</td>
<td>C=0.903</td>
<td>T=0.097</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA678214">38KJPN</a>
</td>
<td>
<a href="/biosample/SAMN33574975">JAPANESE</a>
</td>
<td>Study-wide</td>
<td class="samp_s">77428</td>
<td>C=0.98290</td>
<td>T=0.01710</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">13006</td>
<td>C=0.95863</td>
<td>T=0.04137</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">8600</td>
<td>C=0.9533</td>
<td>T=0.0467</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">4406</td>
<td>C=0.9691</td>
<td>T=0.0309</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA974196">Korean Genome Project 4K</a>
</td>
<td>
KOREAN
</td>
<td>Study-wide</td>
<td class="samp_s">7232</td>
<td>C=0.9800</td>
<td>T=0.0200</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>C=0.9567</td>
<td>T=0.0433</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>C=0.9765</td>
<td>T=0.0235</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>C=0.9494</td>
<td>T=0.0506</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>C=0.9151</td>
<td>T=0.0849</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>C=0.9821</td>
<td>T=0.0179</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>C=0.951</td>
<td>T=0.049</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>C=0.9561</td>
<td>T=0.0439</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>C=0.9758</td>
<td>T=0.0242</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>C=0.9851</td>
<td>T=0.0149</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>C=0.9503</td>
<td>T=0.0497</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>C=0.913</td>
<td>T=0.087</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>C=0.945</td>
<td>T=0.055</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA489787">Genetic variation in the Estonian population</a>
</td>
<td>
Estonian
</td>
<td>Study-wide</td>
<td class="samp_s">4480</td>
<td>C=0.9714</td>
<td>T=0.0286</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB7217">The Avon Longitudinal Study of Parents and Children</a>
</td>
<td>
PARENT AND CHILD COHORT
</td>
<td>Study-wide</td>
<td class="samp_s">3854</td>
<td>C=0.9577</td>
<td>T=0.0423</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB7218">UK 10K study - Twins</a>
</td>
<td>
TWIN COHORT
</td>
<td>Study-wide</td>
<td class="samp_s">3708</td>
<td>C=0.9631</td>
<td>T=0.0369</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB37766">MxGDAR/Encodat-PGx</a>
</td>
<td>
<a href="/biosample/SAMN15457995">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">3300</td>
<td>C=0.9706</td>
<td>T=0.0294</td>
</tr>
<tr class="chi_row">
<td>
<a href="/bioproject/PRJEB37766">MxGDAR/Encodat-PGx</a>
</td>
<td>
MxGDAR
</td>
<td>Sub</td>
<td class="samp_s">3300</td>
<td>C=0.9706</td>
<td>T=0.0294</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA589833">KOREAN population from KRGDB</a>
</td>
<td>
KOREAN
</td>
<td>Study-wide</td>
<td class="samp_s">2922</td>
<td>C=0.9795</td>
<td>T=0.0205</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA609628">Korean Genome Project</a>
</td>
<td>
KOREAN
</td>
<td>Study-wide</td>
<td class="samp_s">1832</td>
<td>C=0.9803</td>
<td>T=0.0197</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB5829">Genome of the Netherlands Release 5</a>
</td>
<td>
<a href="/biosample/SAMN13000132">Genome of the Netherlands</a>
</td>
<td>Study-wide</td>
<td class="samp_s">998</td>
<td>C=0.957</td>
<td>T=0.043</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA515199">A Vietnamese Genetic Variation Database</a>
</td>
<td>
<a href="/biosample/SAMN10744005">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">614</td>
<td>C=0.972</td>
<td>T=0.028</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PPRJNA503394">Northern Sweden</a>
</td>
<td>
<a href="/biosample/SAMN10359154">ACPOP</a>
</td>
<td>Study-wide</td>
<td class="samp_s">600</td>
<td>C=0.970</td>
<td>T=0.030</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB8705">Medical Genome Project healthy controls from Spanish population</a>
</td>
<td>
<a href="/biosample/SAMN13001620">Spanish controls</a>
</td>
<td>Study-wide</td>
<td class="samp_s">534</td>
<td>C=0.936</td>
<td>T=0.064</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB7895">FINRISK</a>
</td>
<td>
<a href="/biosample/SAMN13002954">Finnish from FINRISK project</a>
</td>
<td>Study-wide</td>
<td class="samp_s">304</td>
<td>C=0.974</td>
<td>T=0.026</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA288297">Qatari</a>
</td>
<td>
<a href="/biosample/SAMN13019808">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">216</td>
<td>C=0.889</td>
<td>T=0.111</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">52</td>
<td>C=0.46</td>
<td>T=0.54</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJEB7725">The Danish reference pan genome</a>
</td>
<td>
<a href="/biosample/SAMN13003120">Danish</a>
</td>
<td>Study-wide</td>
<td class="samp_s">40</td>
<td>C=0.93</td>
<td>T=0.07</td>
</tr>
<tr class="par_row">
<td>
<a href="/bioproject/PRJNA267856">Siberian</a>
</td>
<td>
<a href="/biosample/SAMN13113809">Global</a>
</td>
<td>Study-wide</td>
<td class="samp_s">2</td>
<td>C=0.5</td>
<td>T=0.5</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 1</td>
<td>NC_000001.11:g.97305364C>A</td>
</tr>
<tr>
<td>GRCh38.p14 chr 1</td>
<td>NC_000001.11:g.97305364C>G</td>
</tr>
<tr>
<td>GRCh38.p14 chr 1</td>
<td>NC_000001.11:g.97305364C>T</td>
</tr>
<tr>
<td>GRCh37.p13 chr 1</td>
<td>NC_000001.10:g.97770920C>A</td>
</tr>
<tr>
<td>GRCh37.p13 chr 1</td>
<td>NC_000001.10:g.97770920C>G</td>
</tr>
<tr>
<td>GRCh37.p13 chr 1</td>
<td>NC_000001.10:g.97770920C>T</td>
</tr>
<tr>
<td>DPYD RefSeqGene (LRG_722)</td>
<td>NG_008807.2:g.620696G>T</td>
</tr>
<tr>
<td>DPYD RefSeqGene (LRG_722)</td>
<td>NG_008807.2:g.620696G>C</td>
</tr>
<tr>
<td>DPYD RefSeqGene (LRG_722)</td>
<td>NG_008807.2:g.620696G>A</td>
</tr>
</tbody>
</table>
</div>
<div id="trans_anno_allele">
<div class="sect_heading">
Gene: <a target="_blank" data-section="Variant Details"
data-ga-action="Click-on"
data-ga-label="transcript_annotation_gene_link"
ref="section=Variant Details&action=Click-on&label=transcript_annotation_gene_link"
href="/gene/1806">DPYD</a>, dihydropyrimidine dehydrogenase
(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>DPYD transcript variant 2</td>
<td>
<span>
NM_001160301.1:c.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant 1</td>
<td>
<span>
NM_000110.4:c.2194G>T
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > F [</span><span class="codon-hilite">T</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform 1</td>
<td>
<span>
NP_000101.2:p.Val732Phe
</span>
</td>
<td>
<span>
V (Val) > F (Phe)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_odd">
<td>DPYD transcript variant 1</td>
<td>
<span>
NM_000110.4:c.2194G>C
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > L [</span><span class="codon-hilite">C</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform 1</td>
<td>
<span>
NP_000101.2:p.Val732Leu
</span>
</td>
<td>
<span>
V (Val) > L (Leu)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant 1</td>
<td>
<span>
NM_000110.4:c.2194G>A
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > I [</span><span class="codon-hilite">A</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform 1</td>
<td>
<span>
NP_000101.2:p.Val732Ile
</span>
</td>
<td>
<span>
V (Val) > I (Ile)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_odd">
<td>DPYD transcript variant X2</td>
<td>
<span>
XM_005270562.3:c.1978G>T
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > F [</span><span class="codon-hilite">T</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X2</td>
<td>
<span>
XP_005270619.2:p.Val660Phe
</span>
</td>
<td>
<span>
V (Val) > F (Phe)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant X2</td>
<td>
<span>
XM_005270562.3:c.1978G>C
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > L [</span><span class="codon-hilite">C</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X2</td>
<td>
<span>
XP_005270619.2:p.Val660Leu
</span>
</td>
<td>
<span>
V (Val) > L (Leu)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_odd">
<td>DPYD transcript variant X2</td>
<td>
<span>
XM_005270562.3:c.1978G>A
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > I [</span><span class="codon-hilite">A</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X2</td>
<td>
<span>
XP_005270619.2:p.Val660Ile
</span>
</td>
<td>
<span>
V (Val) > I (Ile)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant X1</td>
<td>
<span>
XM_017000507.2:c.2083G>T
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > F [</span><span class="codon-hilite">T</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X1</td>
<td>
<span>
XP_016855996.1:p.Val695Phe
</span>
</td>
<td>
<span>
V (Val) > F (Phe)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_odd">
<td>DPYD transcript variant X1</td>
<td>
<span>
XM_017000507.2:c.2083G>C
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > L [</span><span class="codon-hilite">C</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X1</td>
<td>
<span>
XP_016855996.1:p.Val695Leu
</span>
</td>
<td>
<span>
V (Val) > L (Leu)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant X1</td>
<td>
<span>
XM_017000507.2:c.2083G>A
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > I [</span><span class="codon-hilite">A</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X1</td>
<td>
<span>
XP_016855996.1:p.Val695Ile
</span>
</td>
<td>
<span>
V (Val) > I (Ile)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_odd">
<td>DPYD transcript variant X3</td>
<td>
<span>
XM_047448076.1:c.1966G>T
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > F [</span><span class="codon-hilite">T</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X3</td>
<td>
<span>
XP_047304032.1:p.Val656Phe
</span>
</td>
<td>
<span>
V (Val) > F (Phe)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant X3</td>
<td>
<span>
XM_047448076.1:c.1966G>C
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > L [</span><span class="codon-hilite">C</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X3</td>
<td>
<span>
XP_047304032.1:p.Val656Leu
</span>
</td>
<td>
<span>
V (Val) > L (Leu)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_odd">
<td>DPYD transcript variant X3</td>
<td>
<span>
XM_047448076.1:c.1966G>A
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > I [</span><span class="codon-hilite">A</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X3</td>
<td>
<span>
XP_047304032.1:p.Val656Ile
</span>
</td>
<td>
<span>
V (Val) > I (Ile)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant X4</td>
<td>
<span>
XM_047448077.1:c.1867G>T
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > F [</span><span class="codon-hilite">T</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X4</td>
<td>
<span>
XP_047304033.1:p.Val623Phe
</span>
</td>
<td>
<span>
V (Val) > F (Phe)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_odd">
<td>DPYD transcript variant X4</td>
<td>
<span>
XM_047448077.1:c.1867G>C
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > L [</span><span class="codon-hilite">C</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X4</td>
<td>
<span>
XP_047304033.1:p.Val623Leu
</span>
</td>
<td>
<span>
V (Val) > L (Leu)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant X4</td>
<td>
<span>
XM_047448077.1:c.1867G>A
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > I [</span><span class="codon-hilite">A</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X4</td>
<td>
<span>
XP_047304033.1:p.Val623Ile
</span>
</td>
<td>
<span>
V (Val) > I (Ile)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_odd">
<td>DPYD transcript variant X5</td>
<td>
<span>
XM_006710397.4:c.2194G>T
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > F [</span><span class="codon-hilite">T</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X5</td>
<td>
<span>
XP_006710460.1:p.Val732Phe
</span>
</td>
<td>
<span>
V (Val) > F (Phe)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant X5</td>
<td>
<span>
XM_006710397.4:c.2194G>C
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > L [</span><span class="codon-hilite">C</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_even">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X5</td>
<td>
<span>
XP_006710460.1:p.Val732Leu
</span>
</td>
<td>
<span>
V (Val) > L (Leu)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_odd">
<td>DPYD transcript variant X5</td>
<td>
<span>
XM_006710397.4:c.2194G>A
</span>
</td>
<td>
<span><span class="codon-plain">V [</span><span class="codon-hilite">G</span><span class="codon-ghost">TT</span><span class="codon-plain">] > I [</span><span class="codon-hilite">A</span><span class="codon-ghost">TT</span><span class="codon-plain">]</span></span>
</td>
<td>
Coding Sequence Variant
</td>
</tr>
<tr class="vard_odd">
<td>dihydropyrimidine dehydrogenase [NADP(+)] isoform X5</td>
<td>
<span>
XP_006710460.1:p.Val732Ile
</span>
</td>
<td>
<span>
V (Val) > I (Ile)
</span>
</td>
<td>
Missense Variant
</td>
</tr>
<tr class="vard_even">
<td>DPYD transcript variant X6</td>
<td>
<span>
XR_001737014.2:n.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Genic Downstream Transcript Variant
</td>
</tr>
</tbody>
</table>
<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/100873932">DPYD-AS1</a>, DPYD antisense RNA 1
(plus 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>DPYD-AS1 transcript</td>
<td>
<span>
NR_046590.1:n.
</span>
</td>
<td>
<span>
N/A
</span>
</td>
<td>
Intron 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: T (allele ID:
<a ref="section=Clinical Significance&action=Click-on&label=allele_link"
target="_blank" href="/clinvar?term=(105957[AlleleID])"
data-section="Clinical Significance"
data-ga-action="Click-on"
data-ga-label="allele_link">
105957
</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/RCV000086462.9">RCV000086462.9</a>
</td>
<td>not provided</td>
<td>Benign</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000249656.10">RCV000249656.10</a>
</td>
<td>not specified</td>
<td>Benign</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV000407597.5">RCV000407597.5</a>
</td>
<td>Dihydropyrimidine dehydrogenase deficiency</td>
<td>Likely-Benign</td>
</tr>
<tr>
<td><a target="_blank" data-section="Clinical Significance"
data-ga-action="Click-on" data-ga-label="ClinVar_Accession_link"
ref="section=Clinical Significance&action=Click-on&label=ClinVar_Accession_link"
href="/clinvar/RCV001787902.1">RCV001787902.1</a>
</td>
<td>fluorouracil response - Other</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/RCV001787903.2">RCV001787903.2</a>
</td>
<td>capecitabine response - Toxicity</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/RCV001787904.2">RCV001787904.2</a>
</td>
<td>fluorouracil response - Toxicity</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/RCV003891585.1">RCV003891585.1</a>
</td>
<td>DPYD-related disorder</td>
<td>Likely-Benign</td>
</tr>
</tbody>
</table>
</div>
</div>
<div id="hgvs_tab" class="js-tabcontent">
<a data-width="640px" href="#aliases_tp"
ref="section=HGVS&action=Click-on-Tooltip&label=aliases_tp"
data-section="HGVS" data-ga-action="Click-on-Tooltip" data-ga-label="aliases_tp"
class="fa fa-question-circle align-right ncbiPopper">
<span class="usa-sr-only">Help</span>
</a>
<p id="aliases_tp">
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. <a href="http://varnomen.hgvs.org/">HGVS name</a> is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".</p>
<div id="hgvs">
<table id="alliases_alleles_datatable" class="stripe">
<thead class="allele_wrap">
<tr>
<th>Placement</th>
<th>
C=
</th>
<th>
A
</th>
<th>
G
</th>
<th>
T
</th>
</tr>
</thead>
<tbody class="allele_wrap">
<tr>
<td class="alias_hgvs">
GRCh38.p14 chr 1
</td>
<td class="alias_hgvs">
NC_000001.11:g.97305364=
</td>
<td class="alias_hgvs">
NC_000001.11:g.97305364C>A
</td>
<td class="alias_hgvs">
NC_000001.11:g.97305364C>G
</td>
<td class="alias_hgvs">
NC_000001.11:g.97305364C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
GRCh37.p13 chr 1
</td>
<td class="alias_hgvs">
NC_000001.10:g.97770920=
</td>
<td class="alias_hgvs">
NC_000001.10:g.97770920C>A
</td>
<td class="alias_hgvs">
NC_000001.10:g.97770920C>G
</td>
<td class="alias_hgvs">
NC_000001.10:g.97770920C>T
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD RefSeqGene (LRG_722)
</td>
<td class="alias_hgvs">
NG_008807.2:g.620696=
</td>
<td class="alias_hgvs">
NG_008807.2:g.620696G>T
</td>
<td class="alias_hgvs">
NG_008807.2:g.620696G>C
</td>
<td class="alias_hgvs">
NG_008807.2:g.620696G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant 1
</td>
<td class="alias_hgvs">
NM_000110.4:c.2194=
</td>
<td class="alias_hgvs">
NM_000110.4:c.2194G>T
</td>
<td class="alias_hgvs">
NM_000110.4:c.2194G>C
</td>
<td class="alias_hgvs">
NM_000110.4:c.2194G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant 1
</td>
<td class="alias_hgvs">
NM_000110.3:c.2194=
</td>
<td class="alias_hgvs">
NM_000110.3:c.2194G>T
</td>
<td class="alias_hgvs">
NM_000110.3:c.2194G>C
</td>
<td class="alias_hgvs">
NM_000110.3:c.2194G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X5
</td>
<td class="alias_hgvs">
XM_006710397.4:c.2194=
</td>
<td class="alias_hgvs">
XM_006710397.4:c.2194G>T
</td>
<td class="alias_hgvs">
XM_006710397.4:c.2194G>C
</td>
<td class="alias_hgvs">
XM_006710397.4:c.2194G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X3
</td>
<td class="alias_hgvs">
XM_006710397.3:c.2194=
</td>
<td class="alias_hgvs">
XM_006710397.3:c.2194G>T
</td>
<td class="alias_hgvs">
XM_006710397.3:c.2194G>C
</td>
<td class="alias_hgvs">
XM_006710397.3:c.2194G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X2
</td>
<td class="alias_hgvs">
XM_006710397.2:c.2194=
</td>
<td class="alias_hgvs">
XM_006710397.2:c.2194G>T
</td>
<td class="alias_hgvs">
XM_006710397.2:c.2194G>C
</td>
<td class="alias_hgvs">
XM_006710397.2:c.2194G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X3
</td>
<td class="alias_hgvs">
XM_006710397.1:c.2194=
</td>
<td class="alias_hgvs">
XM_006710397.1:c.2194G>T
</td>
<td class="alias_hgvs">
XM_006710397.1:c.2194G>C
</td>
<td class="alias_hgvs">
XM_006710397.1:c.2194G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X2
</td>
<td class="alias_hgvs">
XM_005270562.3:c.1978=
</td>
<td class="alias_hgvs">
XM_005270562.3:c.1978G>T
</td>
<td class="alias_hgvs">
XM_005270562.3:c.1978G>C
</td>
<td class="alias_hgvs">
XM_005270562.3:c.1978G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X2
</td>
<td class="alias_hgvs">
XM_005270562.2:c.1978=
</td>
<td class="alias_hgvs">
XM_005270562.2:c.1978G>T
</td>
<td class="alias_hgvs">
XM_005270562.2:c.1978G>C
</td>
<td class="alias_hgvs">
XM_005270562.2:c.1978G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X2
</td>
<td class="alias_hgvs">
XM_005270562.1:c.1978=
</td>
<td class="alias_hgvs">
XM_005270562.1:c.1978G>T
</td>
<td class="alias_hgvs">
XM_005270562.1:c.1978G>C
</td>
<td class="alias_hgvs">
XM_005270562.1:c.1978G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X1
</td>
<td class="alias_hgvs">
XM_017000507.2:c.2083=
</td>
<td class="alias_hgvs">
XM_017000507.2:c.2083G>T
</td>
<td class="alias_hgvs">
XM_017000507.2:c.2083G>C
</td>
<td class="alias_hgvs">
XM_017000507.2:c.2083G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X1
</td>
<td class="alias_hgvs">
XM_017000507.1:c.2083=
</td>
<td class="alias_hgvs">
XM_017000507.1:c.2083G>T
</td>
<td class="alias_hgvs">
XM_017000507.1:c.2083G>C
</td>
<td class="alias_hgvs">
XM_017000507.1:c.2083G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X3
</td>
<td class="alias_hgvs">
XM_047448076.1:c.1966=
</td>
<td class="alias_hgvs">
XM_047448076.1:c.1966G>T
</td>
<td class="alias_hgvs">
XM_047448076.1:c.1966G>C
</td>
<td class="alias_hgvs">
XM_047448076.1:c.1966G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
DPYD transcript variant X4
</td>
<td class="alias_hgvs">
XM_047448077.1:c.1867=
</td>
<td class="alias_hgvs">
XM_047448077.1:c.1867G>T
</td>
<td class="alias_hgvs">
XM_047448077.1:c.1867G>C
</td>
<td class="alias_hgvs">
XM_047448077.1:c.1867G>A
</td>
</tr>
<tr>
<td class="alias_hgvs">
dihydropyrimidine dehydrogenase [NADP(+)] isoform 1
</td>
<td class="alias_hgvs">
NP_000101.2:p.Val732=
</td>
<td class="alias_hgvs">
NP_000101.2:p.Val732Phe
</td>
<td class="alias_hgvs">
NP_000101.2:p.Val732Leu
</td>
<td class="alias_hgvs">
NP_000101.2:p.Val732Ile
</td>
</tr>
<tr>
<td class="alias_hgvs">
dihydropyrimidine dehydrogenase [NADP(+)] isoform X5
</td>
<td class="alias_hgvs">
XP_006710460.1:p.Val732=
</td>
<td class="alias_hgvs">
XP_006710460.1:p.Val732Phe
</td>
<td class="alias_hgvs">
XP_006710460.1:p.Val732Leu
</td>
<td class="alias_hgvs">
XP_006710460.1:p.Val732Ile
</td>
</tr>
<tr>
<td class="alias_hgvs">
dihydropyrimidine dehydrogenase [NADP(+)] isoform X2
</td>
<td class="alias_hgvs">
XP_005270619.2:p.Val660=
</td>
<td class="alias_hgvs">
XP_005270619.2:p.Val660Phe
</td>
<td class="alias_hgvs">
XP_005270619.2:p.Val660Leu
</td>
<td class="alias_hgvs">
XP_005270619.2:p.Val660Ile
</td>
</tr>
<tr>
<td class="alias_hgvs">
dihydropyrimidine dehydrogenase [NADP(+)] isoform X1
</td>
<td class="alias_hgvs">
XP_016855996.1:p.Val695=
</td>
<td class="alias_hgvs">
XP_016855996.1:p.Val695Phe
</td>
<td class="alias_hgvs">
XP_016855996.1:p.Val695Leu
</td>
<td class="alias_hgvs">
XP_016855996.1:p.Val695Ile
</td>
</tr>
<tr>
<td class="alias_hgvs">
dihydropyrimidine dehydrogenase [NADP(+)] isoform X3
</td>
<td class="alias_hgvs">
XP_047304032.1:p.Val656=
</td>
<td class="alias_hgvs">
XP_047304032.1:p.Val656Phe
</td>
<td class="alias_hgvs">
XP_047304032.1:p.Val656Leu
</td>
<td class="alias_hgvs">
XP_047304032.1:p.Val656Ile
</td>
</tr>
<tr>
<td class="alias_hgvs">
dihydropyrimidine dehydrogenase [NADP(+)] isoform X4
</td>
<td class="alias_hgvs">
XP_047304033.1:p.Val623=
</td>
<td class="alias_hgvs">
XP_047304033.1:p.Val623Phe
</td>
<td class="alias_hgvs">
XP_047304033.1:p.Val623Leu
</td>
<td class="alias_hgvs">
XP_047304033.1:p.Val623Ile
</td>
</tr>
<tr>
<td class="alias_hgvs">
dihydropyrimidine dehydrogenase [NADP(+)] isoform X2
</td>
<td class="alias_hgvs">
XP_005270619.1:p.Val660=
</td>
<td class="alias_hgvs">
XP_005270619.1:p.Val660Phe
</td>
<td class="alias_hgvs">
XP_005270619.1:p.Val660Leu
</td>
<td class="alias_hgvs">
XP_005270619.1:p.Val660Ile
</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">
123 SubSNP,
26 Frequency,
7 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>
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=ss86237232">ss86237232</a>
</td>
<td>Mar 23, 2008
(129)
</td>
</tr>
<tr >
<td>2</td>
<td>
CANCER-GENOME
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss86342029">ss86342029</a>
</td>
<td>Mar 23, 2008
(129)
</td>
</tr>
<tr >
<td>3</td>
<td>
SEATTLESEQ
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss159698104">ss159698104</a>
</td>
<td>Dec 01, 2009
(131)
</td>
</tr>
<tr >
<td>4</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=ss230650502">ss230650502</a>
</td>
<td>Jul 14, 2010
(132)
</td>
</tr>
<tr >
<td>5</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=ss341976617">ss341976617</a>
</td>
<td>May 09, 2011
(134)
</td>
</tr>
<tr >
<td>6</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=ss489753540">ss489753540</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>7</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=ss491297106">ss491297106</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>8</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=ss491598669">ss491598669</a>
</td>
<td>May 04, 2012
(137)
</td>
</tr>
<tr >
<td>9</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=ss536447695">ss536447695</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>10</td>
<td>
SSMP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss648243125">ss648243125</a>
</td>
<td>Apr 25, 2013
(138)
</td>
</tr>
<tr >
<td>11</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=ss780879233">ss780879233</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>12</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=ss783564825">ss783564825</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>13</td>
<td>
EVA-GONL
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss975466004">ss975466004</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>14</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=ss1067423555">ss1067423555</a>
</td>
<td>Aug 21, 2014
(142)
</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=ss1068115573">ss1068115573</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=ss1292044731">ss1292044731</a>
</td>
<td>Aug 21, 2014
(142)
</td>
</tr>
<tr >
<td>17</td>
<td>
DDI
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1425906915">ss1425906915</a>
</td>
<td>Apr 01, 2015
(144)
</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=ss1536213393">ss1536213393</a>
</td>
<td>Dec 17, 2014
(142)
</td>
</tr>
<tr >
<td>19</td>
<td>
EVA_GENOME_DK
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1574258809">ss1574258809</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>20</td>
<td>
EVA_FINRISK
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1584009477">ss1584009477</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>21</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=ss1584843466">ss1584843466</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>22</td>
<td>
EVA_UK10K_ALSPAC
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1600782846">ss1600782846</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>23</td>
<td>
EVA_UK10K_TWINSUK
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1643776879">ss1643776879</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>24</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=ss1685649819">ss1685649819</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>25</td>
<td>
EVA_MGP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss1710913131">ss1710913131</a>
</td>
<td>Apr 01, 2015
(144)
</td>
</tr>
<tr >
<td>26</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=ss1751940883">ss1751940883</a>
</td>
<td>Sep 08, 2015
(146)
</td>
</tr>
<tr >
<td>27</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=ss1917731602">ss1917731602</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>28</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=ss1918666620">ss1918666620</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>29</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=ss1946002568">ss1946002568</a>
</td>
<td>Feb 12, 2016
(147)
</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=ss1946002569">ss1946002569</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>31</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=ss1958295929">ss1958295929</a>
</td>
<td>Feb 12, 2016
(147)
</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=ss1958295930">ss1958295930</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>33</td>
<td>
AMU
</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=ss1966654228">ss1966654228</a>
</td>
<td>Feb 12, 2016
(147)
</td>
</tr>
<tr >
<td>34</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=ss2019854516">ss2019854516</a>
</td>
<td>Sep 14, 2016
(149)
</td>
</tr>
<tr >
<td>35</td>
<td>
USC_VALOUEV
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2147873359">ss2147873359</a>
</td>
<td>Dec 20, 2016
(150)
</td>
</tr>
<tr >
<td>36</td>
<td>
HUMAN_LONGEVITY
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2164894675">ss2164894675</a>
</td>
<td>Dec 20, 2016
(150)
</td>
</tr>
<tr >
<td>37</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2632551621">ss2632551621</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>38</td>
<td>
GRF
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2697800468">ss2697800468</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>39</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=ss2710678011">ss2710678011</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>40</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=ss2731656769">ss2731656769</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>41</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=ss2746378391">ss2746378391</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>42</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=ss2758455540">ss2758455540</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>43</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=ss2984868223">ss2984868223</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>44</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=ss2985519653">ss2985519653</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>45</td>
<td>
SWEGEN
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss2987280518">ss2987280518</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>46</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=ss3021112800">ss3021112800</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>47</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=ss3021112801">ss3021112801</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>48</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=ss3029637186">ss3029637186</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>49</td>
<td>
CSHL
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3343588618">ss3343588618</a>
</td>
<td>Nov 08, 2017
(151)
</td>
</tr>
<tr >
<td>50</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=ss3625545894">ss3625545894</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>51</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3626161795">ss3626161795</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>52</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3626161796">ss3626161796</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>53</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3634338344">ss3634338344</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>54</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3640045704">ss3640045704</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>55</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3644498528">ss3644498528</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>56</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=ss3644498529">ss3644498529</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>57</td>
<td>
BIOINF_KMB_FNS_UNIBA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3645059771">ss3645059771</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>58</td>
<td>
OMUKHERJEE_ADBS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3646233640">ss3646233640</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>59</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3651443426">ss3651443426</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>60</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=ss3651443427">ss3651443427</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>61</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=ss3653640098">ss3653640098</a>
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>62</td>
<td>
EGCUT_WGS
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3655363258">ss3655363258</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>63</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=ss3687336880">ss3687336880</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>64</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3725047203">ss3725047203</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>65</td>
<td>
ACPOP
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3727300088">ss3727300088</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>66</td>
<td>
ILLUMINA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3744050794">ss3744050794</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>67</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=ss3744348627">ss3744348627</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>68</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=ss3744639317">ss3744639317</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>69</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=ss3746555641">ss3746555641</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>70</td>
<td>
PAGE_CC
</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=ss3770827301">ss3770827301</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>71</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=ss3772140556">ss3772140556</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>72</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=ss3799557122">ss3799557122</a>
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>73</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=ss3823633476">ss3823633476</a>
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>74</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=ss3825570030">ss3825570030</a>
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>75</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=ss3826318954">ss3826318954</a>
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>76</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=ss3849446400">ss3849446400</a>
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>77</td>
<td>
KRGDB
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3894520663">ss3894520663</a>
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>78</td>
<td>
KOGIC
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss3945063751">ss3945063751</a>
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>79</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=ss3983938241">ss3983938241</a>
</td>
<td>Apr 25, 2021
(155)
</td>
</tr>
<tr >
<td>80</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=ss3983938242">ss3983938242</a>
</td>
<td>Apr 25, 2021
(155)
</td>
</tr>
<tr >
<td>81</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=ss3984447062">ss3984447062</a>
</td>
<td>Apr 25, 2021
(155)
</td>
</tr>
<tr >
<td>82</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=ss3986128424">ss3986128424</a>
</td>
<td>Apr 25, 2021
(155)
</td>
</tr>
<tr >
<td>83</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=ss4460113679">ss4460113679</a>
</td>
<td>Apr 25, 2021
(155)
</td>
</tr>
<tr >
<td>84</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=ss6208433220">ss6208433220</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>85</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=ss6284038584">ss6284038584</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>86</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=ss6322091869">ss6322091869</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>87</td>
<td>
YEGNASUBRAMANIAN_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=ss6334272856">ss6334272856</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>88</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=ss6349481047">ss6349481047</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>89</td>
<td>
KOGIC
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6351998976">ss6351998976</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>90</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=ss6403965851">ss6403965851</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>91</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=ss6404017275">ss6404017275</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>92</td>
<td>
GNOMAD
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6407778568">ss6407778568</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>93</td>
<td>
GNOMAD
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss6494899143">ss6494899143</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>94</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=ss8145243741">ss8145243741</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>95</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=ss8236871138">ss8236871138</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>96</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=ss8237632433">ss8237632433</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>97</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=ss8243268487">ss8243268487</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>98</td>
<td>
TRAN_CS_UWATERLOO
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8314396336">ss8314396336</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>99</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=ss8314636907">ss8314636907</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>100</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=ss8320571763">ss8320571763</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>101</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=ss8444225829">ss8444225829</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>102</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=ss8512473799">ss8512473799</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>103</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=ss8516079296">ss8516079296</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>104</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=ss8624212839">ss8624212839</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>105</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=ss8626101788">ss8626101788</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>106</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=ss8670383989">ss8670383989</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>107</td>
<td>
YY_MCH
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8800847089">ss8800847089</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>108</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=ss8832350780">ss8832350780</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>109</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=ss8847163548">ss8847163548</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>110</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=ss8847548113">ss8847548113</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>111</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=ss8848265986">ss8848265986</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>112</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=ss8849027752">ss8849027752</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>113</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=ss8909410649">ss8909410649</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>114</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=ss8935518838">ss8935518838</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>115</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=ss8937960491">ss8937960491</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>116</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=ss8979283059">ss8979283059</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>117</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=ss8981422808">ss8981422808</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>118</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=ss8981700512">ss8981700512</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>119</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=ss8981700513">ss8981700513</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>120</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=ss8982017092">ss8982017092</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>121</td>
<td>
LNCC-LABINFO
</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=ss8982072041">ss8982072041</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>122</td>
<td>
EVA
</td>
<td>
<a target="_blank" data-section="Submissions"
data-ga-action="Click-on" data-ga-label="Submission_ID_link"
ref="section=Submissions&action=Click-on&label=Submission_ID_link"
href="/projects/SNP/snp_ss.cgi?subsnp_id=ss8982330779">ss8982330779</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>123</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=ss8989718287">ss8989718287</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>124</td>
<td>
1000Genomes
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>125</td>
<td>
1000Genomes_30X
</td>
<td>
NC_000001.11 - 97305364
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>126</td>
<td>
The Avon Longitudinal Study of Parents and Children
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>127</td>
<td>
Genetic variation in the Estonian population
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>128</td>
<td>
ExAC
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>129</td>
<td>
FINRISK
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>130</td>
<td>
The Danish reference pan genome
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>131</td>
<td>
gnomAD v4 - Exomes
</td>
<td>
NC_000001.11 - 97305364
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>132</td>
<td>
gnomAD v4 - Genomes
</td>
<td>
NC_000001.11 - 97305364
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>133</td>
<td>
GO Exome Sequencing Project
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>134</td>
<td>
Genome of the Netherlands Release 5
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>135</td>
<td>
KOREAN population from KRGDB
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>136</td>
<td>
Korean Genome Project
</td>
<td>
NC_000001.11 - 97305364
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>137</td>
<td>
Korean Genome Project 4K
</td>
<td>
NC_000001.11 - 97305364
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>138</td>
<td>
Medical Genome Project healthy controls from Spanish population
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>139</td>
<td>
Northern Sweden
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>140</td>
<td>
The PAGE Study
</td>
<td>
NC_000001.11 - 97305364
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>141</td>
<td>
MxGDAR/Encodat-PGx
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Apr 25, 2021
(155)
</td>
</tr>
<tr >
<td>142</td>
<td>
Qatari
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>143</td>
<td>
SGDP_PRJ
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>144</td>
<td>
Siberian
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Apr 25, 2020
(154)
</td>
</tr>
<tr >
<td>145</td>
<td>
38KJPN
</td>
<td>
NC_000001.11 - 97305364
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>146</td>
<td>
TopMed
</td>
<td>
NC_000001.11 - 97305364
</td>
<td>Apr 25, 2021
(155)
</td>
</tr>
<tr >
<td>147</td>
<td>
UK 10K study - Twins
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Oct 11, 2018
(152)
</td>
</tr>
<tr >
<td>148</td>
<td>
A Vietnamese Genetic Variation Database
</td>
<td>
NC_000001.10 - 97770920
</td>
<td>Jul 12, 2019
(153)
</td>
</tr>
<tr >
<td>149</td>
<td>
ALFA
</td>
<td>
NC_000001.11 - 97305364
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>150</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/RCV000086462.9/">RCV000086462.9</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>151</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/RCV000249656.10/">RCV000249656.10</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>152</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/RCV000407597.5/">RCV000407597.5</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>153</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/RCV001787902.1/">RCV001787902.1</a>
</td>
<td>Oct 12, 2022
(156)
</td>
</tr>
<tr >
<td>154</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/RCV001787903.2/">RCV001787903.2</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>155</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/RCV001787904.2/">RCV001787904.2</a>
</td>
<td>Nov 02, 2024
(157)
</td>
</tr>
<tr >
<td>156</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/RCV003891585.1/">RCV003891585.1</a>
</td>
<td>Nov 02, 2024
(157)
</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="rs12720467">rs12720467</a>
</td>
<td>Oct 07, 2004
(123)
</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="rs12720468">rs12720468</a>
</td>
<td>Oct 07, 2004
(123)
</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="rs199469554">rs199469554</a>
</td>
<td>Dec 28, 2011
(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>
ss6349481047
</td>
<td>
NC_000001.10:97770919:C:A
</td>
<td>
NC_000001.11:97305363:C:A
</td>
<td>
</td>
</tr>
<tr>
<td>
ss6349481047,
ss8935518838
</td>
<td>
NC_000001.10:97770919:C:G
</td>
<td>
NC_000001.11:97305363:C:G
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
ss491598669,
ss1584843466
</td>
<td>
NC_000001.9:97543507:C:T
</td>
<td>
NC_000001.11:97305363:C:T
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
2806174,
1546730,
1101506,
4855715,
5938,
1622086,
92110,
670423,
1698057,
29883,
584953,
63,
708550,
1463380,
389713,
1546730,
332758,
ss230650502,
ss341976617,
ss489753540,
ss491297106,
ss536447695,
ss648243125,
ss780879233,
ss783564825,
ss975466004,
ss1067423555,
ss1068115573,
ss1292044731,
ss1425906915,
ss1574258809,
ss1584009477,
ss1600782846,
ss1643776879,
ss1685649819,
ss1710913131,
ss1751940883,
ss1917731602,
ss1918666620,
ss1946002568,
ss1946002569,
ss1958295929,
ss1958295930,
ss1966654228,
ss2019854516,
ss2147873359,
ss2632551621,
ss2697800468,
ss2710678011,
ss2731656769,
ss2746378391,
ss2758455540,
ss2984868223,
ss2985519653,
ss2987280518,
ss3021112800,
ss3021112801,
ss3029637186,
ss3343588618,
ss3625545894,
ss3626161795,
ss3626161796,
ss3634338344,
ss3640045704,
ss3644498528,
ss3644498529,
ss3646233640,
ss3651443426,
ss3651443427,
ss3653640098,
ss3655363258,
ss3727300088,
ss3744050794,
ss3744348627,
ss3744639317,
ss3746555641,
ss3772140556,
ss3823633476,
ss3825570030,
ss3826318954,
ss3849446400,
ss3894520663,
ss3983938241,
ss3983938242,
ss3984447062,
ss3986128424,
ss6208433220,
ss6284038584,
ss6322091869,
ss6334272856,
ss6403965851,
ss8145243741,
ss8314636907,
ss8320571763,
ss8512473799,
ss8624212839,
ss8626101788,
ss8832350780,
ss8847163548,
ss8847548113,
ss8848265986,
ss8935518838,
ss8937960491,
ss8979283059,
ss8981422808,
ss8981700512,
ss8981700513,
ss8982330779
</td>
<td>
NC_000001.10:97770919:C:T
</td>
<td>
NC_000001.11:97305363:C:T
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
RCV000086462.9,
RCV000249656.10,
RCV000407597.5,
RCV001787902.1,
RCV001787903.2,
RCV001787904.2,
RCV003891585.1,
3605231,
3076900,
21213776,
1441752,
1850874,
48770,
7094107,
23720014,
7209739266,
ss1536213393,
ss2164894675,
ss3645059771,
ss3687336880,
ss3725047203,
ss3770827301,
ss3799557122,
ss3945063751,
ss4460113679,
ss6351998976,
ss6404017275,
ss6407778568,
ss6494899143,
ss8236871138,
ss8237632433,
ss8243268487,
ss8314396336,
ss8444225829,
ss8516079296,
ss8670383989,
ss8800847089,
ss8849027752,
ss8909410649,
ss8982017092,
ss8982072041,
ss8989718287
</td>
<td>
NC_000001.11:97305363:C:T
</td>
<td>
NC_000001.11:97305363:C:T
</td>
<td>
(self)
</td>
</tr>
<tr>
<td>
ss86237232,
ss86342029,
ss159698104
</td>
<td>
NT_032977.9:67742837:C:T
</td>
<td>
NC_000001.11:97305363:C:T
</td>
<td>
(self)
</td>
</tr>
</tbody>
</table>
</div>
</div>
<div id="publications" class="js-tabcontent">
<a data-width="640px" href="#publications_tp"
ref="section=Publications&action=Click-on-Tooltip&label=publications_tp"
data-section="Publications" data-ga-action="Click-on-Tooltip"
data-ga-label="publications_tp" class="fa fa-question-circle align-right ncbiPopper">
<span class="usa-sr-only">Help</span>
</a>
<p id="publications_tp">
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.</p>
<div class="sect_heading">
26
citations for rs1801160
</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/8698850"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">8698850</a>
</td>
<td class="fir_col">Molecular basis of the human dihydropyrimidine dehydrogenase deficiency and 5-fluorouracil toxicity.</td>
<td>Wei X et al.</td>
<td>1996</td>
<td>The Journal of clinical investigation</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/9723824"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">9723824</a>
</td>
<td class="fir_col">Dihydropyrimidine dehydrogenase pharmacogenetics in Caucasian subjects.</td>
<td>Ridge SA et al.</td>
<td>1998</td>
<td>British journal of clinical pharmacology</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/15132136"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">15132136</a>
</td>
<td class="fir_col">Dihydropyrimidine dehydrogenase pharmacogenetics in the Taiwanese population.</td>
<td>Hsiao HH et al.</td>
<td>2004</td>
<td>Cancer chemotherapy and pharmacology</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/16115930"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">16115930</a>
</td>
<td class="fir_col">Analysis of the DPYD gene implicated in 5-fluorouracil catabolism in a cohort of Caucasian individuals.</td>
<td>Seck K et al.</td>
<td>2005</td>
<td>Clinical cancer research </td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/18452418"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">18452418</a>
</td>
<td class="fir_col">Analysis of the DPYD gene implicated in 5-fluorouracil catabolism in Chinese cancer patients.</td>
<td>He YF et al.</td>
<td>2008</td>
<td>Journal of clinical pharmacy and therapeutics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/19104657"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">19104657</a>
</td>
<td class="fir_col">Strong association of a common dihydropyrimidine dehydrogenase gene polymorphism with fluoropyrimidine-related toxicity in cancer patients.</td>
<td>Gross E et al.</td>
<td>2008</td>
<td>PloS one</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/19473056"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">19473056</a>
</td>
<td class="fir_col">Influence of dihydropyrimidine dehydrogenase gene (DPYD) coding sequence variants on the development of fluoropyrimidine-related toxicity in patients with high-grade toxicity and patients with excellent tolerance of fluoropyrimidine-based chemotherapy.</td>
<td>Kleibl Z et al.</td>
<td>2009</td>
<td>Neoplasma</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/21362212"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">21362212</a>
</td>
<td class="fir_col">[Detection of single nucleotide polymorphisms of mthfr and dpyd genes in leukemia cell lines K562 and K562/A02].</td>
<td>Zhang WJ et al.</td>
<td>2011</td>
<td>Zhongguo shi yan xue ye xue za zhi</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/21498394"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">21498394</a>
</td>
<td class="fir_col">Relationship between single nucleotide polymorphisms and haplotypes in DPYD and toxicity and efficacy of capecitabine in advanced colorectal cancer.</td>
<td>Deenen MJ et al.</td>
<td>2011</td>
<td>Clinical cancer research </td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/23988873"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">23988873</a>
</td>
<td class="fir_col">Clinical Pharmacogenetics Implementation Consortium guidelines for dihydropyrimidine dehydrogenase genotype and fluoropyrimidine dosing.</td>
<td>Caudle KE et al.</td>
<td>2013</td>
<td>Clinical pharmacology and therapeutics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/25110414"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">25110414</a>
</td>
<td class="fir_col">Pharmacogenetics research on chemotherapy resistance in colorectal cancer over the last 20 years.</td>
<td>Panczyk M et al.</td>
<td>2014</td>
<td>World journal of gastroenterology</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/25741868"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">25741868</a>
</td>
<td class="fir_col">Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.</td>
<td>Richards S et al.</td>
<td>2015</td>
<td>Genetics in medicine </td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/26099996"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">26099996</a>
</td>
<td class="fir_col">Clinical validity of a DPYD-based pharmacogenetic test to predict severe toxicity to fluoropyrimidines.</td>
<td>Toffoli G et al.</td>
<td>2015</td>
<td>International journal of cancer</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/26216193"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">26216193</a>
</td>
<td class="fir_col">Genotype-phenotype correlations in 5-fluorouracil metabolism: a candidate DPYD haplotype to improve toxicity prediction.</td>
<td>Gentile G et al.</td>
<td>2016</td>
<td>The pharmacogenomics journal</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/28745575"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">28745575</a>
</td>
<td class="fir_col">Use of exome sequencing to determine the full profile of genetic variants in the fluoropyrimidine pathway in colorectal cancer patients affected by severe toxicity.</td>
<td>Pellicer M et al.</td>
<td>2017</td>
<td>Pharmacogenomics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/29065426"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">29065426</a>
</td>
<td class="fir_col">Dihydropyrimidine dehydrogenase pharmacogenetics for predicting fluoropyrimidine-related toxicity in the randomised, phase III adjuvant TOSCA trial in high-risk colon cancer patients.</td>
<td>Ruzzo A et al.</td>
<td>2017</td>
<td>British journal of cancer</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/29372689"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">29372689</a>
</td>
<td class="fir_col">DPYD genotype and haplotype analysis and colorectal cancer susceptibility in a case-control study from Slovakia.</td>
<td>Matáková T et al.</td>
<td>2017</td>
<td>General physiology and biophysics</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/30545124"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">30545124</a>
</td>
<td class="fir_col">Use of Germline Genetic Variability for Prediction of Chemoresistance and Prognosis of Breast Cancer Patients.</td>
<td>Hlavac V et al.</td>
<td>2018</td>
<td>Cancers</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/32619063"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">32619063</a>
</td>
<td class="fir_col">Impact of DPYD, DPYS, and UPB1 gene variations on severe drug-related toxicity in patients with cancer.</td>
<td>Yokoi K et al.</td>
<td>2020</td>
<td>Cancer science</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/33941060"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">33941060</a>
</td>
<td class="fir_col">DPYD variant testing in candidates for fluoropyrimidine treatment: A study protocol.</td>
<td>Hernández-Guío A et al.</td>
<td>2021</td>
<td>Farmacia hospitalaria </td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/34429635"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">34429635</a>
</td>
<td class="fir_col">Population Genetic Difference of Pharmacogenomic VIP Variants in the Tibetan Population.</td>
<td>He C et al.</td>
<td>2021</td>
<td>Pharmacogenomics and personalized medicine</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/34780066"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">34780066</a>
</td>
<td class="fir_col">DPYD polymorphisms c.496A>G, c.2194G>A and c.85T>C and risk of severe adverse drug reactions in patients treated with fluoropyrimidine-based protocols.</td>
<td>Božina N et al.</td>
<td>2022</td>
<td>British journal of clinical pharmacology</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/35207713"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">35207713</a>
</td>
<td class="fir_col">Elevated Risk of Fluoropyrimidine-Associated Toxicity in European Patients with DPYD Genetic Polymorphism: A Systematic Review and Meta-Analysis.</td>
<td>Kim W et al.</td>
<td>2022</td>
<td>Journal of personalized medicine</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/35582139"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">35582139</a>
</td>
<td class="fir_col">The use of pharmacogenetics to increase the safety of colorectal cancer patients treated with fluoropyrimidines.</td>
<td>De Mattia E et al.</td>
<td>2019</td>
<td>Cancer drug resistance (Alhambra, Calif.)</td>
</tr>
<tr>
<td><a target="_blank" href="/pubmed/36980706"
ref="section=Publications&action=Click-on&label=PMID_link"
data-section="Publications" data-ga-action="Click-on"
data-ga-label="PMID_link">36980706</a>
</td>
<td class="fir_col">Influence of Single-Nucleotide Polymorphisms on Clinical Outcomes of Capecitabine-Based Chemotherapy in Colorectal Cancer Patients: A Systematic Review.</td>
<td>Cura Y et al.</td>
<td>2023</td>
<td>Cancers</td>
</tr>
</tbody>
</table>
</div>
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href="/pubmed?term=8698850,9723824,15132136,16115930,18452418,19104657,19473056,21362212,21498394,23988873,25110414,25741868,26099996,26216193,28745575,29065426,29372689,30545124,32619063,33519226,33941060,34429635,34780066,35207713,35582139,36980706"
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<div id="flanks" class="js-tabcontent">
<a data-width="640px" href="#flanks_tp"
ref="section=Flanks&action=Click-on-Tooltip&label=flanks_tp"
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<p id="flanks_tp">The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.</p>
<div id="flanks_container">
<div id="context_container">
<span class="sect_heading">
Genome context:
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seq_acc_ver="NC_000001.11" position="97305364"
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GRCh38.p14 ( NC_000001.11 )
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GRCh37.p13 ( NC_000001.10 )
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NG_008807.2
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).<br/>
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GRCh38.p14 ( NC_000001.11 )
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GRCh37.p13 ( NC_000001.10 )
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