{"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs1212271333;vdb=variation;vf=121807260\">rs1212271333</a>","highlight":"","entries":[{"value":"indel","key":"Class"},{"value":"dbSNP","key":"Source"},{"key":"Location","value":"2:224164707-224164710"},{"value":"GGGG/GGG (Forward strand)","key":"Alleles"},{"key":"Consequences","value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#636363\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant located in the intergenic region, between genes\">intergenic variant</span></nobr><li></ul>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs1212271333;vdb=variation;vf=121807260\">Explore this variant</a>"}]},{"entries":[{"key":"Class","value":"SNP"},{"key":"Source","value":"dbSNP"},{"key":"Location","value":"5:88426796"},{"value":"G/C (Forward strand)","key":"Alleles"},{"value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#ff7f50\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant in which a change has occurred within the region of the splice site, either within 1-3 bases of the exon or 3-8 bases of the intron\">splice region variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#7f7f7f\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant that falls in the polypyrimidine tract at 3' end of intron between 17 and 3 bases from the end (acceptor -3 to acceptor -17)\">splice polypyrimidine tract variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#32cd32\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant that changes non-coding exon sequence in a non-coding transcript\">non coding transcript exon variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#02599c\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant occurring within an intron\">intron variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#32cd32\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant of a non coding RNA gene\">non coding transcript variant</span></nobr><li></ul>","key":"Consequences"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578511;vdb=variation;vf=341147073\">Explore this variant</a>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Population?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578511;vdb=variation;vf=341147073\">Population Allele Frequencies</a>","class":"population"},{"key":"ALL","value":"<span class=\"freq base_G\" style=\"width:100px\"></span><span class=\"freq base_C\" style=\"width:0px\"></span><div>G: 1.000, C: 0.000</div>","childOf":"population"},{"key":"AFR","childOf":"population","value":"<span class=\"freq base_C\" style=\"width:0.1px\"></span><span class=\"freq base_G\" style=\"width:99.9px\"></span><div>C: 0.001, G: 0.999</div>"},{"key":"AMR","value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>","childOf":"population"},{"key":"EAS","childOf":"population","value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>"},{"key":"EUR","childOf":"population","value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>"},{"value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>","childOf":"population","key":"SAS"}],"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578511;vdb=variation;vf=341147073\">rs543578511</a>","highlight":""},{"entries":[{"value":"SNP","key":"Class"},{"value":"dbSNP","key":"Source"},{"key":"Location","value":"5:917649"},{"key":"Alleles","value":"C/A (Forward strand)"},{"key":"Consequences","value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#7ac5cd\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A UTR variant of the 3' UTR\">3 prime UTR variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#02599c\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant occurring within an intron\">intron variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#32cd32\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant of a non coding RNA gene\">non coding transcript variant</span></nobr><li></ul>"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578521;vdb=variation;vf=341147074\">Explore this variant</a>","key":null},{"value":"<a href=\"/Homo_sapiens/Variation/Population?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578521;vdb=variation;vf=341147074\">Population Allele Frequencies</a>","class":"population","key":null},{"value":"<span class=\"freq base_A\" style=\"width:0px\"></span><span class=\"freq base_C\" style=\"width:100px\"></span><div>A: 0.000, C: 1.000</div>","childOf":"population","key":"ALL"},{"key":"AFR","value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>","childOf":"population"},{"value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>","childOf":"population","key":"AMR"},{"value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>","childOf":"population","key":"EAS"},{"key":"EUR","value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>","childOf":"population"},{"key":"SAS","childOf":"population","value":"<span class=\"freq base_A\" style=\"width:0.2px\"></span><span class=\"freq base_C\" style=\"width:99.8px\"></span><div>A: 0.002, C: 0.998</div>"}],"highlight":"","caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578521;vdb=variation;vf=341147074\">rs543578521</a>"},{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578566;vdb=variation;vf=341147075\">rs543578566</a>","highlight":"","entries":[{"key":"Class","value":"SNP"},{"key":"Source","value":"dbSNP"},{"value":"5:75538331","key":"Location"},{"value":"G/A (Forward strand)","key":"Alleles"},{"key":"Consequences","value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#02599c\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant occurring within an intron\">intron variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#ff4500\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A variant in a transcript that is the target of NMD\">NMD transcript variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#32cd32\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A transcript variant of a non coding RNA gene\">non coding transcript variant</span></nobr><li><li><nobr><span class=\"colour\" style=\"background-color:#a52a2a\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant located within a regulatory region\">regulatory region variant</span></nobr><li></ul>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578566;vdb=variation;vf=341147075\">Explore this variant</a>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Population?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578566;vdb=variation;vf=341147075\">Population Allele Frequencies</a>","class":"population"},{"value":"<span class=\"freq base_A\" style=\"width:0px\"></span><span class=\"freq base_G\" style=\"width:100px\"></span><div>A: 0.000, G: 1.000</div>","childOf":"population","key":"ALL"},{"key":"AFR","childOf":"population","value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>"},{"key":"AMR","value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>","childOf":"population"},{"key":"EAS","childOf":"population","value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>"},{"value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>","childOf":"population","key":"EUR"},{"key":"SAS","value":"<span class=\"freq base_G\" style=\"width:99.9px\"></span><span class=\"freq base_A\" style=\"width:0.1px\"></span><div>G: 0.999, A: 0.001</div>","childOf":"population"}]}],"header":null}