{"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578614;vdb=variation;vf=341147080\">rs543578614</a>","highlight":"","entries":[{"value":"SNP","key":"Class"},{"key":"Source","value":"dbSNP"},{"value":"5:156683711","key":"Location"},{"key":"Alleles","value":"G/A/C (Forward strand)"},{"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:#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=rs543578614;vdb=variation;vf=341147080\">Explore this variant</a>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Mappings?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578614;vdb=variation;vf=341147080\">Gene/Transcript Locations</a>"},{"key":null,"class":"population","value":"<a href=\"/Homo_sapiens/Variation/Population?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578614;vdb=variation;vf=341147080\">Population Allele Frequencies</a>"},{"value":"<span class=\"freq base_G\" style=\"width:100px\"></span><span class=\"freq base_A\" style=\"width:0px\"></span><div>G: 1.000, A: 0.000</div>","childOf":"population","key":"ALL"},{"childOf":"population","key":"AFR","value":"<span class=\"freq base_A\" style=\"width:0.2px\"></span><span class=\"freq base_G\" style=\"width:99.8px\"></span><div>A: 0.002, G: 0.998</div>"},{"childOf":"population","key":"AMR","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>","key":"EAS","childOf":"population"},{"value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>","childOf":"population","key":"EUR"},{"childOf":"population","key":"SAS","value":"<span class=\"freq base_G\" style=\"width:100px\"></span><div>G: 1.000</div>"}]},{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578618;vdb=variation;vf=341147081\">rs543578618</a>","highlight":"","entries":[{"key":"Class","value":"SNP"},{"key":"Source","value":"dbSNP"},{"key":"Location","value":"5:10379108"},{"key":"Alleles","value":"A/C (Forward strand)"},{"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></ul>"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578618;vdb=variation;vf=341147081\">Explore this variant</a>","key":null},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Population?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578618;vdb=variation;vf=341147081\">Population Allele Frequencies</a>","class":"population"},{"value":"<span class=\"freq base_A\" style=\"width:100px\"></span><span class=\"freq base_C\" style=\"width:0px\"></span><div>A: 1.000, C: 0.000</div>","key":"ALL","childOf":"population"},{"value":"<span class=\"freq base_C\" style=\"width:0.2px\"></span><span class=\"freq base_A\" style=\"width:99.8px\"></span><div>C: 0.002, A: 0.998</div>","key":"AFR","childOf":"population"},{"value":"<span class=\"freq base_A\" style=\"width:100px\"></span><div>A: 1.000</div>","key":"AMR","childOf":"population"},{"childOf":"population","key":"EAS","value":"<span class=\"freq base_A\" style=\"width:100px\"></span><div>A: 1.000</div>"},{"key":"EUR","childOf":"population","value":"<span class=\"freq base_A\" style=\"width:100px\"></span><div>A: 1.000</div>"},{"value":"<span class=\"freq base_A\" style=\"width:100px\"></span><div>A: 1.000</div>","key":"SAS","childOf":"population"}]},{"highlight":"","caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578592;vdb=variation;vf=341147079\">rs543578592</a>","entries":[{"value":"SNP","key":"Class"},{"value":"dbSNP","key":"Source"},{"value":"5:12301257","key":"Location"},{"value":"C/A/T (Forward strand)","key":"Alleles"},{"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":"Consequences"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578592;vdb=variation;vf=341147079\">Explore this variant</a>"},{"key":null,"class":"population","value":"<a href=\"/Homo_sapiens/Variation/Population?db=core;g=ENSG00000176697;r=11:27654893-27720723;source=dbSNP;t=ENST00000395981;v=rs543578592;vdb=variation;vf=341147079\">Population Allele Frequencies</a>"},{"childOf":"population","key":"ALL","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>"},{"value":"<span class=\"freq base_C\" style=\"width:99.2px\"></span><span class=\"freq base_A\" style=\"width:0.8px\"></span><div>C: 0.992, A: 0.008</div>","childOf":"population","key":"AFR"},{"value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>","key":"AMR","childOf":"population"},{"key":"EAS","childOf":"population","value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>"},{"value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>","key":"EUR","childOf":"population"},{"key":"SAS","childOf":"population","value":"<span class=\"freq base_C\" style=\"width:100px\"></span><div>C: 1.000</div>"}]}],"header":null}