{"header":null,"features":[{"entries":[{"key":"Class","value":"SNP"},{"value":"dbSNP","key":"Source"},{"key":"Location","value":"2:218806644"},{"key":"Alleles","value":"G/A/T (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><li><nobr><span class=\"colour\" style=\"background-color:#a52a2a\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A sequence variant located within a transcription factor binding site\">TF binding site</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>"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1236479631;vf=123815833\">Explore this variant</a>","key":null},{"value":"<a href=\"/Homo_sapiens/Variation/Mappings?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1236479631;vf=123815833\">Gene/Transcript Locations</a>","key":null}],"highlight":"","caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1236479631;vf=123815833\">rs1236479631</a>"}]}