{"features":[{"highlight":"","caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1455638499;vf=141948509\">rs1455638499</a>","entries":[{"key":"Class","value":"SNP"},{"key":"Source","value":"dbSNP"},{"value":"2:161629934","key":"Location"},{"key":"Alleles","value":"A/G (Forward strand)"},{"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>","key":"Consequences"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1455638499;vf=141948509\">Explore this variant</a>","key":null},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Mappings?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1455638499;vf=141948509\">Gene/Transcript Locations</a>"}]}],"header":null}