{"header":null,"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1273520868;vf=126880368\">rs1273520868</a>","entries":[{"value":"SNP","key":"Class"},{"value":"dbSNP","key":"Source"},{"value":"2:203442098","key":"Location"},{"value":"A/G (Forward strand)","key":"Alleles"},{"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></ul>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1273520868;vf=126880368\">Explore this variant</a>"},{"value":"<a href=\"/Homo_sapiens/Variation/Mappings?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1273520868;vf=126880368\">Gene/Transcript Locations</a>","key":null}],"highlight":""}]}