{"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs984568954;vf=110812163\">rs984568954</a>","highlight":"","entries":[{"value":"SNP","key":"Class"},{"key":"Source","value":"dbSNP"},{"key":"Location","value":"2:26970673"},{"key":"Alleles","value":"C/T (Forward strand)"},{"value":"<ul><li><nobr><span class=\"colour\" style=\"background-color:#7ac5cd\">&nbsp;</span>&nbsp;<span class=\"_ht ht\" title=\"A UTR variant of the 5' UTR\">5 prime UTR 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><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":"Consequences"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs984568954;vf=110812163\">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=rs984568954;vf=110812163\">Gene/Transcript Locations</a>"}]}],"header":null}