{"features":[{"highlight":"","caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1449898864;vf=141471780\">rs1449898864</a>","entries":[{"value":"SNP","key":"Class"},{"value":"dbSNP","key":"Source"},{"value":"2:110049837","key":"Location"},{"value":"G/A/T (Forward strand)","key":"Alleles"},{"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:#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":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1449898864;vf=141471780\">Explore this variant</a>"},{"value":"<a href=\"/Homo_sapiens/Variation/Mappings?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1449898864;vf=141471780\">Gene/Transcript Locations</a>","key":null}]}],"header":null}