{"header":null,"features":[{"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1448407091;vf=141347048\">rs1448407091</a>","entries":[{"value":"deletion","key":"Class"},{"value":"dbSNP","key":"Source"},{"value":"2:233222473","key":"Location"},{"value":"A/- (Forward strand)","key":"Alleles"},{"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></ul>","key":"Consequences"},{"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1448407091;vf=141347048\">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=rs1448407091;vf=141347048\">Gene/Transcript Locations</a>"}],"highlight":""}]}