{"header":null,"features":[{"highlight":"","entries":[{"key":"Class","value":"indel"},{"key":"Source","value":"dbSNP"},{"key":"Location","value":"1:266321-266325"},{"key":"Alleles","value":"ACACA/ACA (Forward strand)"},{"key":"Consequences","value":"<ul><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></ul>"},{"key":null,"value":"<a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1641789424;vf=58206579\">Explore this variant</a>"},{"value":"<a href=\"/Homo_sapiens/Variation/Mappings?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1641789424;vf=58206579\">Gene/Transcript Locations</a>","key":null}],"caption":"Variation: <a href=\"/Homo_sapiens/Variation/Explore?db=core;g=ENSG00000175325;r=5:177992235-177996242;source=dbSNP;t=ENST00000308304;v=rs1641789424;vf=58206579\">rs1641789424</a>"}]}