{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:7577,10,HGNC:7577,70,1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:7577","source":"HGNC:7577|myosin heavy chain 7","targets":["1000247|NM_000257.4(MYH7):c.1058C>T (p.Thr353Ile)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1000856|NM_000257.4(MYH7):c.2252T>C (p.Ile751Thr)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1001239|NM_000257.4(MYH7):c.2192C>T (p.Pro731Leu)|single nucleotide variant|Likely pathogenic|MYH7|criteria provided, single submitter|14","1001687|NM_000257.4(MYH7):c.3508G>A (p.Glu1170Lys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1002965|NC_000014.8:g.(?_23882053)_(23882090_?)del|Deletion|Uncertain significance|MYH7|criteria provided, single submitter|14","1003930|NM_000257.4(MYH7):c.76G>A (p.Ala26Thr)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1005860|NM_000257.4(MYH7):c.1319T>C (p.Val440Ala)|single nucleotide variant|Conflicting classifications of pathogenicity|MYH7|criteria provided, conflicting classifications|14","1006322|NM_000257.4(MYH7):c.899T>C (p.Met300Thr)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1006817|NM_000257.4(MYH7):c.9T>G (p.Asp3Glu)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1006900|NM_000257.4(MYH7):c.5654C>T (p.Ala1885Val)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1007310|NM_000257.4(MYH7):c.3152C>A (p.Ala1051Glu)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1007714|NM_000257.4(MYH7):c.427C>A (p.Arg143=)|single nucleotide variant|Likely benign|MYH7|criteria provided, single submitter|14","1007904|NM_000257.4(MYH7):c.2766G>T (p.Met922Ile)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1008274|NM_000257.4(MYH7):c.1541G>C (p.Gly514Ala)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1009064|NM_000257.4(MYH7):c.3667G>C (p.Glu1223Gln)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1009156|NM_000257.4(MYH7):c.311A>G (p.Asn104Ser)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1009423|NM_000257.4(MYH7):c.895G>C (p.Asp299His)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1011193|NM_000257.4(MYH7):c.3028C>T (p.Leu1010Phe)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1011280|NM_000257.4(MYH7):c.5602G>A (p.Val1868Ile)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1012134|NM_000257.4(MYH7):c.1791C>G (p.Asn597Lys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1012831|NM_000257.4(MYH7):c.2065G>C (p.Val689Leu)|single nucleotide variant|Likely benign|MYH7|criteria provided, single submitter|14","1013757|NM_000257.4(MYH7):c.3501C>T (p.Arg1167=)|single nucleotide variant|Likely benign|MYH7|criteria provided, multiple submitters, no conflicts|14","1013939|NM_000257.4(MYH7):c.253G>C (p.Asp85His)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1014067|NM_000257.4(MYH7):c.2151C>G (p.Asp717Glu)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1014897|NM_000257.4(MYH7):c.4159G>C (p.Glu1387Gln)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1016479|NM_000257.4(MYH7):c.2214C>G (p.Ser738Arg)|single nucleotide variant|Conflicting classifications of pathogenicity|MYH7|criteria provided, conflicting classifications|14","1017829|NM_000257.4(MYH7):c.3367G>A (p.Glu1123Lys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1018283|NM_000257.4(MYH7):c.2099A>G (p.Glu700Gly)|single nucleotide variant|Conflicting classifications of pathogenicity|MYH7|criteria provided, conflicting classifications|14","1018284|NM_000257.4(MYH7):c.1346C>T (p.Thr449Ile)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1018285|NM_000257.4(MYH7):c.909C>G (p.Ile303Met)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1018305|NM_000257.4(MYH7):c.3470C>A (p.Thr1157Lys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1018988|NM_000257.4(MYH7):c.2916G>C (p.Glu972Asp)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1019506|NM_000257.4(MYH7):c.919C>T (p.Pro307Ser)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1021629|NM_000257.4(MYH7):c.3847G>A (p.Glu1283Lys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1021790|NM_000257.4(MYH7):c.1789A>T (p.Asn597Tyr)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1022713|NM_000257.4(MYH7):c.508_509del (p.Glu170fs)|Microsatellite|Uncertain significance|MYH7|criteria provided, single submitter|14","1022918|NM_000257.4(MYH7):c.2896_2898del (p.Lys966del)|Deletion|Uncertain significance|MYH7|criteria provided, single submitter|14","1023003|NM_000257.4(MYH7):c.1888C>A (p.Pro630Thr)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1023198|NM_000257.4(MYH7):c.758G>A (p.Gly253Glu)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1024345|NM_000257.4(MYH7):c.2224G>C (p.Ala742Pro)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1024639|NM_000257.4(MYH7):c.5503G>C (p.Glu1835Gln)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1024810|NM_000257.4(MYH7):c.937A>G (p.Ile313Val)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1025662|NM_000257.4(MYH7):c.5680T>C (p.Ser1894Pro)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1025672|NM_000257.4(MYH7):c.3341G>C (p.Arg1114Pro)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1025697|NM_000257.4(MYH7):c.3961G>A (p.Glu1321Lys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1026004|NM_000257.4(MYH7):c.166G>A (p.Gly56Ser)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1026181|NM_000257.4(MYH7):c.494T>C (p.Met165Thr)|single nucleotide variant|Likely pathogenic|MYH7|criteria provided, single submitter|14","1027144|NC_000014.8:g.(?_23898144)_(23899892_?)del|Deletion|Uncertain significance|MYH7|criteria provided, single submitter|14","1027658|NM_000257.4(MYH7):c.1572C>G (p.Ile524Met)|single nucleotide variant|Likely pathogenic|MYH7|criteria provided, single submitter|14","1031478|NM_000257.4(MYH7):c.2951G>T (p.Gly984Val)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1034575|NM_000257.4(MYH7):c.2978C>T (p.Thr993Ile)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1035035|NM_000257.4(MYH7):c.1304T>A (p.Met435Lys)|single nucleotide variant|Conflicting classifications of pathogenicity|MYH7|criteria provided, conflicting classifications|14","1035181|NM_000257.4(MYH7):c.5467G>C (p.Glu1823Gln)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1035719|NM_000257.4(MYH7):c.857T>G (p.Phe286Cys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1037017|NM_000257.4(MYH7):c.5773C>T (p.Arg1925Cys)|single nucleotide variant|Conflicting classifications of pathogenicity|MYH7|criteria provided, conflicting classifications|14","1037717|NM_000257.4(MYH7):c.3336+2T>C|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1037729|NM_000257.4(MYH7):c.4006G>A (p.Ala1336Thr)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1038562|NM_000257.4(MYH7):c.292G>A (p.Glu98Lys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1038786|NM_000257.4(MYH7):c.2700T>G (p.Asp900Glu)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1038801|NM_000257.4(MYH7):c.1605A>C (p.Glu535Asp)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1038805|NM_000257.4(MYH7):c.3203A>G (p.Asp1068Gly)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1038979|NM_000257.4(MYH7):c.4190T>C (p.Leu1397Pro)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1039458|NM_000257.4(MYH7):c.152T>C (p.Ile51Thr)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1039470|NM_000257.4(MYH7):c.1753A>G (p.Ile585Val)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1039714|NC_000014.8:g.(?_23885203)_(23885531_?)dup|Duplication|Uncertain significance|MYH7|criteria provided, single submitter|14","1039954|NM_000257.4(MYH7):c.1030G>A (p.Glu344Lys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1040581|NM_000257.4(MYH7):c.3107G>A (p.Gly1036Glu)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1040661|NM_000257.4(MYH7):c.5725C>G (p.Arg1909Gly)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1041888|NM_000257.4(MYH7):c.666G>C (p.Gln222His)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1043587|NM_000257.4(MYH7):c.4145G>T (p.Arg1382Leu)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1044286|NM_000257.4(MYH7):c.896-2A>G|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1045288|NM_000257.4(MYH7):c.5541C>G (p.Ile1847Met)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1045290|NM_000257.4(MYH7):c.1024A>C (p.Thr342Pro)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1045293|NM_000257.4(MYH7):c.1921G>A (p.Gly641Ser)|single nucleotide variant|Conflicting classifications of pathogenicity|MYH7|criteria provided, conflicting classifications|14","1045981|NM_000257.4(MYH7):c.5401del (p.Glu1801fs)|Deletion|Uncertain significance|MYH7|criteria provided, single submitter|14","1046133|NM_000257.4(MYH7):c.706G>T (p.Val236Phe)|single nucleotide variant|Conflicting classifications of pathogenicity|MYH7|criteria provided, conflicting classifications|14","1051122|NM_000257.4(MYH7):c.3499C>G (p.Arg1167Gly)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1051194|NM_000257.4(MYH7):c.1886C>T (p.Ala629Val)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1053980|NM_000257.4(MYH7):c.2024C>T (p.Pro675Leu)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1054170|NM_000257.4(MYH7):c.1977G>A (p.Met659Ile)|single nucleotide variant|Likely pathogenic|MYH7|criteria provided, multiple submitters, no conflicts|14","1057621|NM_000257.4(MYH7):c.2753A>G (p.Lys918Arg)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1058351|NM_000257.4(MYH7):c.1823T>C (p.Leu608Ser)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, multiple submitters, no conflicts|14","1058378|NM_000257.4(MYH7):c.2144A>G (p.Tyr715Cys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1059396|NM_000257.4(MYH7):c.1142C>A (p.Ala381Asp)|single nucleotide variant|Conflicting classifications of pathogenicity|MYH7|criteria provided, conflicting classifications|14","1060056|NM_000257.4(MYH7):c.714C>G (p.Asn238Lys)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1060994|NM_000257.4(MYH7):c.5342G>T (p.Arg1781Leu)|single nucleotide variant|Likely pathogenic|MYH7|criteria provided, multiple submitters, no conflicts|14","1062792|NM_000257.4(MYH7):c.4164G>T (p.Glu1388Asp)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1064218|NM_000257.4(MYH7):c.1387G>A (p.Ala463Thr)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1065184|NM_000257.4(MYH7):c.1997A>G (p.His666Arg)|single nucleotide variant|Uncertain significance|MYH7|criteria provided, single submitter|14","1071112|NM_000257.4(MYH7):c.732+1G>T|single nucleotide variant|Pathogenic|MYH7|criteria provided, single submitter|14","1077955|NM_000257.4(MYH7):c.3891G>A (p.Leu1297=)|single nucleotide variant|Likely benign|MYH7|criteria provided, multiple submitters, no conflicts|14","1079963|NM_000257.4(MYH7):c.5610G>A (p.Lys1870=)|single nucleotide variant|Likely benign|MYH7|criteria provided, single submitter|14","1080854|NM_000257.4(MYH7):c.3727-8C>T|single nucleotide variant|Likely benign|MYH7|criteria provided, multiple submitters, no conflicts|14","1080862|NM_000257.4(MYH7):c.3588C>T (p.His1196=)|single nucleotide variant|Likely benign|MYH7|criteria provided, multiple submitters, no conflicts|14","1081322|NM_000257.4(MYH7):c.3606G>A (p.Glu1202=)|single nucleotide variant|Likely benign|MYH7|criteria provided, single submitter|14","1082144|NM_000257.4(MYH7):c.432C>A (p.Gly144=)|single nucleotide variant|Likely benign|MYH7|criteria provided, multiple submitters, no conflicts|14","1082145|NM_000257.4(MYH7):c.5505G>A (p.Glu1835=)|single nucleotide variant|Likely benign|MYH7|criteria provided, multiple submitters, no conflicts|14","1084112|NM_000257.4(MYH7):c.3954G>A (p.Gln1318=)|single nucleotide variant|Likely benign|MYH7|criteria provided, multiple submitters, no conflicts|14","1084191|NM_000257.4(MYH7):c.3567C>G (p.Ala1189=)|single nucleotide variant|Likely benign|MYH7|criteria provided, single submitter|14","1087234|NM_000257.4(MYH7):c.3894C>A (p.Ile1298=)|single nucleotide variant|Likely benign|MYH7|criteria provided, single submitter|14"]}]}