{"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:7551,10,HGNC:7551,98,0]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:7551","source":"HGNC:7551|myosin binding protein C3","targets":["1000925|NM_000256.3(MYBPC3):c.2968C>G (p.Pro990Ala)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1001685|NM_000256.3(MYBPC3):c.1270A>T (p.Ser424Cys)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1002029|NM_000256.3(MYBPC3):c.560C>G (p.Pro187Arg)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1002964|NC_000011.9:g.(?_47356583)_(47356770_?)del|Deletion|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1003799|NM_000256.3(MYBPC3):c.1702G>A (p.Val568Ile)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1004745|NM_000256.3(MYBPC3):c.140G>A (p.Ser47Asn)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1005303|NM_000256.3(MYBPC3):c.2067+4C>G|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1005344|NM_000256.3(MYBPC3):c.3112G>A (p.Val1038Met)|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1007207|NM_000256.3(MYBPC3):c.1333A>G (p.Thr445Ala)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1008173|NM_000256.3(MYBPC3):c.2240G>A (p.Gly747Asp)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1009781|NM_000256.3(MYBPC3):c.2538C>G (p.Val846=)|single nucleotide variant|Likely benign|MYBPC3|criteria provided, single submitter|11","1010229|NM_000256.3(MYBPC3):c.2355G>C (p.Glu785Asp)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1012135|NM_000256.3(MYBPC3):c.1843A>G (p.Ser615Gly)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1013320|NM_000256.3(MYBPC3):c.653_654insCTGGTGACCC (p.Lys218delinsAsnTrpTer)|Insertion|Likely pathogenic|MYBPC3|criteria provided, single submitter|11","1014372|NM_000256.3(MYBPC3):c.2624A>G (p.His875Arg)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1014512|NM_000256.3(MYBPC3):c.3688T>C (p.Phe1230Leu)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1014860|NM_000256.3(MYBPC3):c.3G>A (p.Met1Ile)|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1014914|NM_000256.3(MYBPC3):c.407-3C>T|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1015909|NM_000256.3(MYBPC3):c.1606G>C (p.Ala536Pro)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1017936|NM_000256.3(MYBPC3):c.970A>G (p.Ile324Val)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1020277|NM_000256.3(MYBPC3):c.112G>A (p.Val38Met)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1021240|NM_000256.3(MYBPC3):c.1101G>T (p.Lys367Asn)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1021437|NM_000256.3(MYBPC3):c.3346T>G (p.Leu1116Val)|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1022364|NM_000256.3(MYBPC3):c.909-7G>A|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1023692|NM_000256.3(MYBPC3):c.3449G>C (p.Arg1150Thr)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1024304|NM_000256.3(MYBPC3):c.3374T>C (p.Val1125Ala)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1025002|NM_000256.3(MYBPC3):c.2208C>A (p.Phe736Leu)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1025607|NM_000256.3(MYBPC3):c.1915G>A (p.Val639Ile)|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1025716|NM_000256.3(MYBPC3):c.3202C>T (p.Pro1068Ser)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1026413|NM_000256.3(MYBPC3):c.2309-4C>T|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1026549|NM_000256.3(MYBPC3):c.3515A>C (p.Tyr1172Ser)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1027653|NM_000256.3(MYBPC3):c.2132G>A (p.Trp711Ter)|single nucleotide variant|Pathogenic|MYBPC3|no assertion criteria provided|11","1027654|NM_000256.3(MYBPC3):c.2994+1G>A|single nucleotide variant|Likely pathogenic|MYBPC3|no assertion criteria provided|11","1028162|NM_000256.3(MYBPC3):c.1234T>C (p.Phe412Leu)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1028163|NM_000256.3(MYBPC3):c.1930C>T (p.Pro644Ser)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1035073|NM_000256.3(MYBPC3):c.2674C>A (p.Pro892Thr)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1035704|NM_000256.3(MYBPC3):c.770A>G (p.His257Arg)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1035833|NM_000256.3(MYBPC3):c.2888C>T (p.Thr963Ile)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1036525|NM_000256.3(MYBPC3):c.1747G>A (p.Glu583Lys)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1037078|NM_000256.3(MYBPC3):c.2738-7C>A|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1037338|NM_000256.3(MYBPC3):c.1585A>T (p.Thr529Ser)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1037739|NM_000256.3(MYBPC3):c.409T>A (p.Ser137Thr)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1038339|NM_000256.3(MYBPC3):c.2307C>T (p.Ile769=)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1039018|NM_000256.3(MYBPC3):c.56T>C (p.Val19Ala)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1039712|NC_000011.9:g.(?_47360065)_(47360236_?)dup|Duplication|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1040167|NM_000256.3(MYBPC3):c.1654G>A (p.Ala552Thr)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1040603|NM_000256.3(MYBPC3):c.3628C>T (p.Pro1210Ser)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1040685|NM_000256.3(MYBPC3):c.1973C>A (p.Thr658Asn)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1043065|NM_000256.3(MYBPC3):c.947C>T (p.Pro316Leu)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1043232|NM_000256.3(MYBPC3):c.821+5G>C|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1044028|NM_000256.3(MYBPC3):c.3302C>T (p.Thr1101Ile)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1044849|NM_000256.3(MYBPC3):c.1032C>A (p.Asp344Glu)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1046163|NM_000256.3(MYBPC3):c.406+5G>C|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1050896|NM_000256.3(MYBPC3):c.2962G>A (p.Gly988Arg)|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1051058|NM_000256.3(MYBPC3):c.292+3A>G|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1051411|NM_000256.3(MYBPC3):c.1221C>T (p.Gly407=)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1051853|NM_000256.3(MYBPC3):c.412A>G (p.Ser138Gly)|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1053599|NM_000256.3(MYBPC3):c.1687G>T (p.Val563Leu)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1053754|NM_000256.3(MYBPC3):c.2149-80G>A|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1054332|NM_000256.3(MYBPC3):c.3080A>G (p.Asp1027Gly)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1054743|NM_000256.3(MYBPC3):c.1227-3del|Deletion|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1058286|NM_000256.3(MYBPC3):c.2117G>A (p.Gly706Asp)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1058602|NM_000256.3(MYBPC3):c.1955C>G (p.Pro652Arg)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1062531|NM_000256.3(MYBPC3):c.1454A>G (p.Lys485Arg)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1062602|NM_000256.3(MYBPC3):c.2816G>A (p.Arg939Gln)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1063039|NM_000256.3(MYBPC3):c.722T>G (p.Val241Gly)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1063052|NM_000256.3(MYBPC3):c.2708G>T (p.Gly903Val)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1063945|NM_000256.3(MYBPC3):c.3814G>C (p.Val1272Leu)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, single submitter|11","1065134|NM_000256.3(MYBPC3):c.2737+20A>G|single nucleotide variant|Likely benign|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1066750|NM_000256.3(MYBPC3):c.1449_1457+4del|Deletion|Likely pathogenic|MYBPC3|criteria provided, single submitter|11","1067323|NM_000256.3(MYBPC3):c.1624+1G>T|single nucleotide variant|Pathogenic/Likely pathogenic|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1067412|NC_000011.9:g.(?_47362544)_(47368616_?)del|Deletion|Likely pathogenic|MYBPC3|criteria provided, single submitter|11","1067413|NC_000011.9:g.(?_47358756)_47367811del|Deletion|Likely pathogenic|MYBPC3|criteria provided, single submitter|","1068244|NM_000256.3(MYBPC3):c.3191-1G>C|single nucleotide variant|Likely pathogenic|MYBPC3|criteria provided, single submitter|11","1068267|NM_000256.3(MYBPC3):c.654+2T>C|single nucleotide variant|Conflicting classifications of pathogenicity|MYBPC3|criteria provided, conflicting classifications|11","1068427|NM_000256.3(MYBPC3):c.292+1del|Deletion|Likely pathogenic|MYBPC3|criteria provided, single submitter|11","1069672|NC_000011.9:g.(?_47364119)_(47374208_?)del|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1069713|NM_000256.3(MYBPC3):c.3688_3691dup (p.Ser1231fs)|Duplication|Pathogenic|MYBPC3|criteria provided, single submitter|11","1069832|NC_000011.9:g.(?_47353958)_47355505del|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|","1069833|NC_000011.9:g.(?_47360865)_(47369466_?)del|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1069890|NM_000256.3(MYBPC3):c.1730G>A (p.Trp577Ter)|single nucleotide variant|Pathogenic|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1069891|NM_000256.3(MYBPC3):c.1546G>T (p.Glu516Ter)|single nucleotide variant|Pathogenic|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1069892|NM_000256.3(MYBPC3):c.1420G>T (p.Glu474Ter)|single nucleotide variant|Pathogenic|MYBPC3|criteria provided, single submitter|11","1069893|NM_000256.3(MYBPC3):c.1269_1282del (p.Ser424fs)|Deletion|Pathogenic|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1070193|NM_000256.3(MYBPC3):c.514dup (p.Ile172fs)|Duplication|Pathogenic|MYBPC3|criteria provided, single submitter|11","1070637|NM_000256.3(MYBPC3):c.2012_2013insGG (p.Pro672fs)|Insertion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1070911|NM_000256.3(MYBPC3):c.565del (p.Val189fs)|Deletion|Pathogenic/Likely pathogenic|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1071502|NC_000011.10:g.47350113del|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1072518|NM_000256.3(MYBPC3):c.718_724del (p.Glu240fs)|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1073146|NM_000256.3(MYBPC3):c.3424C>T (p.Gln1142Ter)|single nucleotide variant|Pathogenic|MYBPC3|criteria provided, single submitter|11","1074065|NM_000256.3(MYBPC3):c.318del (p.Ala107fs)|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1074099|NC_000011.10:g.47335210del|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1074339|NM_000256.3(MYBPC3):c.2164G>T (p.Glu722Ter)|single nucleotide variant|Pathogenic|MYBPC3|criteria provided, multiple submitters, no conflicts|11","1074856|NM_000256.3(MYBPC3):c.1353del (p.Glu451fs)|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1074858|NM_000256.3(MYBPC3):c.1048_1049del (p.Lys350fs)|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1074948|NM_000256.3(MYBPC3):c.3357C>G (p.Tyr1119Ter)|single nucleotide variant|Pathogenic|MYBPC3|criteria provided, single submitter|11","1075725|NC_000011.9:g.(?_47363401)_47367757del|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|","1075727|NC_000011.9:g.(?_47357416)_(47360310_?)del|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1076196|NM_000256.3(MYBPC3):c.405del (p.Ser137fs)|Deletion|Pathogenic|MYBPC3|criteria provided, single submitter|11","1076719|NM_000256.3(MYBPC3):c.1831G>T (p.Glu611Ter)|single nucleotide variant|Pathogenic|MYBPC3|criteria provided, multiple submitters, no conflicts|11"]}]}