{"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:1787,10,HGNC:1787,172,2]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:1787","source":"HGNC:1787|cyclin dependent kinase inhibitor 2A","targets":["1000204|NM_000077.5(CDKN2A):c.202G&gt;C (p.Ala68Pro)|single nucleotide variant|Conflicting classifications of pathogenicity|CDKN2A|criteria provided, conflicting classifications|9","1001191|NM_000077.5(CDKN2A):c.59C&gt;T (p.Ala20Val)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1003233|NM_058195.4(CDKN2A):c.53C&gt;T (p.Pro18Leu)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1005179|NM_000077.5(CDKN2A):c.320_321delinsTT (p.Arg107Leu)|Indel|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1006674|NC_000009.11:g.(?_21968228)_(21968346_?)dup|Duplication|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1007158|NM_058195.4(CDKN2A):c.182C&gt;G (p.Pro61Arg)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1007699|NM_058195.4(CDKN2A):c.178C&gt;A (p.Leu60Ile)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1007891|NM_000077.5(CDKN2A):c.175G&gt;A (p.Val59Met)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1011164|NM_058195.4(CDKN2A):c.112G&gt;A (p.Gly38Arg)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1012195|NM_000077.5(CDKN2A):c.281T&gt;A (p.Leu94Gln)|single nucleotide variant|Conflicting classifications of pathogenicity|CDKN2A|criteria provided, conflicting classifications|9","1014424|NC_000009.11:g.(?_21968228)_(22160087_?)dup|Duplication|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1014833|NM_000077.5(CDKN2A):c.311T&gt;C (p.Leu104Pro)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1016504|NM_058195.4(CDKN2A):c.81C&gt;G (p.Ile27Met)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1016652|NM_058195.4(CDKN2A):c.98A&gt;G (p.Glu33Gly)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1017702|NM_058195.4(CDKN2A):c.40G&gt;C (p.Ala14Pro)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1018474|NM_058195.4(CDKN2A):c.3G&gt;C (p.Met1Ile)|single nucleotide variant|Conflicting classifications of pathogenicity|CDKN2A|criteria provided, conflicting classifications|9","1021238|NM_000077.5(CDKN2A):c.150+3dup|Duplication|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1022671|NM_000077.5(CDKN2A):c.35C&gt;G (p.Ser12Trp)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1023233|NM_058195.4(CDKN2A):c.37C&gt;T (p.Arg13Cys)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1036620|NM_058195.4(CDKN2A):c.4G&gt;A (p.Val2Met)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1038258|NM_000077.5(CDKN2A):c.295C&gt;A (p.Arg99=)|single nucleotide variant|Conflicting classifications of pathogenicity|CDKN2A|criteria provided, conflicting classifications|9","1041090|NM_058195.4(CDKN2A):c.133C&gt;A (p.Leu45Ile)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1041690|NM_000077.5(CDKN2A):c.86G&gt;C (p.Arg29Pro)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1041797|NM_000077.5(CDKN2A):c.55G&gt;T (p.Ala19Ser)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1042150|NM_000077.5(CDKN2A):c.129_131dup (p.Tyr44dup)|Duplication|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1042953|NM_000077.5(CDKN2A):c.143C&gt;A (p.Pro48Gln)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1043651|NM_058195.4(CDKN2A):c.110C&gt;G (p.Pro37Arg)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1044517|NC_000009.11:g.(?_21968228)_(21974875_?)dup|Duplication|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1045852|NM_000077.5(CDKN2A):c.150G&gt;C (p.Gln50His)|single nucleotide variant|Conflicting classifications of pathogenicity|CDKN2A|criteria provided, conflicting classifications|9","1046804|NM_058195.4(CDKN2A):c.94G&gt;C (p.Gly32Arg)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1052395|NM_000077.5(CDKN2A):c.133G&gt;T (p.Gly45Cys)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1052397|NM_000077.5(CDKN2A):c.207G&gt;T (p.Glu69Asp)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1054175|NM_000077.5(CDKN2A):c.134G&gt;C (p.Gly45Ala)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1056505|NM_058195.4(CDKN2A):c.193+3A&gt;C|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1056639|NM_058195.4(CDKN2A):c.182C&gt;T (p.Pro61Leu)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1058585|NM_000077.5(CDKN2A):c.11C&gt;T (p.Ala4Val)|single nucleotide variant|Conflicting classifications of pathogenicity|CDKN2A|criteria provided, conflicting classifications|9","1059245|NM_000077.5(CDKN2A):c.279G&gt;T (p.Thr93=)|single nucleotide variant|Conflicting classifications of pathogenicity|CDKN2A|criteria provided, conflicting classifications|9","1059393|NM_058195.4(CDKN2A):c.172C&gt;T (p.Gln58Ter)|single nucleotide variant|Likely pathogenic|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1059920|NM_000077.5(CDKN2A):c.41A&gt;G (p.Asp14Gly)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1060114|NM_058195.4(CDKN2A):c.193+6A&gt;T|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1060388|NM_058195.4(CDKN2A):c.193+4G&gt;A|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1060882|NC_000009.11:g.(?_21974667)_(21974875_?)dup|Duplication|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1061502|NM_000077.5(CDKN2A):c.404G&gt;C (p.Gly135Ala)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1062691|NM_000077.5(CDKN2A):c.58G&gt;A (p.Ala20Thr)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1063226|NM_000077.5(CDKN2A):c.244G&gt;A (p.Val82Met)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1063406|NM_000077.5(CDKN2A):c.118G&gt;C (p.Ala40Pro)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1068946|NM_000077.5(CDKN2A):c.34del (p.Ser12fs)|Deletion|Pathogenic|CDKN2A|criteria provided, single submitter|9","1069074|NM_000077.5(CDKN2A):c.126dup (p.Ser43Ter)|Duplication|Pathogenic|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1070481|NC_000009.11:g.(?_21968228)_(22160087_?)del|Deletion|Pathogenic|CDKN2A|criteria provided, single submitter|9","1072356|NM_058195.4(CDKN2A):c.126_127insCA (p.Val43fs)|Insertion|Pathogenic|CDKN2A|criteria provided, single submitter|9","1075589|NM_000077.5(CDKN2A):c.204_205delinsTT (p.Glu69Ter)|Indel|Pathogenic|CDKN2A|criteria provided, single submitter|9","1076895|NC_000009.11:g.(?_21994128)_(21994330_?)del|Deletion|Pathogenic|CDKN2A|criteria provided, single submitter|9","1077933|NM_000077.5(CDKN2A):c.57C&gt;G (p.Ala19=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1078141|NM_058195.4(CDKN2A):c.177G&gt;C (p.Pro59=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1084389|NM_000077.5(CDKN2A):c.150+6dup|Duplication|Likely benign|CDKN2A|criteria provided, single submitter|9","1086368|NM_058195.4(CDKN2A):c.111A&gt;G (p.Pro37=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1086966|NM_000077.5(CDKN2A):c.216C&gt;T (p.Cys72=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, single submitter|9","1088739|NM_000077.5(CDKN2A):c.457+10G&gt;A|single nucleotide variant|Likely benign|CDKN2A|criteria provided, single submitter|9","1089517|NM_058195.4(CDKN2A):c.126T&gt;G (p.Ala42=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1091471|NM_000077.5(CDKN2A):c.120A&gt;T (p.Ala40=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1094339|NM_058195.4(CDKN2A):c.193+9G&gt;C|single nucleotide variant|Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1097623|NM_058195.4(CDKN2A):c.72G&gt;A (p.Val24=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1099059|NM_058195.4(CDKN2A):c.153G&gt;A (p.Arg51=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1099124|NM_000077.5(CDKN2A):c.151-9C&gt;G|single nucleotide variant|Likely benign|CDKN2A|criteria provided, single submitter|9","1101776|NM_000077.5(CDKN2A):c.126T&gt;C (p.Asn42=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1101964|NM_000077.5(CDKN2A):c.12G&gt;A (p.Ala4=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1104292|NM_058195.4(CDKN2A):c.84G&gt;A (p.Pro28=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1114482|NM_058195.4(CDKN2A):c.72G&gt;C (p.Val24=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1115574|NM_058195.4(CDKN2A):c.15C&gt;T (p.Phe5=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1116520|NM_058195.4(CDKN2A):c.135C&gt;T (p.Leu45=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1118189|NM_000077.5(CDKN2A):c.36G&gt;C (p.Ser12=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1118415|NM_058195.4(CDKN2A):c.51G&gt;T (p.Pro17=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1119143|NM_000077.5(CDKN2A):c.372C&gt;T (p.Arg124=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1121460|NM_058195.4(CDKN2A):c.42G&gt;C (p.Ala14=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1121661|NM_058195.4(CDKN2A):c.138G&gt;A (p.Val46=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1123298|NM_000077.5(CDKN2A):c.327C&gt;T (p.Ala109=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1125799|NM_058195.4(CDKN2A):c.42G&gt;A (p.Ala14=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1126443|NM_000077.5(CDKN2A):c.136C&gt;A (p.Arg46=)|single nucleotide variant|Conflicting classifications of pathogenicity|CDKN2A|criteria provided, conflicting classifications|9","1129005|NM_000077.5(CDKN2A):c.302G&gt;C (p.Gly101Ala)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, single submitter|9","1130897|NM_000077.5(CDKN2A):c.91C&gt;T (p.Leu31=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1132894|NM_000077.5(CDKN2A):c.470G&gt;A (p.Ter157=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, single submitter|9","1133481|NM_000077.5(CDKN2A):c.366C&gt;T (p.Gly122=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1135480|NM_000077.5(CDKN2A):c.18G&gt;C (p.Gly6=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, single submitter|9","1136516|NM_000077.5(CDKN2A):c.129T&gt;C (p.Ser43=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1137388|NM_058195.4(CDKN2A):c.93G&gt;C (p.Thr31=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1138677|NM_000077.5(CDKN2A):c.458-8del|Deletion|Likely benign|CDKN2A|criteria provided, single submitter|9","1140549|NM_058195.4(CDKN2A):c.78C&gt;T (p.His26=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1141816|NM_000077.5(CDKN2A):c.308G&gt;A (p.Arg103Gln)|single nucleotide variant|Uncertain significance|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1145248|NM_000077.5(CDKN2A):c.412A&gt;C (p.Arg138=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, single submitter|9","1147579|NM_058195.4(CDKN2A):c.193+10del|Deletion|Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1148400|NM_058195.4(CDKN2A):c.168G&gt;A (p.Gly56=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1148892|NM_058195.4(CDKN2A):c.111A&gt;T (p.Pro37=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1151113|NM_058195.4(CDKN2A):c.42G&gt;T (p.Ala14=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1152133|NM_000077.5(CDKN2A):c.144G&gt;T (p.Pro48=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, single submitter|9","1155510|NM_000077.5(CDKN2A):c.94C&gt;T (p.Leu32=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1156353|NM_000077.5(CDKN2A):c.465C&gt;A (p.Pro155=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, single submitter|9","1157358|NM_058195.4(CDKN2A):c.54G&gt;A (p.Pro18=)|single nucleotide variant|Benign/Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1159632|NM_000077.5(CDKN2A):c.393C&gt;T (p.Arg131=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1160771|NM_000077.5(CDKN2A):c.139A&gt;C (p.Arg47=)|single nucleotide variant|Likely benign|CDKN2A|criteria provided, multiple submitters, no conflicts|9","1161397|NM_058195.4(CDKN2A):c.81C&gt;T (p.Ile27=)|single nucleotide variant|Conflicting classifications of pathogenicity|CDKN2A|criteria provided, conflicting classifications|9"]}]}