{"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:6342,10,HGNC:6342,84,0]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:6342","source":"HGNC:6342|KIT proto-oncogene, receptor tyrosine kinase","targets":["1000223|NM_000222.3(KIT):c.455A>G (p.Gln152Arg)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1000538|NM_000222.3(KIT):c.1471T>C (p.Cys491Arg)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1001121|NM_000222.3(KIT):c.2813A>G (p.Asn938Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1001189|NM_000222.3(KIT):c.2791del (p.Ser931fs)|Deletion|Uncertain significance|KIT|criteria provided, single submitter|4","1001785|NM_000222.3(KIT):c.1880C>T (p.Pro627Leu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1003941|NM_000222.3(KIT):c.2546A>G (p.Glu849Gly)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1004231|NM_000222.3(KIT):c.1399C>T (p.Pro467Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1004480|NM_000222.3(KIT):c.577A>C (p.Lys193Gln)|single nucleotide variant|Conflicting classifications of pathogenicity|KIT|criteria provided, conflicting classifications|4","1004598|NM_000222.3(KIT):c.106C>A (p.Pro36Thr)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1004678|NM_000222.3(KIT):c.2818G>C (p.Ala940Pro)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1005154|NM_000222.3(KIT):c.2258C>T (p.Thr753Ile)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1005181|NM_000222.3(KIT):c.2132A>C (p.Glu711Ala)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1006429|NM_000222.3(KIT):c.2147A>G (p.Asp716Gly)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1007323|NM_000222.3(KIT):c.1699A>C (p.Asn567His)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1008003|NM_000222.3(KIT):c.13C>G (p.Arg5Gly)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1009134|NM_000222.3(KIT):c.1951A>G (p.Met651Val)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1009540|NM_000222.3(KIT):c.1057A>G (p.Arg353Gly)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1009696|NM_000222.3(KIT):c.662A>G (p.Tyr221Cys)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1009776|NM_000222.3(KIT):c.2462C>G (p.Ser821Cys)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1010349|NM_000222.3(KIT):c.406T>C (p.Cys136Arg)|single nucleotide variant|Conflicting classifications of pathogenicity|KIT|criteria provided, conflicting classifications|4","1010376|NM_000222.3(KIT):c.952A>C (p.Met318Leu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1010521|NM_000222.3(KIT):c.2234-3C>A|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1010667|NM_000222.3(KIT):c.2233+6T>G|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1011105|NM_000222.3(KIT):c.500A>G (p.Lys167Arg)|single nucleotide variant|Conflicting classifications of pathogenicity|KIT|criteria provided, conflicting classifications|4","1011454|NM_000222.3(KIT):c.2104C>T (p.Leu702Phe)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1011706|NM_000222.3(KIT):c.1898A>T (p.Glu633Val)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1011919|NM_000222.3(KIT):c.1637A>G (p.Lys546Arg)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1013725|NM_000222.3(KIT):c.2185T>G (p.Ser729Ala)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1013728|NM_000222.3(KIT):c.1876A>G (p.Lys626Glu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1013731|NM_000222.3(KIT):c.2539A>G (p.Thr847Ala)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1013988|NM_000222.3(KIT):c.1647+5C>A|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1014180|NM_000222.3(KIT):c.1517T>C (p.Phe506Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1015278|NM_000222.3(KIT):c.2350G>T (p.Ala784Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1015564|NM_000222.3(KIT):c.2596+6A>G|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1015677|NM_000222.3(KIT):c.659G>C (p.Ser220Thr)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1015824|NM_000222.3(KIT):c.287C>A (p.Thr96Lys)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1015884|NM_000222.3(KIT):c.1255G>C (p.Asp419His)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1015915|NM_000222.3(KIT):c.2803-1G>T|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1016038|NM_000222.3(KIT):c.256A>G (p.Lys86Glu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1016059|NM_000222.3(KIT):c.1952T>A (p.Met651Lys)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1016858|NM_000222.3(KIT):c.1847C>A (p.Ala616Glu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1018146|NM_000222.3(KIT):c.859G>T (p.Val287Leu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1018694|NM_000222.3(KIT):c.115A>G (p.Ile39Val)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1018720|NM_000222.3(KIT):c.1166C>G (p.Thr389Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1018895|NM_000222.3(KIT):c.512T>C (p.Met171Thr)|single nucleotide variant|Conflicting classifications of pathogenicity|KIT|criteria provided, conflicting classifications|4","1019565|NM_000222.3(KIT):c.1880-3T>C|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1019628|NM_000222.3(KIT):c.2709G>A (p.Met903Ile)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1019650|NM_000222.3(KIT):c.1597G>A (p.Ala533Thr)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1020216|NM_000222.3(KIT):c.1346+6A>G|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1020756|NM_000222.3(KIT):c.2611C>T (p.Pro871Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1020781|NM_000222.3(KIT):c.70T>C (p.Ser24Pro)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1020941|NM_000222.3(KIT):c.2057G>T (p.Arg686Leu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1021300|NM_000222.3(KIT):c.2819C>G (p.Ala940Gly)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1021542|NM_000222.3(KIT):c.872A>G (p.Tyr291Cys)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1022152|NM_000222.3(KIT):c.2611C>A (p.Pro871Thr)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1022164|NM_000222.3(KIT):c.2696+5G>A|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1022233|NM_000222.3(KIT):c.303C>G (p.His101Gln)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1022372|NM_000222.3(KIT):c.1021C>T (p.Pro341Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1022658|NM_000222.3(KIT):c.275C>G (p.Thr92Ser)|single nucleotide variant|Conflicting classifications of pathogenicity|KIT|criteria provided, conflicting classifications|4","1022702|NM_000222.3(KIT):c.2802+5G>A|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1023471|NM_000222.3(KIT):c.2180G>T (p.Gly727Val)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1023528|NM_000222.3(KIT):c.1626T>G (p.Ile542Met)|single nucleotide variant|Conflicting classifications of pathogenicity|KIT|criteria provided, conflicting classifications|4","1023943|NM_000222.3(KIT):c.2246A>T (p.Glu749Val)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1024022|NM_000222.3(KIT):c.962C>G (p.Thr321Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1024148|NM_000222.3(KIT):c.1647+4A>G|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1024239|NM_000222.3(KIT):c.1115+4A>C|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1024338|NM_000222.3(KIT):c.386A>G (p.Asp129Gly)|single nucleotide variant|Conflicting classifications of pathogenicity|KIT|criteria provided, conflicting classifications|4","1025684|NM_000222.3(KIT):c.1289C>T (p.Ala430Val)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1025737|NM_000222.3(KIT):c.475G>C (p.Asp159His)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1025968|NM_000222.3(KIT):c.95G>A (p.Gly32Glu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1026234|NM_000222.3(KIT):c.58G>A (p.Val20Ile)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1026486|NM_000222.3(KIT):c.2235C>T (p.Gly745=)|single nucleotide variant|Likely benign|KIT|criteria provided, multiple submitters, no conflicts|4","1026863|NM_000222.3(KIT):c.2717G>C (p.Cys906Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1027202|NM_000222.3(KIT):c.1557C>A (p.His519Gln)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1027329|NM_000222.3(KIT):c.251C>A (p.Thr84Lys)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1029723|NM_000222.3(KIT):c.2024A>G (p.Tyr675Cys)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1034922|NM_000222.3(KIT):c.1025A>G (p.Lys342Arg)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1034938|NM_000222.3(KIT):c.2354C>G (p.Ser785Cys)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1035185|NM_000222.3(KIT):c.1666C>G (p.Gln556Glu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1035477|NM_000222.3(KIT):c.2126C>T (p.Ser709Leu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1035865|NM_000222.3(KIT):c.503C>A (p.Ala168Glu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1036847|NM_000222.3(KIT):c.1375G>A (p.Val459Met)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1037015|NM_000222.3(KIT):c.2695A>C (p.Met899Leu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1037272|NM_000222.3(KIT):c.2773G>C (p.Glu925Gln)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1037368|NM_000222.3(KIT):c.340C>A (p.Pro114Thr)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1037520|NM_000222.3(KIT):c.2601C>A (p.Ser867Arg)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1037658|NM_000222.3(KIT):c.1914G>A (p.Met638Ile)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1039082|NM_000222.3(KIT):c.2393T>C (p.Ile798Thr)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1039799|NM_000222.3(KIT):c.2270T>C (p.Met757Thr)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1039886|NM_000222.3(KIT):c.2114A>G (p.Asn705Ser)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1039889|NM_000222.3(KIT):c.925+6T>C|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1040511|NM_000222.3(KIT):c.1188T>A (p.Asn396Lys)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1041452|NM_000222.3(KIT):c.2584C>G (p.Leu862Val)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1043408|NM_000222.3(KIT):c.2233+4A>T|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1043536|NM_000222.3(KIT):c.385G>C (p.Asp129His)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1043894|NM_000222.3(KIT):c.1618G>T (p.Val540Leu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1043896|NM_000222.3(KIT):c.2113A>C (p.Asn705His)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4","1043931|NM_000222.3(KIT):c.2179G>C (p.Gly727Arg)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1043972|NM_000222.3(KIT):c.569A>T (p.Gln190Leu)|single nucleotide variant|Uncertain significance|KIT|criteria provided, multiple submitters, no conflicts|4","1044067|NM_000222.3(KIT):c.544C>G (p.Leu182Val)|single nucleotide variant|Uncertain significance|KIT|criteria provided, single submitter|4"]}]}