{"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:3765,10,HGNC:3765,57,1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:3765","source":"HGNC:3765|fms related receptor tyrosine kinase 3","targets":["1092736|NM_004119.3(FLT3):c.1519A>G (p.Ile507Val)|single nucleotide variant|Likely benign|FLT3|criteria provided, single submitter|13","1175588|NM_004119.3(FLT3):c.1309+173T>C|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1178009|NM_004119.3(FLT3):c.2958G>A (p.Pro986=)|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1178254|NM_004119.3(FLT3):c.1206-205A>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1221647|NM_004119.3(FLT3):c.2053+59G>A|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1224230|NM_004119.3(FLT3):c.2054-273A>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1224799|NM_004119.3(FLT3):c.1418+81A>G|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1226610|NM_004119.3(FLT3):c.1683A>G (p.Leu561=)|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1226703|NM_004119.3(FLT3):c.44-81T>C|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1226785|NM_004119.3(FLT3):c.484+81C>T|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1226990|NM_004119.3(FLT3):c.1597+233C>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1227575|NM_004119.3(FLT3):c.1206-313C>T|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1228322|NM_004119.3(FLT3):c.2054-243G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1228527|NM_004119.3(FLT3):c.1206-244G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1228796|NM_004119.3(FLT3):c.615-228G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1229279|NM_004119.3(FLT3):c.369-269T>C|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1230721|NM_004119.3(FLT3):c.2418+128G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1231363|NM_004119.3(FLT3):c.2542-304G>C|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1232565|NM_004119.3(FLT3):c.1942+108A>T|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1232922|NM_004119.3(FLT3):c.165+269C>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1233914|NC_000013.11:g.28100741C>T|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1234126|NM_004119.3(FLT3):c.166-240C>T|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1235360|NM_004119.3(FLT3):c.1598-267A>C|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1235679|NM_004119.3(FLT3):c.369-343G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1241612|NM_004119.3(FLT3):c.1943-179A>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1243109|NM_004119.3(FLT3):c.2753+27G>A|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1245510|NM_004119.3(FLT3):c.2541+58A>G|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1246196|NM_004119.3(FLT3):c.1309+345G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1251597|NM_004119.3(FLT3):c.20A>G (p.Asp7Gly)|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1252193|NM_004119.3(FLT3):c.615-15C>A|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1253421|NM_004119.3(FLT3):c.882+13G>A|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1253749|NM_004119.3(FLT3):c.1419-36T>A|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1253763|NM_004119.3(FLT3):c.2419-187G>A|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1256816|NM_004119.3(FLT3):c.485-214G>C|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1256865|NM_004119.3(FLT3):c.2653+65G>C|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1257200|NM_004119.3(FLT3):c.2053+67CT[9]|Microsatellite|Benign|FLT3|criteria provided, single submitter|13","1260309|NM_004119.3(FLT3):c.165+118G>T|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1263141|NM_004119.3(FLT3):c.883-25C>A|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1263811|NM_004119.3(FLT3):c.166-106G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1265575|NM_004119.3(FLT3):c.1206-285T>C|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1265822|NM_004119.3(FLT3):c.1942+35A>C|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1268770|NM_004119.3(FLT3):c.743-36dup|Duplication|Benign|FLT3|criteria provided, single submitter|13","1269860|NM_004119.3(FLT3):c.1309+106del|Deletion|Benign|FLT3|criteria provided, single submitter|13","1270334|NM_004119.3(FLT3):c.1942+314C>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1270594|NM_004119.3(FLT3):c.2291-225C>T|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1273290|NM_004119.3(FLT3):c.2053+67CT[10]|Microsatellite|Benign|FLT3|criteria provided, single submitter|13","1274386|NM_004119.3(FLT3):c.615-184G>T|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1274485|NM_004119.3(FLT3):c.1310-175A>T|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1276512|NM_004119.3(FLT3):c.166-148G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1277163|NM_004119.3(FLT3):c.2654-116G>A|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1277569|NM_004119.3(FLT3):c.368+189C>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1278209|NM_004119.3(FLT3):c.615-72G>A|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1279150|NM_004119.3(FLT3):c.44-256G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1279467|NM_004119.3(FLT3):c.2290+173A>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1280165|NM_004119.3(FLT3):c.288C>T (p.Asp96=)|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1280714|NM_004119.3(FLT3):c.1418+75A>G|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1281899|NM_004119.3(FLT3):c.1205+56C>T|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1282410|NM_004119.3(FLT3):c.2291-335dup|Duplication|Benign|FLT3|criteria provided, single submitter|13","1283693|NM_004119.3(FLT3):c.1206-294T>C|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1283726|NM_004119.3(FLT3):c.2654-102G>C|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1286009|NM_004119.3(FLT3):c.1419-15T>C|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1286527|NM_004119.3(FLT3):c.1205+224C>T|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1286964|NM_004119.3(FLT3):c.2418+300G>A|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1286972|NM_004119.3(FLT3):c.2418+38_2418+39del|Deletion|Benign|FLT3|criteria provided, single submitter|13","1287159|NM_004119.3(FLT3):c.369-326A>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1287287|NM_004119.3(FLT3):c.615-297C>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1287572|NM_004119.3(FLT3):c.44-136A>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1288512|NM_004119.3(FLT3):c.2053+321C>T|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1288964|NM_004119.3(FLT3):c.1597+236A>G|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","1291612|NM_004119.3(FLT3):c.2053+23A>G|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","1291994|NM_004119.3(FLT3):c.1310-3T>C|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","134433|NM_004119.3(FLT3):c.1249A>C (p.Ile417Leu)|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","134434|NM_004119.3(FLT3):c.1669G>A (p.Val557Ile)|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","134435|NM_004119.3(FLT3):c.2050T>C (p.Ser684Pro)|single nucleotide variant|not provided|FLT3|no classification provided|13","134436|NM_004119.3(FLT3):c.46G>C (p.Val16Leu)|single nucleotide variant|Likely benign|FLT3|criteria provided, single submitter|13","134437|NM_004119.3(FLT3):c.2858C>T (p.Ala953Val)|single nucleotide variant|not provided|FLT3|no classification provided|13","134438|NM_004119.3(FLT3):c.2888C>T (p.Ser963Leu)|single nucleotide variant|Likely benign|FLT3|criteria provided, multiple submitters, no conflicts|13","134439|NM_004119.3(FLT3):c.2957C>T (p.Pro986Leu)|single nucleotide variant|not provided|FLT3|no classification provided|13","134440|NM_004119.3(FLT3):c.2918G>A (p.Arg973Gln)|single nucleotide variant|Likely benign|FLT3|criteria provided, single submitter|13","134441|NM_004119.3(FLT3):c.2962G>C (p.Ala988Pro)|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","134442|NM_004119.3(FLT3):c.2971G>A (p.Glu991Lys)|single nucleotide variant|not provided|FLT3|no classification provided|13","134443|NM_004119.3(FLT3):c.190G>A (p.Gly64Arg)|single nucleotide variant|not provided|FLT3|no classification provided|13","134444|NM_004119.3(FLT3):c.452A>G (p.Asn151Ser)|single nucleotide variant|not provided|FLT3|no classification provided|13","134445|NM_004119.3(FLT3):c.605A>G (p.Gln202Arg)|single nucleotide variant|not provided|FLT3|no classification provided|13","134446|NM_004119.3(FLT3):c.580G>A (p.Val194Met)|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","134447|NM_004119.3(FLT3):c.680C>T (p.Thr227Met)|single nucleotide variant|Benign|FLT3|criteria provided, multiple submitters, no conflicts|13","134448|NM_004119.3(FLT3):c.833A>C (p.Asn278Thr)|single nucleotide variant|not provided|FLT3|no classification provided|13","134449|NM_004119.3(FLT3):c.784C>T (p.Leu262Phe)|single nucleotide variant|not provided|FLT3|no classification provided|13","134450|NM_004119.3(FLT3):c.844G>A (p.Gly282Arg)|single nucleotide variant|not provided|FLT3|no classification provided|13","134451|NM_004119.3(FLT3):c.970G>A (p.Asp324Asn)|single nucleotide variant|Likely benign|FLT3|criteria provided, multiple submitters, no conflicts|13","134452|NM_004119.3(FLT3):c.1073A>T (p.Asp358Val)|single nucleotide variant|Benign|FLT3|criteria provided, single submitter|13","134453|NM_004119.3(FLT3):c.1181A>G (p.Gln394Arg)|single nucleotide variant|not provided|FLT3|no classification provided|13","16270|FLT3, INTERNAL TANDEM DUP|Duplication|Pathogenic|FLT3|no assertion criteria provided|","16271|NM_004119.3(FLT3):c.2520_2521insGGATCC (p.Ser840_Asn841insGlySer)|Insertion|Pathogenic|FLT3|no assertion criteria provided|13","16272|NM_004119.3(FLT3):c.2504A>T (p.Asp835Val)|single nucleotide variant|Pathogenic|FLT3|no assertion criteria provided|13","16273|NM_004119.3(FLT3):c.2503G>C (p.Asp835His)|single nucleotide variant|Pathogenic|FLT3|no assertion criteria provided|13","16274|NM_004119.3(FLT3):c.2503G>A (p.Asp835Asn)|single nucleotide variant|Pathogenic|FLT3|no assertion criteria provided|13","16276|NM_004119.3(FLT3):c.2503G>T (p.Asp835Tyr)|single nucleotide variant|Pathogenic|FLT3|no assertion criteria provided|13","16277|NM_004119.3(FLT3):c.2503_2505del (p.Asp835del)|Deletion|Pathogenic|FLT3|no assertion criteria provided|13","16278|NM_004119.3(FLT3):c.1777_1779del (p.Asp593del)|Deletion|Pathogenic|FLT3|no assertion criteria provided|13"]}]}