{"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:9967,10,HGNC:9967,159,1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:9967","source":"HGNC:9967|ret proto-oncogene","targets":["1000528|NM_020975.6(RET):c.2464G>T (p.Val822Leu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1000866|NM_020975.6(RET):c.855C>G (p.Phe285Leu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1001110|NM_020975.6(RET):c.1467C>G (p.Asp489Glu)|single nucleotide variant|Conflicting classifications of pathogenicity|RET|criteria provided, conflicting classifications|10","1001213|NM_020975.6(RET):c.452A>T (p.Asn151Ile)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1001262|NM_020975.6(RET):c.3124G>A (p.Asp1042Asn)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1002252|NM_020975.6(RET):c.422G>C (p.Gly141Ala)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1002265|NM_020975.6(RET):c.1639G>A (p.Asp547Asn)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1002688|NM_020975.6(RET):c.2604G>A (p.Met868Ile)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1003396|NM_020975.6(RET):c.212A>G (p.His71Arg)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1004827|NM_020975.6(RET):c.1683C>A (p.Ser561Arg)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1004869|NM_020975.6(RET):c.3305C>T (p.Ser1102Leu)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1005962|NM_020975.6(RET):c.2979C>G (p.Asp993Glu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1006047|NM_020975.6(RET):c.824G>C (p.Gly275Ala)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1006705|NM_020975.6(RET):c.324G>C (p.Lys108Asn)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1007381|NM_020975.6(RET):c.2481G>A (p.Leu827=)|single nucleotide variant|Likely benign|RET|criteria provided, single submitter|10","1008125|NM_020975.6(RET):c.1828A>C (p.Asn610His)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1008648|NM_020975.6(RET):c.3095G>A (p.Gly1032Asp)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1008711|NM_020975.6(RET):c.349C>T (p.Pro117Ser)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1008954|NM_020975.6(RET):c.2945G>T (p.Arg982Leu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1008979|NM_020975.6(RET):c.1058A>C (p.Asp353Ala)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1009074|NM_020975.6(RET):c.2728C>G (p.Gln910Glu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1010142|NM_020975.6(RET):c.3020A>C (p.Lys1007Thr)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1010360|NM_020975.6(RET):c.2583G>T (p.Gly861=)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1010476|NM_020975.6(RET):c.1358G>C (p.Gly453Ala)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1010590|NM_020975.6(RET):c.3187G>A (p.Gly1063Ser)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1011103|NM_020975.6(RET):c.664G>A (p.Glu222Lys)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1011282|NM_020975.6(RET):c.1076A>T (p.Asn359Ile)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1011863|NM_020975.6(RET):c.1042C>T (p.Arg348Trp)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1012555|NM_020975.6(RET):c.936G>A (p.Arg312=)|single nucleotide variant|Benign/Likely benign|RET|criteria provided, multiple submitters, no conflicts|10","1013765|NM_020975.6(RET):c.2765C>T (p.Ser922Phe)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1014445|NM_020975.6(RET):c.1263+9A>G|single nucleotide variant|Likely benign|RET|criteria provided, single submitter|10","1014472|NM_020975.6(RET):c.1882C>T (p.Pro628Ser)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1014605|NM_020975.6(RET):c.1865_1866delinsTT (p.Pro622Leu)|Indel|Uncertain significance|RET|criteria provided, single submitter|10","1015149|NM_020975.6(RET):c.2936A>G (p.Glu979Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1016306|NM_020975.6(RET):c.445TTC[1] (p.Phe150del)|Microsatellite|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1016740|NM_020975.6(RET):c.1537G>A (p.Ala513Thr)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1016923|NM_020975.6(RET):c.3280A>G (p.Ser1094Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1017129|NM_020975.6(RET):c.3138_3139delinsTT (p.Pro1047Ser)|Indel|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1017166|NM_020975.6(RET):c.3247_3254del (p.Thr1083fs)|Deletion|Uncertain significance|RET|criteria provided, single submitter|10","1017413|NC_000010.10:g.(?_43617300)_(43623793_?)dup|Duplication|Uncertain significance|RET|criteria provided, single submitter|10","1018126|NM_020975.6(RET):c.2257A>G (p.Thr753Ala)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1018976|NM_020975.6(RET):c.137C>T (p.Ala46Val)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1019429|NM_020975.6(RET):c.2039C>T (p.Ala680Val)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1019430|NM_020975.6(RET):c.566G>T (p.Arg189Leu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1019577|NM_020975.6(RET):c.3337G>A (p.Asp1113Asn)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1019731|NM_020975.6(RET):c.1046C>G (p.Ala349Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1020551|NM_020975.6(RET):c.2108A>G (p.Gln703Arg)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1020733|NM_020975.6(RET):c.1697C>T (p.Pro566Leu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1021065|NM_020975.6(RET):c.1579G>A (p.Glu527Lys)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1021079|NM_020975.6(RET):c.2779A>C (p.Ile927Leu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1021592|NM_020975.6(RET):c.916G>T (p.Ala306Ser)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1021928|NM_020975.6(RET):c.1910T>G (p.Val637Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1022158|NM_020975.6(RET):c.455C>T (p.Thr152Ile)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1023335|NM_020975.6(RET):c.959C>T (p.Pro320Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|RET|criteria provided, conflicting classifications|10","1026400|NM_020975.6(RET):c.3311C>T (p.Ser1104Leu)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1026781|NM_020975.6(RET):c.2416T>C (p.Tyr806His)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1026784|NM_020975.6(RET):c.2267C>G (p.Ala756Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1034965|NM_020975.6(RET):c.2412G>A (p.Val804=)|single nucleotide variant|Conflicting classifications of pathogenicity|RET|criteria provided, conflicting classifications|10","1035240|NM_020975.6(RET):c.3089ACG[1] (p.Asp1031del)|Microsatellite|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1035325|NM_020975.6(RET):c.2789C>T (p.Thr930Met)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1035737|NM_020975.6(RET):c.3163A>C (p.Thr1055Pro)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1036436|NM_020975.6(RET):c.1985A>G (p.Lys662Arg)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1037025|NM_020975.6(RET):c.751G>A (p.Glu251Lys)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1037635|NM_020975.6(RET):c.1821C>T (p.Gly607=)|single nucleotide variant|Conflicting classifications of pathogenicity|RET|criteria provided, conflicting classifications|10","1038338|NM_020975.6(RET):c.1287C>A (p.Asn429Lys)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1038426|NM_020975.6(RET):c.1310A>G (p.Asn437Ser)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1038777|NM_020975.6(RET):c.3316G>A (p.Ala1106Thr)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1039313|NM_020975.6(RET):c.712G>A (p.Glu238Lys)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1039438|NM_020975.6(RET):c.743G>C (p.Gly248Ala)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1039531|NM_020975.6(RET):c.3196G>A (p.Asp1066Asn)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1039584|NM_020975.6(RET):c.50T>C (p.Leu17Pro)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1039688|NM_020975.6(RET):c.1594G>A (p.Gly532Ser)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1039962|NM_020975.6(RET):c.865G>C (p.Glu289Gln)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1040003|NM_020975.6(RET):c.760G>C (p.Val254Leu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1040021|NM_020975.6(RET):c.1348A>G (p.Ser450Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1040589|NM_020975.6(RET):c.1108A>G (p.Met370Val)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1040791|NM_020975.6(RET):c.2245A>G (p.Arg749Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1041010|NM_020975.6(RET):c.1994A>G (p.His665Arg)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1041457|NM_020975.6(RET):c.1804A>T (p.Ile602Phe)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1041498|NM_020975.6(RET):c.3180A>T (p.Lys1060Asn)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1041508|NM_020975.6(RET):c.3106G>A (p.Glu1036Lys)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1041774|NM_020975.6(RET):c.2900G>A (p.Gly967Asp)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1042395|NM_020975.6(RET):c.2222C>G (p.Ala741Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1044090|NM_020975.6(RET):c.3173A>G (p.Glu1058Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1044947|NM_020975.6(RET):c.565C>T (p.Arg189Cys)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1045058|NM_020975.6(RET):c.2164A>G (p.Lys722Glu)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1045072|NM_020975.6(RET):c.1996A>C (p.Lys666Gln)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1046535|NM_020975.6(RET):c.2954T>G (p.Leu985Arg)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1046889|NM_020975.6(RET):c.2068T>G (p.Ser690Ala)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1051662|NM_020975.6(RET):c.2297C>G (p.Pro766Arg)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1051717|NM_020975.6(RET):c.394C>G (p.Leu132Val)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1052170|NM_020975.6(RET):c.3112A>T (p.Thr1038Ser)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1052683|NM_020975.6(RET):c.3151G>A (p.Ala1051Thr)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1053217|NM_020975.6(RET):c.475T>A (p.Ser159Thr)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10","1054477|NC_000010.10:g.(?_43572512)_(43596180_?)dup|Duplication|Uncertain significance|RET|criteria provided, single submitter|10","1054885|NM_020975.6(RET):c.3056C>G (p.Ala1019Gly)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1054968|NM_020975.6(RET):c.2734C>T (p.Arg912Trp)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1055443|NM_020975.6(RET):c.2557T>C (p.Ser853Pro)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1056160|NM_020975.6(RET):c.385C>G (p.Pro129Ala)|single nucleotide variant|Uncertain significance|RET|criteria provided, single submitter|10","1056765|NM_020975.6(RET):c.160C>T (p.His54Tyr)|single nucleotide variant|Uncertain significance|RET|criteria provided, multiple submitters, no conflicts|10"]}]}