{"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:7029,10,HGNC:7029,153,-1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:7029","source":"HGNC:7029|MET proto-oncogene, receptor tyrosine kinase","targets":["1000490|NM_000245.4(MET):c.2102+5T>G|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1000580|NM_000245.4(MET):c.4078A>G (p.Lys1360Glu)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1001080|NM_000245.4(MET):c.2573T>G (p.Leu858Arg)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1001112|NM_000245.4(MET):c.554T>A (p.Leu185His)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1001228|NM_000245.4(MET):c.1604T>C (p.Phe535Ser)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1001241|NM_000245.4(MET):c.571C>A (p.Arg191=)|single nucleotide variant|Benign/Likely benign|MET|criteria provided, multiple submitters, no conflicts|7","1001279|NM_000245.4(MET):c.826A>C (p.Thr276Pro)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1001288|NM_000245.4(MET):c.653G>T (p.Arg218Met)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1001428|NM_000245.4(MET):c.654G>C (p.Arg218Ser)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1001674|NM_000245.4(MET):c.3017C>G (p.Thr1006Ser)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1002365|NM_000245.4(MET):c.952C>T (p.Gln318Ter)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1002485|NM_000245.4(MET):c.755C>T (p.Ala252Val)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1003053|NM_000245.4(MET):c.874A>G (p.Met292Val)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1003269|NM_000245.4(MET):c.2614G>A (p.Gly872Ser)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1003317|NC_000007.14:g.(?_116740846)_(116741031_?)del|Deletion|Uncertain significance|MET|criteria provided, single submitter|7","1003318|NC_000007.13:g.(?_116339133)_(116399550_?)dup|Duplication|Uncertain significance|MET|criteria provided, single submitter|7","1003572|NM_000245.4(MET):c.102G>C (p.Glu34Asp)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1003863|NM_000245.4(MET):c.826A>T (p.Thr276Ser)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1004076|NM_000245.4(MET):c.2528C>G (p.Pro843Arg)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1004915|NM_000245.4(MET):c.277C>T (p.Pro93Ser)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1005796|NM_000245.4(MET):c.1568T>G (p.Phe523Cys)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1006167|NM_000245.4(MET):c.3539A>T (p.Asp1180Val)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1006321|NM_000245.4(MET):c.196G>T (p.Ala66Ser)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1006595|NM_000245.4(MET):c.26C>T (p.Pro9Leu)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1006887|NM_000245.4(MET):c.319T>G (p.Leu107Val)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1006899|NM_000245.4(MET):c.2351G>A (p.Arg784Lys)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1007026|NM_000245.4(MET):c.1360A>C (p.Asn454His)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1007265|NM_000245.4(MET):c.1789G>T (p.Asp597Tyr)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1007722|NM_000245.4(MET):c.3215G>A (p.Gly1072Glu)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1007762|NM_000245.4(MET):c.462A>G (p.Ile154Met)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1009066|NM_000245.4(MET):c.1477G>A (p.Glu493Lys)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1009100|NM_000245.4(MET):c.1580G>A (p.Ser527Asn)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1009117|NM_000245.4(MET):c.2267G>A (p.Gly756Asp)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1009184|NM_000245.4(MET):c.2737C>A (p.Gln913Lys)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1009364|NM_000245.4(MET):c.3983C>T (p.Pro1328Leu)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1011423|NM_000245.4(MET):c.3961C>T (p.His1321Tyr)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1012588|GRCh37/hg19 7q31.2(chr7:116395409-116436178)x3|copy number gain|Uncertain significance|MET|criteria provided, single submitter|7","1013952|NM_000245.4(MET):c.625C>T (p.His209Tyr)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1013985|NM_000245.4(MET):c.159G>C (p.Gln53His)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1014297|NM_000245.4(MET):c.2954G>C (p.Ser985Thr)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1014854|NM_000245.4(MET):c.3428T>A (p.Leu1143Gln)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1014865|NM_000245.4(MET):c.2234A>T (p.Tyr745Phe)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1015143|NM_000245.4(MET):c.703A>C (p.Ile235Leu)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1015665|NM_000245.4(MET):c.1597C>A (p.Pro533Thr)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1016149|NM_000245.4(MET):c.122A>G (p.Tyr41Cys)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1016239|NM_000245.4(MET):c.3284G>C (p.Gly1095Ala)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1016629|NM_000245.4(MET):c.2950G>A (p.Val984Ile)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1017937|NM_000245.4(MET):c.1392+6T>G|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1018155|NM_000245.4(MET):c.2114G>A (p.Ser705Asn)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1018416|NM_000245.4(MET):c.2065C>T (p.His689Tyr)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1018484|NM_000245.4(MET):c.1021A>G (p.Ile341Val)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1018553|NM_000245.4(MET):c.3994G>C (p.Glu1332Gln)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1018877|NM_000245.4(MET):c.2128T>C (p.Tyr710His)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1019095|NM_000245.4(MET):c.3437G>A (p.Cys1146Tyr)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1019320|NM_000245.4(MET):c.1318A>C (p.Thr440Pro)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1020037|NM_000245.4(MET):c.387A>T (p.Gln129His)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1020440|NM_000245.4(MET):c.2951T>C (p.Val984Ala)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1020441|NM_000245.4(MET):c.2736G>C (p.Lys912Asn)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1020823|NM_000245.4(MET):c.2092A>G (p.Thr698Ala)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1020846|NM_000245.4(MET):c.3415G>A (p.Val1139Ile)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1021168|NM_000245.4(MET):c.4096C>A (p.Pro1366Thr)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1021217|NM_000245.4(MET):c.1483A>C (p.Thr495Pro)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1021685|NM_000245.4(MET):c.3199C>G (p.Gln1067Glu)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1021858|NM_000245.4(MET):c.3403A>T (p.Ser1135Cys)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1022015|NM_000245.4(MET):c.321A>T (p.Leu107Phe)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1022871|NM_000245.4(MET):c.2569G>A (p.Val857Ile)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1023078|NM_000245.4(MET):c.2806G>T (p.Ala936Ser)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1024064|NC_000007.13:g.(?_116339139)_(116436178_?)dup|Duplication|Uncertain significance|MET|criteria provided, single submitter|7","1024065|NC_000007.13:g.(?_116339139)_(116411718_?)dup|Duplication|Uncertain significance|MET|criteria provided, single submitter|7","1024132|NM_000245.4(MET):c.1527+6C>G|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1024574|NM_000245.4(MET):c.1322C>G (p.Ser441Cys)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1024715|NM_000245.4(MET):c.3155A>G (p.His1052Arg)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1025314|NM_000245.4(MET):c.302G>A (p.Cys101Tyr)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1026230|NM_000245.4(MET):c.2323A>G (p.Met775Val)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1026626|NM_000245.4(MET):c.2437C>T (p.Leu813Phe)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1026890|NM_000245.4(MET):c.239A>G (p.Lys80Arg)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1026935|NM_000245.4(MET):c.1235G>A (p.Arg412His)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1027113|NM_000245.4(MET):c.1527+4A>G|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1027332|NM_000245.4(MET):c.403A>T (p.Ser135Cys)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1034465|NM_000245.4(MET):c.1403C>T (p.Ser468Phe)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1034591|NM_000245.4(MET):c.554T>C (p.Leu185Pro)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1035183|NM_000245.4(MET):c.3986C>T (p.Ser1329Phe)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1035802|NM_000245.4(MET):c.1072G>C (p.Asp358His)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1035944|NM_000245.4(MET):c.166A>G (p.Ile56Val)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1036004|NM_000245.4(MET):c.2043C>G (p.Tyr681Ter)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1036057|NM_000245.4(MET):c.841T>G (p.Phe281Val)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1036075|NM_000245.4(MET):c.610T>C (p.Ser204Pro)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1036459|NM_000245.4(MET):c.914A>G (p.Lys305Arg)|single nucleotide variant|Conflicting classifications of pathogenicity|MET|criteria provided, conflicting classifications|7","1036576|NM_000245.4(MET):c.3520C>T (p.His1174Tyr)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1036632|NM_000245.4(MET):c.4015G>C (p.Ala1339Pro)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1036967|NM_000245.4(MET):c.891G>C (p.Glu297Asp)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1037932|NM_000245.4(MET):c.1032G>T (p.Gly344=)|single nucleotide variant|Likely benign|MET|criteria provided, multiple submitters, no conflicts|7","1038186|NM_000245.4(MET):c.1363C>A (p.Leu455Ile)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1038269|NM_000245.4(MET):c.1601C>T (p.Pro534Leu)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1038542|NM_000245.4(MET):c.3117C>G (p.Asp1039Glu)|single nucleotide variant|Uncertain significance|MET|criteria provided, multiple submitters, no conflicts|7","1038742|NM_000245.4(MET):c.2806G>A (p.Ala936Thr)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1038882|NM_000245.4(MET):c.2195A>C (p.Glu732Ala)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1039245|NM_000245.4(MET):c.874A>C (p.Met292Leu)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7","1039300|NM_000245.4(MET):c.2475G>T (p.Gly825=)|single nucleotide variant|Likely benign|MET|criteria provided, multiple submitters, no conflicts|7","1039362|NM_000245.4(MET):c.674G>T (p.Gly225Val)|single nucleotide variant|Uncertain significance|MET|criteria provided, single submitter|7"]}]}