{"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:8803,10,HGNC:8803,156,1]["},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:8803","source":"HGNC:8803|platelet derived growth factor receptor alpha","targets":["1000126|NM_006206.6(PDGFRA):c.308A>G (p.Asn103Ser)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1000442|NM_006206.6(PDGFRA):c.1009G>A (p.Val337Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1000708|NM_006206.6(PDGFRA):c.1369A>G (p.Asn457Asp)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1000888|NM_006206.6(PDGFRA):c.374A>C (p.Asp125Ala)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1001179|NM_006206.6(PDGFRA):c.1322C>A (p.Pro441Gln)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1002030|NM_006206.6(PDGFRA):c.541A>T (p.Thr181Ser)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1002040|NM_006206.6(PDGFRA):c.241T>G (p.Phe81Val)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1002176|NM_006206.6(PDGFRA):c.653T>C (p.Met218Thr)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1002437|NM_006206.6(PDGFRA):c.439A>G (p.Ile147Val)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1002614|NM_006206.6(PDGFRA):c.774C>G (p.Ile258Met)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1002805|NM_006206.6(PDGFRA):c.685G>C (p.Glu229Gln)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1003019|NM_006206.6(PDGFRA):c.2196G>A (p.Met732Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1003526|NM_006206.6(PDGFRA):c.818A>G (p.Tyr273Cys)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1003659|NM_006206.6(PDGFRA):c.592T>A (p.Phe198Ile)|single nucleotide variant|Conflicting classifications of pathogenicity|PDGFRA|criteria provided, conflicting classifications|4","1003959|NC_000004.11:g.(?_55133446)_(55136925_?)del|Deletion|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1003960|NC_000004.11:g.(?_55143545)_(55161473_?)dup|Duplication|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1004434|NM_006206.6(PDGFRA):c.1653+6T>C|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1004757|NM_006206.6(PDGFRA):c.3046A>G (p.Ser1016Gly)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1006034|NM_006206.6(PDGFRA):c.1949_1955del (p.His650fs)|Deletion|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1006203|NM_006206.6(PDGFRA):c.2768G>A (p.Ser923Asn)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1006898|NM_006206.6(PDGFRA):c.1694T>C (p.Ile565Thr)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1006998|NM_006206.6(PDGFRA):c.2902G>A (p.Asp968Asn)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1007164|NM_006206.6(PDGFRA):c.2765C>T (p.Thr922Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1007897|NM_006206.6(PDGFRA):c.502G>A (p.Val168Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1007912|NM_006206.6(PDGFRA):c.3157G>A (p.Gly1053Ser)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1007915|NM_006206.6(PDGFRA):c.2844G>C (p.Glu948Asp)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1008045|NM_006206.6(PDGFRA):c.2315C>A (p.Ser772Tyr)|single nucleotide variant|Conflicting classifications of pathogenicity|PDGFRA|criteria provided, conflicting classifications|4","1008437|NM_006206.6(PDGFRA):c.1661G>T (p.Arg554Met)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1009007|NM_006206.6(PDGFRA):c.1787-6C>A|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1009850|NM_006206.6(PDGFRA):c.2207A>C (p.Gln736Pro)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1009933|NM_006206.6(PDGFRA):c.1331A>T (p.Asp444Val)|single nucleotide variant|Conflicting classifications of pathogenicity|PDGFRA|criteria provided, conflicting classifications|4","1010094|NM_006206.6(PDGFRA):c.2980A>T (p.Lys994Ter)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1010276|NM_006206.6(PDGFRA):c.1015G>A (p.Val339Met)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1010915|NM_006206.6(PDGFRA):c.1009G>T (p.Val337Leu)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1011099|NM_006206.6(PDGFRA):c.1622C>T (p.Ser541Leu)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1011132|NM_006206.6(PDGFRA):c.767A>G (p.Lys256Arg)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1011140|NM_006206.6(PDGFRA):c.673T>C (p.Tyr225His)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1011169|NM_006206.6(PDGFRA):c.3161C>G (p.Ser1054Cys)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1011568|NM_006206.6(PDGFRA):c.2788G>T (p.Val930Leu)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1011804|NM_006206.6(PDGFRA):c.3091G>A (p.Glu1031Lys)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1011927|NM_006206.6(PDGFRA):c.2851G>C (p.Glu951Gln)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1013672|NM_006206.6(PDGFRA):c.1279T>C (p.Ser427Pro)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1014076|NM_006206.6(PDGFRA):c.1217C>T (p.Thr406Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1014209|NM_006206.6(PDGFRA):c.979G>C (p.Val327Leu)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1014308|NM_006206.6(PDGFRA):c.1704T>G (p.Asp568Glu)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1014775|NM_006206.6(PDGFRA):c.928C>T (p.His310Tyr)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1015136|NM_006206.6(PDGFRA):c.2002+1G>A|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1015690|NM_006206.6(PDGFRA):c.2276G>C (p.Arg759Thr)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1015702|NM_006206.6(PDGFRA):c.1237+3A>G|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1016053|NM_006206.6(PDGFRA):c.244G>T (p.Val82Leu)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1016125|NM_006206.6(PDGFRA):c.40C>A (p.Leu14Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1016462|NM_006206.6(PDGFRA):c.984C>A (p.Asn328Lys)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1017616|NM_006206.6(PDGFRA):c.2675-1G>A|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1017753|NM_006206.6(PDGFRA):c.468G>C (p.Glu156Asp)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1018304|NM_006206.6(PDGFRA):c.424G>A (p.Asp142Asn)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1018595|NM_006206.6(PDGFRA):c.629-3T>C|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1018613|NM_006206.6(PDGFRA):c.3041C>T (p.Ala1014Val)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1018819|NM_006206.6(PDGFRA):c.2909T>A (p.Leu970Gln)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1018986|NM_006206.6(PDGFRA):c.575C>G (p.Thr192Ser)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1019256|NM_006206.6(PDGFRA):c.3104G>A (p.Gly1035Asp)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1019387|NM_006206.6(PDGFRA):c.1772A>G (p.Asp591Gly)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1019501|NM_006206.6(PDGFRA):c.3237C>A (p.Asp1079Glu)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1019626|NM_006206.6(PDGFRA):c.2266G>T (p.Asp756Tyr)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1019988|NM_006206.6(PDGFRA):c.796G>A (p.Val266Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1021611|NM_006206.6(PDGFRA):c.1038G>T (p.Arg346Ser)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1022155|NM_006206.6(PDGFRA):c.1618A>T (p.Ile540Phe)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1022361|NM_006206.6(PDGFRA):c.2067T>G (p.Asn689Lys)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1022371|NM_006206.6(PDGFRA):c.182T>C (p.Met61Thr)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1022872|NM_006206.6(PDGFRA):c.2156+3G>T|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1023059|NM_006206.6(PDGFRA):c.1431C>G (p.His477Gln)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1023105|NM_006206.6(PDGFRA):c.198C>G (p.Ser66Arg)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1023274|NM_006206.6(PDGFRA):c.2606_2610dup (p.Leu871fs)|Duplication|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1023557|NM_006206.6(PDGFRA):c.1122-7T>A|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1023579|NM_006206.6(PDGFRA):c.1591G>A (p.Val531Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1024334|NM_006206.6(PDGFRA):c.1866G>A (p.Met622Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1024360|NM_006206.6(PDGFRA):c.3173C>T (p.Thr1058Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1024371|NM_006206.6(PDGFRA):c.768dup (p.Gly257fs)|Duplication|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1024705|NM_006206.6(PDGFRA):c.3221_3222delinsCC (p.Asp1074Ala)|Indel|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1025233|NM_006206.6(PDGFRA):c.2992G>C (p.Asp998His)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1025421|NM_006206.6(PDGFRA):c.278C>A (p.Ala93Asp)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1026088|NM_006206.6(PDGFRA):c.2880G>C (p.Lys960Asn)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1026609|NM_006206.6(PDGFRA):c.1264G>C (p.Asp422His)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1034780|NM_006206.6(PDGFRA):c.1755A>G (p.Arg585=)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1034974|NM_006206.6(PDGFRA):c.933G>C (p.Glu311Asp)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1035452|NM_006206.6(PDGFRA):c.1792G>A (p.Val598Ile)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1035525|NM_006206.6(PDGFRA):c.1090A>G (p.Thr364Ala)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1035742|NM_006206.6(PDGFRA):c.1519C>T (p.Leu507Phe)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1036092|NM_006206.6(PDGFRA):c.35G>C (p.Gly12Ala)|single nucleotide variant|Conflicting classifications of pathogenicity|PDGFRA|criteria provided, conflicting classifications|4","1036196|NM_006206.6(PDGFRA):c.2792A>C (p.Lys931Thr)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1036572|NM_006206.6(PDGFRA):c.3079C>T (p.Pro1027Ser)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1037490|NM_006206.6(PDGFRA):c.319A>T (p.Thr107Ser)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1037517|NM_006206.6(PDGFRA):c.2159A>G (p.Tyr720Cys)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1037819|NM_006206.6(PDGFRA):c.993A>T (p.Glu331Asp)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1037865|NM_006206.6(PDGFRA):c.89T>C (p.Ile30Thr)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1038558|NM_006206.6(PDGFRA):c.976G>A (p.Ala326Thr)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1039290|NM_006206.6(PDGFRA):c.1462G>A (p.Val488Met)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1039423|NM_006206.6(PDGFRA):c.560A>G (p.Tyr187Cys)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1039691|NM_006206.6(PDGFRA):c.1288G>A (p.Gly430Arg)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1040313|NM_006206.6(PDGFRA):c.208G>A (p.Glu70Lys)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, single submitter|4","1041781|NM_006206.6(PDGFRA):c.1474A>C (p.Lys492Gln)|single nucleotide variant|Uncertain significance|PDGFRA|criteria provided, multiple submitters, no conflicts|4"]}]}