{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely benign\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]HGNC:8803,10,HGNC:8803,168,5]["},"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":["1023557|NM_006206.6(PDGFRA):c.1122-7T>A|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1054747|NM_006206.6(PDGFRA):c.633A>G (p.Thr211=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1061027|NM_006206.6(PDGFRA):c.465C>A (p.Pro155=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1077419|NM_006206.6(PDGFRA):c.1892-7T>C|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1078670|NM_006206.6(PDGFRA):c.2502C>T (p.Ile834=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1078739|NM_006206.6(PDGFRA):c.2898C>T (p.His966=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1079259|NM_006206.6(PDGFRA):c.1065T>C (p.Thr355=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1079412|NM_006206.6(PDGFRA):c.2067T>C (p.Asn689=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1079766|NM_006206.6(PDGFRA):c.1335T>C (p.Ile445=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1079981|NM_006206.6(PDGFRA):c.2664C>A (p.Ile888=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1080842|NM_006206.6(PDGFRA):c.1365-7T>C|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1082029|NM_006206.6(PDGFRA):c.537T>C (p.Asn179=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1082640|NM_006206.6(PDGFRA):c.3099C>T (p.Asp1033=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1082645|NM_006206.6(PDGFRA):c.1410A>C (p.Ser470=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1082649|NM_006206.6(PDGFRA):c.3126G>T (p.Ser1042=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1083935|NM_006206.6(PDGFRA):c.615T>C (p.Val205=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1084213|NM_006206.6(PDGFRA):c.333G>A (p.Glu111=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1084215|NM_006206.6(PDGFRA):c.582A>G (p.Lys194=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1084351|NM_006206.6(PDGFRA):c.2823C>T (p.Pro941=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1084662|NM_006206.6(PDGFRA):c.1302G>A (p.Arg434=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1084866|NM_006206.6(PDGFRA):c.735T>C (p.Leu245=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1084973|NM_006206.6(PDGFRA):c.84C>G (p.Pro28=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1085477|NM_006206.6(PDGFRA):c.129A>G (p.Ser43=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1085784|NM_006206.6(PDGFRA):c.2003-5C>T|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1085897|NM_006206.6(PDGFRA):c.1779A>G (p.Leu593=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1086110|NM_006206.6(PDGFRA):c.1851G>C (p.Arg617=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1087203|NM_006206.6(PDGFRA):c.249G>T (p.Thr83=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1087238|NM_006206.6(PDGFRA):c.1978T>C (p.Leu660=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1087318|NM_006206.6(PDGFRA):c.1044C>T (p.Ser348=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1087534|NM_006206.6(PDGFRA):c.2301A>G (p.Ser767=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1087859|NM_006206.6(PDGFRA):c.1653+8T>C|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1088330|NM_006206.6(PDGFRA):c.1773T>C (p.Asp591=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1088356|NM_006206.6(PDGFRA):c.1920T>C (p.Ala640=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1090355|NM_006206.6(PDGFRA):c.2025G>A (p.Glu675=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1091613|NM_006206.6(PDGFRA):c.267T>C (p.Ser89=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1091807|NM_006206.6(PDGFRA):c.1887A>G (p.Leu629=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1092119|NM_006206.6(PDGFRA):c.636A>G (p.Ser212=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1092546|NM_006206.6(PDGFRA):c.804C>T (p.Ser268=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1092675|NM_006206.6(PDGFRA):c.1393T>C (p.Leu465=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1094156|NM_006206.6(PDGFRA):c.3122+9G>A|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1094444|NM_006206.6(PDGFRA):c.2358C>T (p.Asn786=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1095052|NM_006206.6(PDGFRA):c.765C>A (p.Gly255=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1095228|NM_006206.6(PDGFRA):c.2675-8G>C|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1096775|NM_006206.6(PDGFRA):c.1364+9A>G|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1097545|NM_006206.6(PDGFRA):c.1635G>C (p.Leu545=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1097714|NM_006206.6(PDGFRA):c.932-6G>A|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1097986|NM_006206.6(PDGFRA):c.1491C>T (p.Ile497=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1098069|NM_006206.6(PDGFRA):c.1128A>T (p.Arg376=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1098139|NM_006206.6(PDGFRA):c.1788T>C (p.Gly596=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1098161|NM_006206.6(PDGFRA):c.1854C>T (p.Ser618=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1099158|NM_006206.6(PDGFRA):c.2835C>T (p.His945=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1099270|NM_006206.6(PDGFRA):c.1281A>C (p.Ser427=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1099365|NM_006206.6(PDGFRA):c.984C>T (p.Asn328=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1100100|NM_006206.6(PDGFRA):c.2457G>T (p.Leu819=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1100513|NM_006206.6(PDGFRA):c.2002+8C>T|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1100771|NM_006206.6(PDGFRA):c.1059T>C (p.Asn353=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1100877|NM_006206.6(PDGFRA):c.759+8C>T|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1100894|NM_006206.6(PDGFRA):c.147C>T (p.Cys49=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1100908|NM_006206.6(PDGFRA):c.921T>A (p.Ile307=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1101183|NM_006206.6(PDGFRA):c.1296G>C (p.Thr432=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1101951|NM_006206.6(PDGFRA):c.2003-8C>T|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1102458|NM_006206.6(PDGFRA):c.2763T>C (p.Ala921=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1103025|NM_006206.6(PDGFRA):c.69C>T (p.Cys23=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1103294|NM_006206.6(PDGFRA):c.3171C>T (p.Ser1057=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1103444|NM_006206.6(PDGFRA):c.429T>C (p.Asp143=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1103886|NM_006206.6(PDGFRA):c.2373T>A (p.Thr791=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1103887|NM_006206.6(PDGFRA):c.3123-10C>T|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1104048|NM_006206.6(PDGFRA):c.2650C>T (p.Leu884=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1104238|NM_006206.6(PDGFRA):c.1365-6C>T|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1104548|NM_006206.6(PDGFRA):c.1146C>T (p.Ile382=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1104591|NM_006206.6(PDGFRA):c.1017G>T (p.Val339=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1105509|NM_006206.6(PDGFRA):c.1678A>C (p.Arg560=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1106498|NM_006206.6(PDGFRA):c.2193C>T (p.Tyr731=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1106621|NM_006206.6(PDGFRA):c.629-4A>T|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1106638|NM_006206.6(PDGFRA):c.93T>G (p.Leu31=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1107462|NM_006206.6(PDGFRA):c.2976C>A (p.Thr992=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1107673|NM_006206.6(PDGFRA):c.1011A>G (p.Val337=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1109093|NM_006206.6(PDGFRA):c.1365-4C>T|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1109546|NM_006206.6(PDGFRA):c.1185A>G (p.Val395=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1111526|NM_006206.6(PDGFRA):c.1560C>G (p.Thr520=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1111702|NM_006206.6(PDGFRA):c.2130G>A (p.Leu710=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1113305|NM_006206.6(PDGFRA):c.2003-5del|Deletion|Likely benign|PDGFRA|criteria provided, single submitter|4","1113460|NM_006206.6(PDGFRA):c.1362G>A (p.Lys454=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1113649|NM_006206.6(PDGFRA):c.1770A>G (p.Arg590=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1114079|NM_006206.6(PDGFRA):c.1959A>T (p.Pro653=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1114772|NM_006206.6(PDGFRA):c.117G>A (p.Val39=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1114889|NM_006206.6(PDGFRA):c.3012G>A (p.Glu1004=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1115416|NM_006206.6(PDGFRA):c.2496G>C (p.Val832=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1115439|NM_006206.6(PDGFRA):c.1119A>C (p.Ile373=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1115793|NM_006206.6(PDGFRA):c.2151A>G (p.Thr717=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1116226|NM_006206.6(PDGFRA):c.1238-8T>C|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1116763|NM_006206.6(PDGFRA):c.1464G>T (p.Val488=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1116921|NM_006206.6(PDGFRA):c.1791G>A (p.Arg597=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1116947|NM_006206.6(PDGFRA):c.1851G>A (p.Arg617=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1117047|NM_006206.6(PDGFRA):c.1929T>G (p.Ser643=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1117553|NM_006206.6(PDGFRA):c.846G>A (p.Val282=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1118120|NM_006206.6(PDGFRA):c.1509T>C (p.Ala503=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4","1118122|NM_006206.6(PDGFRA):c.2775-9del|Deletion|Likely benign|PDGFRA|criteria provided, single submitter|4","1118143|NM_006206.6(PDGFRA):c.1323G>T (p.Pro441=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, multiple submitters, no conflicts|4","1118628|NM_006206.6(PDGFRA):c.2520C>G (p.Ala840=)|single nucleotide variant|Likely benign|PDGFRA|criteria provided, single submitter|4"]}]}