{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":48,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:8760","source":"HGNC:8760|programmed cell death 1","targets":["1177788|NM_005018.3(PDCD1):c.76+15C>T|single nucleotide variant|Benign|PDCD1|criteria provided, multiple submitters, no conflicts|2","1226460|NM_005018.3(PDCD1):c.804T>C (p.Ala268=)|single nucleotide variant|Benign|PDCD1|criteria provided, multiple submitters, no conflicts|2","1233776|NM_005018.3(PDCD1):c.437-115G>A|single nucleotide variant|Benign|PDCD1|criteria provided, multiple submitters, no conflicts|2","1234595|NM_005018.3(PDCD1):c.76+241_76+242insTTTGGGCAGGTGACTGCCCAAAG|Insertion|Benign|PDCD1|criteria provided, single submitter|2","1251704|NM_005018.3(PDCD1):c.593-61dup|Duplication|Benign|PDCD1|criteria provided, single submitter|2","1252837|NM_005018.3(PDCD1):c.77-287del|Deletion|Benign|PDCD1|criteria provided, single submitter|2","1255049|NM_005018.3(PDCD1):c.*889G>A|single nucleotide variant|Benign|PDCD1|criteria provided, multiple submitters, no conflicts|2","1257448|NM_005018.3(PDCD1):c.628-110A>G|single nucleotide variant|Benign|PDCD1|criteria provided, multiple submitters, no conflicts|2","1258165|NM_005018.3(PDCD1):c.76+126G>C|single nucleotide variant|Benign|PDCD1|criteria provided, multiple submitters, no conflicts|2","1260387|NM_005018.3(PDCD1):c.593-56C>G|single nucleotide variant|Benign|PDCD1|criteria provided, multiple submitters, no conflicts|2","1265148|NM_005018.3(PDCD1):c.627+189G>A|single nucleotide variant|Benign|PDCD1|criteria provided, multiple submitters, no conflicts|2","1270664|NM_005018.3(PDCD1):c.627+252C>T|single nucleotide variant|Benign|PDCD1|criteria provided, single submitter|2","1276991|NM_005018.3(PDCD1):c.77-180G>C|single nucleotide variant|Benign|PDCD1|criteria provided, single submitter|2","1282693|NM_005018.3(PDCD1):c.644C>T (p.Ala215Val)|single nucleotide variant|Benign|PDCD1|criteria provided, multiple submitters, no conflicts|2","1286750|NM_005018.3(PDCD1):c.77-218T>C|single nucleotide variant|Benign|PDCD1|criteria provided, single submitter|2","2243463|NM_005018.3(PDCD1):c.38C>T (p.Ala13Val)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","2333454|NM_005018.3(PDCD1):c.347A>T (p.Asn116Ile)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","2372384|NM_005018.3(PDCD1):c.31G>A (p.Val11Ile)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","2398088|NM_005018.3(PDCD1):c.581G>A (p.Arg194Gln)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","2531224|NM_005018.3(PDCD1):c.344G>A (p.Arg115His)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","3026042|NM_005018.3(PDCD1):c.804T>G (p.Ala268=)|single nucleotide variant|Likely benign|PDCD1|criteria provided, single submitter|2","3039619|NM_005018.3(PDCD1):c.437-8C>T|single nucleotide variant|Likely benign|PDCD1|no assertion criteria provided|2","3042975|NM_005018.3(PDCD1):c.436+10C>T|single nucleotide variant|Likely benign|PDCD1|no assertion criteria provided|2","3045064|NM_005018.3(PDCD1):c.480C>G (p.Pro160=)|single nucleotide variant|Likely benign|PDCD1|no assertion criteria provided|2","3210522|NM_005018.3(PDCD1):c.633G>T (p.Glu211Asp)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","3305293|NM_005018.3(PDCD1):c.416G>A (p.Arg139Gln)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","3376502|PDCD1, 1-BP DUP, 105C|Duplication|Pathogenic|PDCD1|no assertion criteria provided|","3416048|NM_005018.3(PDCD1):c.815G>A (p.Arg272Gln)|single nucleotide variant|Likely benign|PDCD1|criteria provided, single submitter|2","3887099|NM_005018.3(PDCD1):c.341G>A (p.Arg114Gln)|single nucleotide variant|Likely benign|PDCD1|criteria provided, single submitter|2","3887101|NM_005018.3(PDCD1):c.328G>A (p.Val110Met)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","3929843|NM_005018.3(PDCD1):c.512T>C (p.Val171Ala)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","4133549|NM_005018.3(PDCD1):c.526G>T (p.Gly176Cys)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","4511939|NM_005018.3(PDCD1):c.*339G>A|single nucleotide variant||PDCD1||2","4511940|NM_005018.3(PDCD1):c.628-1G>C|single nucleotide variant||PDCD1||2","4511941|NM_005018.3(PDCD1):c.627+295A>G|single nucleotide variant||PDCD1||2","4511942|NM_005018.3(PDCD1):c.627+254C>T|single nucleotide variant||PDCD1||2","4511943|NM_005018.3(PDCD1):c.593-99G>C|single nucleotide variant||PDCD1||2","4511944|NM_005018.3(PDCD1):c.157A>T (p.Thr53Ser)|single nucleotide variant||PDCD1||2","4511945|NM_005018.3(PDCD1):c.76+125C>T|single nucleotide variant||PDCD1||2","4511946|NM_005018.3(PDCD1):c.76+13G>A|single nucleotide variant||PDCD1||2","4511947|NM_005018.3(PDCD1):c.-27C>T|single nucleotide variant||PDCD1||2","4534800|NM_005018.3(PDCD1):c.321C>T (p.His107=)|single nucleotide variant|Likely benign|PDCD1|criteria provided, single submitter|2","4566153|NM_005018.3(PDCD1):c.854C>T (p.Ser285Phe)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","4566154|NM_005018.3(PDCD1):c.415C>T (p.Arg139Trp)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","4566155|NM_005018.3(PDCD1):c.256C>T (p.Arg86Cys)|single nucleotide variant|Uncertain significance|PDCD1|criteria provided, single submitter|2","624557|GRCh37/hg19 2q37.3(chr2:242766297-242886445)x3|copy number gain|Uncertain significance|PDCD1|criteria provided, single submitter|2","790522|NM_005018.3(PDCD1):c.76+10G>A|single nucleotide variant|Benign|PDCD1|criteria provided, single submitter|2","9251|NM_005018.3(PDCD1):c.627+189G>C|single nucleotide variant|Benign|PDCD1|no assertion criteria provided|2"]}]}