{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":50,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:1582","source":"HGNC:1582|cyclin D1","targets":["1227388|NM_053056.3(CCND1):c.575-120G>A|single nucleotide variant|Benign|CCND1|criteria provided, multiple submitters, no conflicts|11","1232882|NM_053056.3(CCND1):c.*65C>A|single nucleotide variant|Benign|CCND1|criteria provided, multiple submitters, no conflicts|11","1241350|NM_053056.3(CCND1):c.724-205A>G|single nucleotide variant|Benign|CCND1|criteria provided, multiple submitters, no conflicts|11","1250573|NM_053056.3(CCND1):c.669C>T (p.Phe223=)|single nucleotide variant|Benign|CCND1|criteria provided, multiple submitters, no conflicts|11","1283485|NM_053056.3(CCND1):c.724-26A>G|single nucleotide variant|Benign|CCND1|criteria provided, multiple submitters, no conflicts|11","1286069|NM_053056.3(CCND1):c.415-170G>C|single nucleotide variant|Benign|CCND1|criteria provided, multiple submitters, no conflicts|11","1340503|GRCh37/hg19 11q13.3(chr11:69233407-69475789)x3|copy number gain|Uncertain significance|CCND1|no assertion criteria provided|11","13755|NM_053056.3(CCND1):c.723G>A (p.Pro241=)|single nucleotide variant|Benign|CCND1|criteria provided, multiple submitters, no conflicts|11","2297468|NM_053056.3(CCND1):c.785C>T (p.Ala262Val)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","2299476|NM_053056.3(CCND1):c.691C>G (p.Arg231Gly)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","2341922|NM_053056.3(CCND1):c.868G>A (p.Val290Met)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","2391496|NM_053056.3(CCND1):c.800A>G (p.Asp267Gly)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","2489951|NM_053056.3(CCND1):c.569C>T (p.Ala190Val)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","2554042|NM_053056.3(CCND1):c.753C>G (p.Ile251Met)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","2581321|NM_053056.3(CCND1):c.387_392delinsGGAG (p.Asp129fs)|Indel|Uncertain significance|CCND1|criteria provided, single submitter|11","2610543|NM_053056.3(CCND1):c.560C>T (p.Ala187Val)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","2642049|NM_053056.3(CCND1):c.*771C>T|single nucleotide variant|Likely benign|CCND1|criteria provided, single submitter|11","3034107|NM_053056.3(CCND1):c.649C>T (p.Leu217=)|single nucleotide variant|Likely benign|CCND1|no assertion criteria provided|11","3038710|NM_053056.3(CCND1):c.827AGG[4] (p.Glu280del)|Microsatellite|Likely benign|CCND1|no assertion criteria provided|11","3050562|NM_053056.3(CCND1):c.714G>A (p.Lys238=)|single nucleotide variant|Likely benign|CCND1|no assertion criteria provided|11","3139896|NM_053056.3(CCND1):c.557T>C (p.Val186Ala)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","3139897|NM_053056.3(CCND1):c.689C>T (p.Thr230Ile)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","3257949|NM_053056.3(CCND1):c.136A>G (p.Lys46Glu)|single nucleotide variant||CCND1||11","3264539|NM_053056.3(CCND1):c.643C>G (p.Leu215Val)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","3358898|NM_053056.3(CCND1):c.76C>T (p.Arg26Trp)|single nucleotide variant|Uncertain significance|CCND1|no assertion criteria provided|11","3487396|NM_053056.3(CCND1):c.882C>A (p.Asp294Glu)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","3573959|NM_053056.3(CCND1):c.198+4C>T|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","3764887|NM_053056.3(CCND1):c.131A>C (p.Tyr44Ser)|single nucleotide variant||CCND1||11","3829082|NM_053056.3(CCND1):c.332C>T (p.Ser111Phe)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","3997604|NM_053056.3(CCND1):c.658C>T (p.Pro220Ser)|single nucleotide variant|Likely benign|CCND1|criteria provided, single submitter|11","4222058|NM_053056.3(CCND1):c.797T>C (p.Met266Thr)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","4283773|NM_053056.3(CCND1):c.724-13CT[4]|Microsatellite||CCND1||11","4375944|NM_053056.3(CCND1):c.138A>G (p.Lys46=)|single nucleotide variant||CCND1||11","4375945|NM_053056.3(CCND1):c.324C>A (p.Phe108Leu)|single nucleotide variant||CCND1||11","4375946|NM_053056.3(CCND1):c.414+63G>T|single nucleotide variant||CCND1||11","4375947|NM_053056.3(CCND1):c.414+160C>T|single nucleotide variant||CCND1||11","4375949|NM_053056.3(CCND1):c.415-170G>T|single nucleotide variant||CCND1||11","4375950|NM_053056.3(CCND1):c.415-1G>A|single nucleotide variant||CCND1||11","4375951|NM_053056.3(CCND1):c.574G>T (p.Asp192Tyr)|single nucleotide variant||CCND1||11","4375952|NM_053056.3(CCND1):c.575-243G>T|single nucleotide variant||CCND1||11","4375953|NM_053056.3(CCND1):c.723G>C (p.Pro241=)|single nucleotide variant||CCND1||11","4375954|NM_053056.3(CCND1):c.723G>T (p.Pro241=)|single nucleotide variant||CCND1||11","4375955|NM_053056.3(CCND1):c.*1824T>G|single nucleotide variant||CCND1||11","4375956|NM_053056.3(CCND1):c.*2067A>G|single nucleotide variant||CCND1||11","442080|GRCh37/hg19 11q13.2-13.4(chr11:67799160-70701268)x1|copy number loss|Likely pathogenic|CCND1|no assertion criteria provided|11","4650033|NM_053056.3(CCND1):c.700T>A (p.Ser234Thr)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","4650034|NM_053056.3(CCND1):c.235C>T (p.Pro79Ser)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","4650036|NM_053056.3(CCND1):c.467C>T (p.Thr156Ile)|single nucleotide variant|Uncertain significance|CCND1|criteria provided, single submitter|11","736722|NM_053056.3(CCND1):c.735G>A (p.Arg245=)|single nucleotide variant|Benign/Likely benign|CCND1|criteria provided, multiple submitters, no conflicts|11","761360|NM_053056.3(CCND1):c.180C>G (p.Val60=)|single nucleotide variant|Likely benign|CCND1|criteria provided, single submitter|11"]}]}