{"context":{"query":">>hgnc>>clinvar","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":29,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:17635","source":"HGNC:17635|CD274 molecule","targets":["1251725|NM_014143.4(CD274):c.*93G>A|single nucleotide variant|Benign|CD274|criteria provided, multiple submitters, no conflicts|9","1251890|NM_014143.4(CD274):c.*2635A>G|single nucleotide variant|Benign|CD274|criteria provided, multiple submitters, no conflicts|9","1274128|NC_000009.12:g.5450497G>C|single nucleotide variant|Benign|CD274|criteria provided, multiple submitters, no conflicts|9","1696626|Single allele|Duplication|Uncertain significance|CD274|criteria provided, single submitter|9","1703576|GRCh37/hg19 9p24.3-q13(chr9:203861-68342786)|copy number gain|Pathogenic|CD274|no assertion criteria provided|9","1706515|GRCh37/hg19 9p24.3-23(chr9:203861-10283912)x1|copy number loss|Pathogenic|CD274|no assertion criteria provided|9","2208831|NM_014143.4(CD274):c.548A>C (p.Asn183Thr)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","2307554|NM_014143.4(CD274):c.829A>G (p.Thr277Ala)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","2659049|NM_014143.4(CD274):c.437C>G (p.Pro146Arg)|single nucleotide variant|Likely benign|CD274|criteria provided, single submitter|9","2684571|GRCh37/hg19 9p24.1(chr9:5174638-5722779)x3|copy number gain|Uncertain significance|CD274|criteria provided, single submitter|9","3140479|NM_014143.4(CD274):c.649G>A (p.Glu217Lys)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","3264788|NM_014143.4(CD274):c.436C>A (p.Pro146Thr)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","3906943|CD274, IVS4DS, G-A, +1|single nucleotide variant|Pathogenic|CD274|no assertion criteria provided|","3998154|NM_014143.4(CD274):c.558A>C (p.Arg186Ser)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","3998155|NM_014143.4(CD274):c.832A>C (p.Asn278His)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","3998156|NM_014143.4(CD274):c.343A>G (p.Met115Val)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","4222761|NM_014143.4(CD274):c.615G>C (p.Glu205Asp)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","4222762|NM_014143.4(CD274):c.61G>A (p.Val21Ile)|single nucleotide variant|Likely benign|CD274|criteria provided, single submitter|9","4356905|NM_014143.4(CD274):c.66G>A (p.Thr22=)|single nucleotide variant||CD274||9","4356906|NM_014143.4(CD274):c.534G>C (p.Lys178Asn)|single nucleotide variant||CD274||9","4356907|NM_014143.4(CD274):c.790G>C (p.Gly264Arg)|single nucleotide variant||CD274||9","442671|GRCh37/hg19 9p24.3-23(chr9:203861-13486759)x1|copy number loss|Pathogenic|CD274|no assertion criteria provided|9","4539645|NM_014143.4(CD274):c.682+1G>A|single nucleotide variant||CD274||9","4650550|NM_014143.4(CD274):c.545C>T (p.Thr182Ile)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","4650551|NM_014143.4(CD274):c.526A>T (p.Ser176Cys)|single nucleotide variant|Uncertain significance|CD274|criteria provided, single submitter|9","563686|GRCh37/hg19 9p24.3-q21.11(chr9:203861-70985795)x4|copy number gain|Pathogenic|CD274|no assertion criteria provided|9","57439|GRCh38/hg38 9p24.1(chr9:4970093-5483250)x1|copy number loss|Uncertain significance|CD274|criteria provided, single submitter|9","738348|NM_014143.4(CD274):c.363C>A (p.Ala121=)|single nucleotide variant|Benign|CD274|criteria provided, single submitter|9","792122|NM_014143.4(CD274):c.198A>G (p.Gln66=)|single nucleotide variant|Benign|CD274|criteria provided, single submitter|9"]}]}