{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":4,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:4910","source":"HGNC:4910|hypoxia inducible factor 1 subunit alpha","targets":["1803802|NM_001530.4(HIF1A):c.1892G>A (p.Arg631His)|single nucleotide variant|Likely pathogenic|HIF1A|criteria provided, single submitter|14","1803803|NM_001530.4(HIF1A):c.1961C>T (p.Ala654Val)|single nucleotide variant|Likely pathogenic|HIF1A|criteria provided, single submitter|14","1803804|NM_001530.4(HIF1A):c.2075C>G (p.Ser692Cys)|single nucleotide variant|Likely pathogenic|HIF1A|criteria provided, single submitter|14","1803805|NM_001530.4(HIF1A):c.1369G>A (p.Glu457Lys)|single nucleotide variant|Likely pathogenic|HIF1A|criteria provided, single submitter|14"]}]}