{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":6,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:7029","source":"HGNC:7029|MET proto-oncogene, receptor tyrosine kinase","targets":["13882|NM_000245.4(MET):c.3562G>T (p.Val1188Leu)|single nucleotide variant|Pathogenic|MET|no assertion criteria provided|7","13884|NM_000245.4(MET):c.3682G>A (p.Asp1228Asn)|single nucleotide variant|Pathogenic|MET|no assertion criteria provided|7","13889|NM_000245.4(MET):c.3750G>A (p.Met1250Ile)|single nucleotide variant|Pathogenic|MET|no assertion criteria provided|7","13890|NM_000245.4(MET):c.3731A>G (p.Lys1244Arg)|single nucleotide variant|Pathogenic|MET|no assertion criteria provided|7","183686|NM_000245.4(MET):c.2521T>G (p.Phe841Val)|single nucleotide variant|Pathogenic|MET|criteria provided, single submitter|7","998144|NM_000245.4(MET):c.2855del (p.Phe952fs)|Deletion|Pathogenic|MET|no assertion criteria provided|7"]}]}