{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":10,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:7989","source":"HGNC:7989|NRAS proto-oncogene, GTPase","targets":["1070042|NM_002524.5(NRAS):c.173C>T (p.Thr58Ile)|single nucleotide variant|Pathogenic|NRAS|reviewed by expert panel|1","13900|NM_002524.5(NRAS):c.182A>G (p.Gln61Arg)|single nucleotide variant|Pathogenic|NRAS|criteria provided, multiple submitters, no conflicts|1","13902|NM_002524.5(NRAS):c.149C>T (p.Thr50Ile)|single nucleotide variant|Pathogenic|NRAS|reviewed by expert panel|1","13903|NM_002524.5(NRAS):c.179G>A (p.Gly60Glu)|single nucleotide variant|Pathogenic|NRAS|reviewed by expert panel|1","177778|NM_002524.5(NRAS):c.34G>A (p.Gly12Ser)|single nucleotide variant|Pathogenic|NRAS|reviewed by expert panel|1","280409|NM_002524.5(NRAS):c.182A>C (p.Gln61Pro)|single nucleotide variant|Pathogenic|NRAS|criteria provided, single submitter|1","39647|NM_002524.5(NRAS):c.101C>T (p.Pro34Leu)|single nucleotide variant|Pathogenic|NRAS|no assertion criteria provided|1","40468|NM_002524.5(NRAS):c.34G>T (p.Gly12Cys)|single nucleotide variant|Pathogenic|NRAS|criteria provided, single submitter|1","40469|NM_002524.5(NRAS):c.34G>C (p.Gly12Arg)|single nucleotide variant|Pathogenic|NRAS|criteria provided, multiple submitters, no conflicts|1","40472|NM_002524.5(NRAS):c.112-1_113dup|Duplication|Pathogenic|NRAS|criteria provided, single submitter|1"]}]}