{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely 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":["1320232|NM_002524.5(NRAS):c.449A>G (p.Gln150Arg)|single nucleotide variant|Likely pathogenic|NRAS|criteria provided, single submitter|1","1335888|NM_002524.5(NRAS):c.108A>G (p.Ile36Met)|single nucleotide variant|Likely pathogenic|NRAS|criteria provided, single submitter|1","13899|NM_002524.5(NRAS):c.37G>C (p.Gly13Arg)|single nucleotide variant|Likely pathogenic|NRAS|criteria provided, multiple submitters, no conflicts|1","222971|NM_002524.5(NRAS):c.71T>A (p.Ile24Asn)|single nucleotide variant|Likely pathogenic|NRAS|reviewed by expert panel|1","2672090|NM_002524.5(NRAS):c.191_196dup (p.Ser65_Ala66insAspSer)|Duplication|Likely pathogenic|NRAS|criteria provided, single submitter|1","3029607|NM_002524.5(NRAS):c.34_35delinsTT (p.Gly12Phe)|Indel|Likely pathogenic|NRAS|no assertion criteria provided|1","375876|NM_002524.5(NRAS):c.38G>T (p.Gly13Val)|single nucleotide variant|Likely pathogenic|NRAS|criteria provided, single submitter|1","561786|NM_002524.5(NRAS):c.178G>A (p.Gly60Arg)|single nucleotide variant|Likely pathogenic|NRAS|criteria provided, multiple submitters, no conflicts|1","812886|NM_002524.5(NRAS):c.176C>A (p.Ala59Asp)|single nucleotide variant|Likely pathogenic|NRAS|no assertion criteria provided|1","981556|NM_002524.5(NRAS):c.204A>T (p.Arg68Ser)|single nucleotide variant|Likely pathogenic|NRAS|no assertion criteria provided|1"]}]}