{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":37,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:6407","source":"HGNC:6407|KRAS proto-oncogene, GTPase","targets":["1172833|NM_004985.5(KRAS):c.197_198insTGACCTGCT (p.Ala66_Met67insAspLeuLeu)|Insertion|Pathogenic|KRAS|criteria provided, single submitter|12","1219824|NM_004985.5(KRAS):c.346A>C (p.Asn116His)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","12580|NM_004985.5(KRAS):c.38G>A (p.Gly13Asp)|single nucleotide variant|Pathogenic|KRAS|criteria provided, multiple submitters, no conflicts|12","12581|NM_033360.4(KRAS):c.175G>A (p.Ala59Thr)|single nucleotide variant|Pathogenic|KRAS|no assertion criteria provided|12","12583|NM_004985.5(KRAS):c.35G>T (p.Gly12Val)|single nucleotide variant|Pathogenic|KRAS|criteria provided, multiple submitters, no conflicts|12","12584|NM_004985.5(KRAS):c.34G>A (p.Gly12Ser)|single nucleotide variant|Pathogenic|KRAS|criteria provided, multiple submitters, no conflicts|12","12585|NM_033360.4(KRAS):c.27_29dup (p.Gly10dup)|Duplication|Pathogenic|KRAS|no assertion criteria provided|12","12586|NM_004985.5(KRAS):c.178G>C (p.Gly60Arg)|single nucleotide variant|Pathogenic|KRAS|reviewed by expert panel|12","12587|NM_004985.5(KRAS):c.458A>T (p.Asp153Val)|single nucleotide variant|Pathogenic|KRAS|reviewed by expert panel|12","12588|NM_004985.5(KRAS):c.173C>T (p.Thr58Ile)|single nucleotide variant|Pathogenic|KRAS|reviewed by expert panel|12","12589|NM_004985.5(KRAS):c.40G>A (p.Val14Ile)|single nucleotide variant|Pathogenic|KRAS|reviewed by expert panel|12","12591|NM_033360.4(KRAS):c.*9T>G|single nucleotide variant|Pathogenic|KRAS|no assertion criteria provided|12","12593|NM_004985.5(KRAS):c.37G>C (p.Gly13Arg)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","12594|NM_033360.4(KRAS):c.15A>T (p.Lys5Asn)|single nucleotide variant|Pathogenic|KRAS|reviewed by expert panel|12","12595|NM_033360.4(KRAS):c.*22C>G|single nucleotide variant|Pathogenic|KRAS|criteria provided, multiple submitters, no conflicts|12","12597|NM_033360.4(KRAS):c.178G>A (p.Gly60Ser)|single nucleotide variant|Pathogenic|KRAS|criteria provided, multiple submitters, no conflicts|12","163758|NM_004985.5(KRAS):c.466T>A (p.Phe156Ile)|single nucleotide variant|Pathogenic|KRAS|criteria provided, multiple submitters, no conflicts|12","1691382|NM_004985.5(KRAS):c.36_37delinsGC (p.Gly13Arg)|Indel|Pathogenic|KRAS|criteria provided, single submitter|12","1695421|NM_004985.5(KRAS):c.53C>T (p.Ala18Val)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","1695422|NM_004985.5(KRAS):c.194_195insGGCAATGAGGGACCAGTACAG (p.Tyr64_Ser65insArgAlaMetArgAspGlnTyr)|Insertion|Pathogenic|KRAS|criteria provided, single submitter|12","1701193|NM_004985.5(KRAS):c.33_34delinsCT (p.Gly12Cys)|Indel|Pathogenic|KRAS|criteria provided, single submitter|12","177777|NM_004985.5(KRAS):c.181C>A (p.Gln61Lys)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","217822|NM_004985.5(KRAS):c.57G>C (p.Leu19Phe)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","2716407|NM_004985.5(KRAS):c.467T>C (p.Phe156Ser)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","31940|NM_033360.4(KRAS):c.211T>C (p.Tyr71His)|single nucleotide variant|Pathogenic|KRAS|no assertion criteria provided|12","372705|NM_033360.4(KRAS):c.15A>C (p.Lys5Asn)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","375965|NM_033360.4(KRAS):c.351A>C (p.Lys117Asn)|single nucleotide variant|Pathogenic|KRAS|criteria provided, multiple submitters, no conflicts|12","40451|NM_033360.4(KRAS):c.64C>G (p.Gln22Glu)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","40452|NM_004985.5(KRAS):c.65A>G (p.Gln22Arg)|single nucleotide variant|Pathogenic|KRAS|reviewed by expert panel|12","40454|NM_004985.5(KRAS):c.101C>T (p.Pro34Leu)|single nucleotide variant|Pathogenic|KRAS|reviewed by expert panel|12","424018|NM_033360.4(KRAS):c.31_32insGGC (p.Ala11delinsGlyPro)|Insertion|Pathogenic|KRAS|criteria provided, single submitter|12","4279990|NM_004985.5(KRAS):c.182_183delinsGT (p.Gln61Arg)|Indel|Pathogenic|KRAS|criteria provided, single submitter|12","431103|NM_033360.4(KRAS):c.440A>G (p.Lys147Arg)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","45116|NM_004985.5(KRAS):c.182A>T (p.Gln61Leu)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","45117|NM_004985.5(KRAS):c.183A>T (p.Gln61His)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","45124|NM_004985.5(KRAS):c.38G>T (p.Gly13Val)|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12","561755|NM_033360.4(KRAS):c.*11G>A|single nucleotide variant|Pathogenic|KRAS|criteria provided, single submitter|12"]}]}