{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Likely pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":7,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:427","source":"HGNC:427|ALK receptor tyrosine kinase","targets":["1705031|NM_004304.5(ALK):c.3538G>C (p.Val1180Leu)|single nucleotide variant|Likely pathogenic|ALK|no assertion criteria provided|2","217854|NM_004304.5(ALK):c.3718T>G (p.Leu1240Val)|single nucleotide variant|Likely pathogenic|ALK|no assertion criteria provided|2","2445401|NM_004304.5(ALK):c.402G>C (p.Lys134Asn)|single nucleotide variant|Likely pathogenic|ALK|criteria provided, single submitter|2","375887|NM_004304.5(ALK):c.3521T>G (p.Phe1174Cys)|single nucleotide variant|Likely pathogenic|ALK|criteria provided, single submitter|2","376135|NM_004304.5(ALK):c.3586C>A (p.Leu1196Met)|single nucleotide variant|Likely pathogenic|ALK|no assertion criteria provided|2","547174|inv(2)(p21p23.2)|Inversion|Likely pathogenic|ALK|no assertion criteria provided|2","978809|NM_004304.5(ALK):c.4298_4299del (p.Glu1433fs)|Deletion|Likely pathogenic|ALK|no assertion criteria provided|2"]}]}