{"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:3765","source":"HGNC:3765|fms related receptor tyrosine kinase 3","targets":["16270|FLT3, INTERNAL TANDEM DUP|Duplication|Pathogenic|FLT3|no assertion criteria provided|","16271|NM_004119.3(FLT3):c.2520_2521insGGATCC (p.Ser840_Asn841insGlySer)|Insertion|Pathogenic|FLT3|no assertion criteria provided|13","16272|NM_004119.3(FLT3):c.2504A>T (p.Asp835Val)|single nucleotide variant|Pathogenic|FLT3|no assertion criteria provided|13","16273|NM_004119.3(FLT3):c.2503G>C (p.Asp835His)|single nucleotide variant|Pathogenic|FLT3|no assertion criteria provided|13","16274|NM_004119.3(FLT3):c.2503G>A (p.Asp835Asn)|single nucleotide variant|Pathogenic|FLT3|no assertion criteria provided|13","16276|NM_004119.3(FLT3):c.2503G>T (p.Asp835Tyr)|single nucleotide variant|Pathogenic|FLT3|no assertion criteria provided|13","16277|NM_004119.3(FLT3):c.2503_2505del (p.Asp835del)|Deletion|Pathogenic|FLT3|no assertion criteria provided|13","16278|NM_004119.3(FLT3):c.1777_1779del (p.Asp593del)|Deletion|Pathogenic|FLT3|no assertion criteria provided|13","219096|NM_004119.3(FLT3):c.1773_1793dup (p.Tyr597_Glu598insAspValAspPheArgGluTyr)|Duplication|Pathogenic|FLT3|criteria provided, single submitter|13","375972|NM_004119.3(FLT3):c.2505T>A (p.Asp835Glu)|single nucleotide variant|Pathogenic|FLT3|no assertion criteria provided|13"]}]}