{"context":{"query":">>hgnc>>clinvar[germline_classification==\"Pathogenic\"]","source_dataset":"hgnc","target_dataset":"clinvar"},"stats":{"queried":1,"total":12,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"HGNC:76","source":"HGNC:76|ABL proto-oncogene 1, non-receptor tyrosine kinase","targets":["1184856|NM_005157.6(ABL1):c.1388G>A (p.Gly463Asp)|single nucleotide variant|Pathogenic|ABL1|criteria provided, single submitter|9","12625|NM_005157.6(ABL1):c.707A>T (p.Glu236Val)|single nucleotide variant|Pathogenic|ABL1|no assertion criteria provided|9","12626|NM_005157.6(ABL1):c.706G>A (p.Glu236Lys)|single nucleotide variant|Pathogenic|ABL1|no assertion criteria provided|9","12627|NM_005157.6(ABL1):c.757T>C (p.Tyr253His)|single nucleotide variant|Pathogenic|ABL1|no assertion criteria provided|9","12628|NM_005157.6(ABL1):c.931T>C (p.Phe311Leu)|single nucleotide variant|Pathogenic|ABL1|no assertion criteria provided|9","12629|NM_005157.6(ABL1):c.1052T>C (p.Met351Thr)|single nucleotide variant|Pathogenic|ABL1|no assertion criteria provided|9","3063094|GRCh37/hg19 9q34.11-34.13(chr9:131815597-134209182)x1|copy number loss|Pathogenic|ABL1|criteria provided, single submitter|9","374794|NM_005157.6(ABL1):c.1009G>A (p.Ala337Thr)|single nucleotide variant|Pathogenic|ABL1|criteria provided, multiple submitters, no conflicts|9","376084|NM_005157.6(ABL1):c.730A>G (p.Met244Val)|single nucleotide variant|Pathogenic|ABL1|criteria provided, single submitter|9","376091|NM_005157.6(ABL1):c.764A>T (p.Glu255Val)|single nucleotide variant|Pathogenic|ABL1|no assertion criteria provided|9","376097|NM_005157.6(ABL1):c.1187A>G (p.His396Arg)|single nucleotide variant|Pathogenic|ABL1|no assertion criteria provided|9","617566|Single allele|Translocation|Pathogenic|ABL1|no assertion criteria provided|9"]}]}