{"context":{"query":">>mondo>>clinvar","source_dataset":"mondo","target_dataset":"clinvar"},"stats":{"queried":1,"total":13,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"MONDO:0018908","source":"MONDO:0018908|non-Hodgkin lymphoma","targets":["12367|NM_000546.6(TP53):c.974G>T (p.Gly325Val)|single nucleotide variant|Conflicting classifications of pathogenicity|TP53|criteria provided, conflicting classifications|17","13970|NM_004333.6(BRAF):c.1405G>C (p.Gly469Arg)|single nucleotide variant|Pathogenic/Likely pathogenic|BRAF|criteria provided, multiple submitters, no conflicts|7","13971|NM_004333.6(BRAF):c.1406G>C (p.Gly469Ala)|single nucleotide variant|Pathogenic|BRAF|criteria provided, single submitter|7","13972|NM_004333.6(BRAF):c.1781A>G (p.Asp594Gly)|single nucleotide variant|Pathogenic|BRAF|criteria provided, multiple submitters, no conflicts|7","31907|NM_004048.4(B2M):c.286G>A (p.Asp96Asn)|single nucleotide variant|Pathogenic|B2M|criteria provided, single submitter|15","5638|NM_012415.3(RAD54B):c.1778A>G (p.Asn593Ser)|single nucleotide variant|Benign|RAD54B|criteria provided, single submitter|8","6192|NM_003579.4(RAD54L):c.1331T>A (p.Val444Glu)|single nucleotide variant|Pathogenic|RAD54L|no assertion criteria provided|1","7765|NM_032977.4(CASP10):c.1241C>T (p.Ala414Val)|single nucleotide variant|Pathogenic|CASP10|no assertion criteria provided|2","7766|NM_032977.4(CASP10):c.769C>T (p.Gln257Ter)|single nucleotide variant|Pathogenic|CASP10|no assertion criteria provided|2","7767|NM_032977.4(CASP10):c.1042_1043insA (p.Gly348fs)|Insertion|Pathogenic|CASP10|no assertion criteria provided|2","801487|NM_003579.4(RAD54L):c.796G>C (p.Val266Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|RAD54L|criteria provided, conflicting classifications|1","801488|NM_003579.4(RAD54L):c.888C>T (p.Asp296=)|single nucleotide variant|Likely benign|RAD54L|criteria provided, multiple submitters, no conflicts|1","801489|NM_003579.4(RAD54L):c.1870-1G>A|single nucleotide variant|Uncertain significance|LRRC41|criteria provided, single submitter|1"]}]}