{"context":{"query":">>mondo>>clinvar","source_dataset":"mondo","target_dataset":"clinvar"},"stats":{"queried":1,"total":25,"mapped":1},"pagination":{"has_next":false},"schema":"id|name|type|germline_classification|gene_symbol|review_status|chromosome","mappings":[{"input":"MONDO:0005252","source":"MONDO:0005252|heart failure","targets":["1018253|NM_144573.4(NEXN):c.1302del (p.Ile435fs)|Deletion|Pathogenic/Likely pathogenic|NEXN|criteria provided, multiple submitters, no conflicts|1","13427|NM_000371.4(TTR):c.328C>A (p.His110Asn)|single nucleotide variant|Conflicting classifications of pathogenicity|TTR|criteria provided, conflicting classifications|18","178157|NM_001267550.2(TTN):c.102271C>T (p.Arg34091Trp)|single nucleotide variant|Conflicting classifications of pathogenicity|TTN-AS1|criteria provided, conflicting classifications|2","180947|NM_000256.3(MYBPC3):c.1720C>T (p.Arg574Trp)|single nucleotide variant|Uncertain significance|MYBPC3|criteria provided, multiple submitters, no conflicts|11","18156|NM_000021.4(PSEN1):c.998A>G (p.Asp333Gly)|single nucleotide variant|Conflicting classifications of pathogenicity|PSEN1|criteria provided, conflicting classifications|14","191549|NM_005751.5(AKAP9):c.139C>T (p.His47Tyr)|single nucleotide variant|Benign/Likely benign|AKAP9|criteria provided, multiple submitters, no conflicts|7","281070|NM_006790.3(MYOT):c.323A>C (p.Asn108Thr)|single nucleotide variant|Conflicting classifications of pathogenicity|MYOT|criteria provided, conflicting classifications|5","31819|NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile)|single nucleotide variant|Conflicting classifications of pathogenicity|MYPN|criteria provided, conflicting classifications|10","3769653|NM_000335.5(SCN5A):c.682A>G (p.Lys228Glu)|single nucleotide variant|Uncertain significance|SCN5A|criteria provided, single submitter|3","4070286|NM_001792.5(CDH2):c.1956G>C (p.Trp652Cys)|single nucleotide variant|Uncertain significance|CDH2|criteria provided, single submitter|18","44541|NM_002471.4(MYH6):c.622G>A (p.Asp208Asn)|single nucleotide variant|Benign/Likely benign|LOC114827851|criteria provided, multiple submitters, no conflicts|14","45711|NM_016203.4(PRKAG2):c.247C>T (p.Pro83Ser)|single nucleotide variant|Conflicting classifications of pathogenicity|PRKAG2|criteria provided, conflicting classifications|7","46595|NM_001267550.2(TTN):c.14984C>G (p.Pro4995Arg)|single nucleotide variant|Benign/Likely benign|TTN|criteria provided, multiple submitters, no conflicts|2","46614|NM_001267550.2(TTN):c.16303G>A (p.Val5435Met)|single nucleotide variant|Conflicting classifications of pathogenicity|TTN|criteria provided, conflicting classifications|2","470608|NM_001134363.3(RBM20):c.3169C>T (p.Arg1057Trp)|single nucleotide variant|Conflicting classifications of pathogenicity|RBM20|criteria provided, conflicting classifications|10","47160|NM_001267550.2(TTN):c.60232G>A (p.Val20078Met)|single nucleotide variant|Benign/Likely benign|TTN|criteria provided, multiple submitters, no conflicts|2","47184|NM_001267550.2(TTN):c.5479G>T (p.Ala1827Ser)|single nucleotide variant|Conflicting classifications of pathogenicity|TTN|criteria provided, conflicting classifications|2","47189|NM_001267550.2(TTN):c.63026G>A (p.Arg21009Gln)|single nucleotide variant|Benign/Likely benign|TTN|criteria provided, multiple submitters, no conflicts|2","47437|NM_001267550.2(TTN):c.84461C>T (p.Pro28154Leu)|single nucleotide variant|Benign/Likely benign|TTN|criteria provided, multiple submitters, no conflicts|2","497501|NM_004006.3(DMD):c.8083C>T (p.Pro2695Ser)|single nucleotide variant|Conflicting classifications of pathogenicity|DMD|criteria provided, conflicting classifications|X","519379|NM_005751.5(AKAP9):c.7208A>G (p.Glu2403Gly)|single nucleotide variant|Benign/Likely benign|AKAP9|criteria provided, multiple submitters, no conflicts|7","533010|NM_006790.3(MYOT):c.398C>T (p.Pro133Leu)|single nucleotide variant|Conflicting classifications of pathogenicity|MYOT|criteria provided, conflicting classifications|5","642106|NM_000257.4(MYH7):c.2641C>A (p.Leu881Met)|single nucleotide variant|Uncertain significance|LOC126861898|criteria provided, multiple submitters, no conflicts|14","691751|NM_001267550.2(TTN):c.33611A>C (p.Glu11204Ala)|single nucleotide variant|Conflicting classifications of pathogenicity|TTN|criteria provided, conflicting classifications|2","95440|NM_006790.3(MYOT):c.445G>C (p.Glu149Gln)|single nucleotide variant|Benign/Likely benign|MYOT|criteria provided, multiple submitters, no conflicts|5"]}]}