ClinVar Miner

List of variants in gene FMO3 reported as pathogenic for not provided

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Gene type:
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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_001002294.3(FMO3):c.913G>T (p.Glu305Ter) rs61753344 0.00035
NM_001002294.3(FMO3):c.1474C>T (p.Arg492Trp) rs72549334 0.00019
NM_001002294.3(FMO3):c.172G>A (p.Val58Ile) rs144935285 0.00016
NM_001002294.3(FMO3):c.1322T>C (p.Ile441Thr) rs535435928 0.00013
NM_001002294.3(FMO3):c.929C>T (p.Ser310Leu) rs572292275 0.00006
NM_001002294.3(FMO3):c.713G>A (p.Arg238Gln) rs748324481 0.00001
NC_000001.10:g.(?_171061800)_(171061951_?)del
NC_000001.10:g.(?_171061800)_(171073134_?)del
NC_000001.10:g.(?_171061800)_(171086582_?)del
NC_000001.10:g.(?_171076796)_(171086582_?)del
NC_000001.10:g.(?_171083127)_(171083522_?)del
NM_001002294.3(FMO3):c.1005C>A (p.Tyr335Ter)
NM_001002294.3(FMO3):c.102dup (p.Asn35fs)
NM_001002294.3(FMO3):c.1045G>T (p.Glu349Ter)
NM_001002294.3(FMO3):c.10A>T (p.Lys4Ter)
NM_001002294.3(FMO3):c.1118dup (p.Ser374fs)
NM_001002294.3(FMO3):c.1139_1140del (p.Pro380fs) rs775064534
NM_001002294.3(FMO3):c.1183+1del
NM_001002294.3(FMO3):c.1210del (p.Asp404fs)
NM_001002294.3(FMO3):c.1231G>T (p.Glu411Ter)
NM_001002294.3(FMO3):c.1237dup (p.Met413fs)
NM_001002294.3(FMO3):c.1257G>A (p.Trp419Ter)
NM_001002294.3(FMO3):c.1498C>T (p.Arg500Ter)
NM_001002294.3(FMO3):c.16del (p.Ala6fs)
NM_001002294.3(FMO3):c.170C>G (p.Ser57Ter)
NM_001002294.3(FMO3):c.174_175insA (p.Phe59fs)
NM_001002294.3(FMO3):c.1A>G (p.Met1Val)
NM_001002294.3(FMO3):c.209C>T (p.Pro70Leu)
NM_001002294.3(FMO3):c.22_29del (p.Ile8fs)
NM_001002294.3(FMO3):c.237del (p.Asn80fs)
NM_001002294.3(FMO3):c.674_690del (p.Trp225fs)
NM_001002294.3(FMO3):c.692G>A (p.Trp231Ter)
NM_001002294.3(FMO3):c.712C>T (p.Arg238Ter)
NM_001002294.3(FMO3):c.726_729del (p.Phe242fs)
NM_001002294.3(FMO3):c.762G>A (p.Trp254Ter)
NM_001002294.3(FMO3):c.768_769insAGATGACTG (p.Val257delinsArgTer)
NM_001002294.3(FMO3):c.775C>T (p.Gln259Ter)
NM_001002294.3(FMO3):c.778A>G (p.Met260Val)
NM_001002294.3(FMO3):c.839_842dup (p.Pro282fs)
NM_001002294.3(FMO3):c.859G>T (p.Glu287Ter) rs1057520649
NM_001002294.3(FMO3):c.993_994del (p.Tyr331_Ser332delinsTer) rs751356173

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