FMO3[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 293685	NM_001002294.3(FMO3):c.-25G>A	FMO3	Single nucleotide variant (5 prime UTR variant)	Trimethylaminuria	GUncertain significance
Select item 2506224	NM_001002294.3(FMO3):c.-6-1G>C	FMO3	Single nucleotide variant (splice acceptor variant)	not specified	GUncertain significance
Select item 2898902	NM_001002294.3(FMO3):c.1A>G (p.Met1Val)	FMO3 (M1V)	Single nucleotide variant (missense variant +2 more)	not provided	GPathogenic
Select item 3013899	NM_001002294.3(FMO3):c.10A>T (p.Lys4Ter)	FMO3 (K4*)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 2696531	NM_001002294.3(FMO3):c.16del (p.Ala6fs)	FMO3 (A6fs)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 2766791	NM_001002294.3(FMO3):c.22_29del (p.Ile8fs)	FMO3 (I8fs)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 2709014	NM_001002294.3(FMO3):c.21C>T (p.Ile7=)	FMO3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2481182	NM_001002294.3(FMO3):c.29C>T (p.Ala10Val)	FMO3 (A10V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3279353	NM_001002294.3(FMO3):c.41G>A (p.Gly14Asp)	FMO3 (G14D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2848765	NM_001002294.3(FMO3):c.42C>T (p.Gly14=)	FMO3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3029305	NM_001002294.3(FMO3):c.50C>T (p.Ser17Phe)	FMO3 (S17F)	Single nucleotide variant (missense variant +1 more)	FMO3-related disorder	GUncertain significance
Select item 2849607	NM_001002294.3(FMO3):c.81G>A (p.Glu27=)	FMO3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 16316	NM_001002294.3(FMO3):c.94G>A (p.Glu32Lys)	FMO3 (E32K)	Single nucleotide variant (missense variant +1 more)	Trimethylaminuria	GPathogenic
Select item 3095895	NM_001002294.3(FMO3):c.98A>G (p.Lys33Arg)	FMO3 (K33R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2857220	NM_001002294.3(FMO3):c.102dup (p.Asn35fs)	FMO3 (N35fs)	Duplication (frameshift variant +1 more)	not provided	GPathogenic
Select item 3279352	NM_001002294.3(FMO3):c.118C>G (p.Leu40Val)	FMO3 (L40V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 260067	NM_001002294.3(FMO3):c.132+1G>T	FMO3	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2820249	NM_001002294.3(FMO3):c.132+9C>G	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2703259	NM_001002294.3(FMO3):c.132+11T>C	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2840902	NM_001002294.3(FMO3):c.132+12G>A	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 874915	NM_001002294.3(FMO3):c.132+13T>C	FMO3	Single nucleotide variant (intron variant)	Trimethylaminuria	GUncertain significance
Select item 2744392	NM_001002294.3(FMO3):c.132+15G>C	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3036104	NM_001002294.3(FMO3):c.133-2658A>T	FMO3	Single nucleotide variant (5 prime UTR variant +1 more)	FMO3-related disorder	GLikely benign
Select item 2822685	NM_001002294.3(FMO3):c.133-2A>G	FMO3	Single nucleotide variant (splice acceptor variant +1 more)	not provided	GLikely pathogenic
Select item 2662180	NM_001002294.3(FMO3):c.151A>G (p.Arg51Gly)	FMO3 (R31G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic
Select item 16307	NM_001002294.3(FMO3):c.154G>A (p.Ala52Thr)	FMO3 (A52T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2744460	NM_001002294.3(FMO3):c.170C>G (p.Ser57Ter)	FMO3 (S37* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided	GPathogenic
Select item 225365	NM_001002294.3(FMO3):c.172G>A (p.Val58Ile)	FMO3 (V58I +1 more)	Single nucleotide variant (missense variant +1 more)	Trimethylaminuria +2 more	GConflicting classifications of pathogenicity
Select item 2840209	NM_001002294.3(FMO3):c.174_175insA (p.Phe59fs)	FMO3 (F59fs +1 more)	Insertion (frameshift variant +1 more)	not provided	GPathogenic
Select item 16313	NM_001002294.3(FMO3):c.182A>G (p.Asn61Ser)	FMO3 (N61S +1 more)	Single nucleotide variant (missense variant +1 more)	Trimethylaminuria	GLikely pathogenic
Select item 16317	NM_001002294.3(FMO3):c.192del (p.Glu65fs)	FMO3 (E45fs +1 more)	Deletion (frameshift variant +1 more)	Trimethylaminuria	GPathogenic
Select item 16306	NM_001002294.3(FMO3):c.198G>T (p.Met66Ile)	FMO3 (M66I +1 more)	Single nucleotide variant (missense variant +1 more)	Trimethylaminuria	GLikely pathogenic
Select item 2734029	NM_001002294.3(FMO3):c.209C>T (p.Pro70Leu)	FMO3 (P70L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GPathogenic
Select item 293686	NM_001002294.3(FMO3):c.225C>T (p.Pro75=)	FMO3	Single nucleotide variant (synonymous variant +1 more)	Trimethylaminuria +1 more	GConflicting classifications of pathogenicity
Select item 2828328	NM_001002294.3(FMO3):c.237del (p.Asn80fs)	FMO3 (N80fs +1 more)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 293687	NM_001002294.3(FMO3):c.245T>C (p.Met82Thr)	FMO3 (M82T +1 more)	Single nucleotide variant (missense variant +1 more)	Trimethylaminuria	GUncertain significance
Select item 293688	NM_001002294.3(FMO3):c.260T>A (p.Ile87Asn)	FMO3 (I87N +1 more)	Single nucleotide variant (missense variant +1 more)	Trimethylaminuria	GUncertain significance
Select item 3095892	NM_001002294.3(FMO3):c.305A>G (p.Lys102Arg)	FMO3 (K102R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2837854	NM_001002294.3(FMO3):c.321+1G>T	FMO3	Single nucleotide variant (splice donor variant +1 more)	not provided	GLikely pathogenic
Select item 260070	NM_001002294.3(FMO3):c.321+31C>A	FMO3	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 260071	NM_001002294.3(FMO3):c.321+44_321+46del	FMO3	Microsatellite (intron variant)	not specified	GLikely benign
Select item 2890945	NM_001002294.3(FMO3):c.322-8T>C	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2703563	NM_001002294.3(FMO3):c.322-6T>C	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 875848	NM_001002294.3(FMO3):c.329T>C (p.Val110Ala)	FMO3 (V110A +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 875849	NM_001002294.3(FMO3):c.341A>G (p.Asn114Ser)	FMO3 (N114S +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +2 more	GConflicting classifications of pathogenicity
Select item 293690	NM_001002294.3(FMO3):c.628-6T>C	FMO3	Single nucleotide variant (intron variant)	Trimethylaminuria +1 more	GConflicting classifications of pathogenicity
Select item 2770970	NM_001002294.3(FMO3):c.628-1G>A	FMO3	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 876847	NM_001002294.3(FMO3):c.660G>A (p.Val220=)	FMO3	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1321151	NM_001002294.3(FMO3):c.667C>T (p.Arg223Trp)	FMO3 (R160W +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GLikely pathogenic
Select item 2734030	NM_001002294.3(FMO3):c.668G>A (p.Arg223Gln)	FMO3 (R160Q +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2700823	NM_001002294.3(FMO3):c.674_690del (p.Trp225fs)	FMO3 (W162fs +2 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 2556156	NM_001002294.3(FMO3):c.673T>G (p.Trp225Gly)	FMO3 (W205G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 876848	NM_001002294.3(FMO3):c.684T>C (p.Gly228=)	FMO3	Single nucleotide variant (synonymous variant)	Trimethylaminuria	GUncertain significance
Select item 2852024	NM_001002294.3(FMO3):c.692G>A (p.Trp231Ter)	FMO3 (W211* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2859217	NM_001002294.3(FMO3):c.700C>T (p.Leu234=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 293691	NM_001002294.3(FMO3):c.706G>A (p.Val236Ile)	FMO3 (V236I +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2725075	NM_001002294.3(FMO3):c.712C>A (p.Arg238=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2719491	NM_001002294.3(FMO3):c.712C>T (p.Arg238Ter)	FMO3 (R175* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 874042	NM_001002294.3(FMO3):c.713G>A (p.Arg238Gln)	FMO3 (R218Q +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2833474	NM_001002294.3(FMO3):c.726_729del (p.Phe242fs)	FMO3 (F222fs +2 more)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 874043	NM_001002294.3(FMO3):c.729C>G (p.Leu243=)	FMO3	Single nucleotide variant (synonymous variant)	Trimethylaminuria	GUncertain significance
Select item 874044	NM_001002294.3(FMO3):c.743C>T (p.Pro248Leu)	FMO3 (P185L +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 2825666	NM_001002294.3(FMO3):c.744G>A (p.Pro248=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2830456	NM_001002294.3(FMO3):c.768C>T (p.Tyr256=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2708285	NM_001002294.3(FMO3):c.768_769insAGATGACTG (p.Val257delinsArgTer)	FMO3	Insertion (nonsense)	not provided	GPathogenic
Select item 16305	NM_001002294.3(FMO3):c.769G>A (p.Val257Met)	FMO3 (V257M +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 2734480	NM_001002294.3(FMO3):c.775C>T (p.Gln259Ter)	FMO3 (Q196* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2734031	NM_001002294.3(FMO3):c.778A>G (p.Met260Val)	FMO3 (M197V +2 more)	Single nucleotide variant (missense variant)	not provided	GPathogenic
Select item 2920389	NM_001002294.3(FMO3):c.807T>C (p.Tyr269=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2853237	NM_001002294.3(FMO3):c.825_827+16del	FMO3	Deletion (splice donor variant)	not provided	GLikely pathogenic
Select item 2815399	NM_001002294.3(FMO3):c.827+9G>A	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2850691	NM_001002294.3(FMO3):c.827+17C>T	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2823942	NM_001002294.3(FMO3):c.827+18G>A	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2821206	NM_001002294.3(FMO3):c.827+19T>C	FMO3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2707273	NM_001002294.3(FMO3):c.828-13G>C	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2822922	NM_001002294.3(FMO3):c.828-12T>C	FMO3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3064195	NM_001002294.3(FMO3):c.828-2A>G	FMO3	Single nucleotide variant (splice acceptor variant)	Trimethylaminuria	GLikely pathogenic
Select item 260077	NM_001002294.3(FMO3):c.830T>C (p.Val277Ala)	FMO3 (V277A +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign/Likely benign
Select item 2863131	NM_001002294.3(FMO3):c.839_842dup (p.Pro282fs)	FMO3 (P282fs +2 more)	Duplication (frameshift variant)	not provided	GPathogenic
Select item 260078	NM_001002294.3(FMO3):c.855C>T (p.Asn285=)	FMO3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 379574	NM_001002294.3(FMO3):c.859G>T (p.Glu287Ter)	FMO3 (E287* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2237393	NM_001002294.3(FMO3):c.874A>G (p.Ile292Val)	FMO3 (I272V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3348369	NM_001002294.3(FMO3):c.877_878del (p.Leu293fs)	FMO3 (L230fs +2 more)	Deletion (frameshift variant)	FMO3-related disorder	GLikely pathogenic
Select item 2816085	NM_001002294.3(FMO3):c.885C>T (p.Gly295=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 293692	NM_001002294.3(FMO3):c.889G>T (p.Val297Leu)	FMO3 (V297L +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria	GUncertain significance
Select item 2842448	NM_001002294.3(FMO3):c.894C>T (p.Ser298=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2779287	NM_001002294.3(FMO3):c.900G>A (p.Lys300=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 721720	NM_001002294.3(FMO3):c.906C>T (p.Asn302=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2698966	NM_001002294.3(FMO3):c.912G>A (p.Lys304=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 16304	NM_001002294.3(FMO3):c.913G>T (p.Glu305Ter)	FMO3 (E305* +2 more)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic
Select item 2577331	NM_001002294.3(FMO3):c.919A>C (p.Thr307Pro)	FMO3 (T244P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 38395	NM_001002294.3(FMO3):c.923A>G (p.Glu308Gly)	FMO3 (E308G +2 more)	Single nucleotide variant (missense variant)	Trimethylaminuria +2 more	GBenign/Likely benign
Select item 2495582	NM_001002294.3(FMO3):c.926C>T (p.Thr309Ile)	FMO3 (T289I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 631576	NM_001002294.3(FMO3):c.929C>T (p.Ser310Leu)	FMO3 (S310L +2 more)	Single nucleotide variant (missense variant)	See cases +2 more	GLikely pathogenic
Select item 2959408	NM_001002294.3(FMO3):c.930G>A (p.Ser310=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 16312	NM_001002294.3(FMO3):c.940G>T (p.Glu314Ter)	FMO3 (E314* +2 more)	Single nucleotide variant (nonsense)	Trimethylaminuria	GPathogenic
Select item 2833616	NM_001002294.3(FMO3):c.951C>T (p.Thr317=)	FMO3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 260079	NM_001002294.3(FMO3):c.969C>T (p.Asp323=)	FMO3	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 2383527	NM_001002294.3(FMO3):c.971G>C (p.Cys324Ser)	FMO3 (C261S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 293693	NM_001002294.3(FMO3):c.979T>G (p.Phe327Val)	FMO3 (F327V +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

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