"Ambry Genetics"[submitter] AND "FMN1"[gene] - ClinVar

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Items: 69

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2314910	NM_001277313.2(FMN1):c.4246G>A (p.Val1416Met)	FMN1, LOC126862090 (V1193M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593242	NM_001277313.2(FMN1):c.4229G>A (p.Arg1410His)	FMN1, LOC126862090 (R1187H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309054	NM_001277313.2(FMN1):c.4121C>G (p.Ser1374Cys)	FMN1 (S1151C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271508	NM_001277313.2(FMN1):c.4102C>G (p.Arg1368Gly)	FMN1 (R1145G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232518	NM_001277313.2(FMN1):c.3998G>A (p.Arg1333Gln)	FMN1 (R1110Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2345047	NM_001277313.2(FMN1):c.3877A>G (p.Lys1293Glu)	FMN1 (K1070E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455914	NM_001277313.2(FMN1):c.3763T>G (p.Phe1255Val)	FMN1 (F1032V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2367321	NM_001277313.2(FMN1):c.3749C>T (p.Pro1250Leu)	FMN1 (P1250L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309688	NM_001277313.2(FMN1):c.3677A>C (p.Asp1226Ala)	FMN1 (D1226A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2462436	NM_001277313.2(FMN1):c.3592C>T (p.Arg1198Trp)	FMN1 (R1198W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2410002	NM_001277313.2(FMN1):c.3473A>G (p.His1158Arg)	FMN1 (H935R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2057159	NM_001277313.2(FMN1):c.3467C>G (p.Ser1156Cys)	FMN1 (S933C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2511627	NM_001277313.2(FMN1):c.3386A>T (p.His1129Leu)	FMN1 (H1129L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2363390	NM_001277313.2(FMN1):c.3343G>A (p.Glu1115Lys)	FMN1 (E1115K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2243024	NM_001277313.2(FMN1):c.3250G>A (p.Val1084Met)	FMN1 (V1084M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2257456	NM_001277313.2(FMN1):c.3090G>T (p.Lys1030Asn)	FMN1 (K1030N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2223020	NM_001277313.2(FMN1):c.3087G>T (p.Gln1029His)	FMN1 (Q1029H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2528381	NM_001277313.2(FMN1):c.3080C>T (p.Thr1027Ile)	FMN1 (T1027I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2392805	NM_001277313.2(FMN1):c.2935A>G (p.Ser979Gly)	FMN1 (S756G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2556014	NM_001277313.2(FMN1):c.2926A>G (p.Ile976Val)	FMN1 (I976V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593129	NM_001277313.2(FMN1):c.2846C>A (p.Pro949Gln)	FMN1 (P726Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2551618	NM_001277313.2(FMN1):c.2446T>C (p.Cys816Arg)	FMN1 (C593R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2398131	NM_001277313.2(FMN1):c.2430G>C (p.Glu810Asp)	FMN1 (E587D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2391888	NM_001277313.2(FMN1):c.2424C>G (p.Asp808Glu)	FMN1 (D585E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2252417	NM_001277313.2(FMN1):c.2371A>G (p.Thr791Ala)	FMN1 (T791A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2262341	NM_001277313.2(FMN1):c.2351G>A (p.Arg784Lys)	FMN1 (R784K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2614061	NM_001277313.2(FMN1):c.2349G>C (p.Glu783Asp)	FMN1 (E560D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2276153	NM_001277313.2(FMN1):c.2333G>A (p.Arg778Gln)	FMN1 (R778Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2305614	NM_001277313.2(FMN1):c.2292A>C (p.Glu764Asp)	FMN1 (E541D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2487459	NM_001277313.2(FMN1):c.2270T>C (p.Met757Thr)	FMN1 (M534T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2518649	NM_001277313.2(FMN1):c.2240G>A (p.Arg747Gln)	FMN1 (R524Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2539216	NM_001277313.2(FMN1):c.2224G>A (p.Ala742Thr)	FMN1 (A519T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2407081	NM_001277313.2(FMN1):c.2180T>C (p.Leu727Ser)	FMN1 (L504S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2248813	NM_001277313.2(FMN1):c.2170G>A (p.Ala724Thr)	FMN1 (A724T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2524645	NM_001277313.2(FMN1):c.2164T>C (p.Tyr722His)	FMN1 (Y499H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2454890	NM_001277313.2(FMN1):c.2110C>G (p.Pro704Ala)	FMN1 (P481A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2241815	NM_001277313.2(FMN1):c.2044-1456G>T	FMN1 (G452V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2589447	NM_001277313.2(FMN1):c.2044-1462C>T	FMN1 (A450V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2226650	NM_001277313.2(FMN1):c.2044-1529A>G	FMN1 (K428E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2507790	NM_001277313.2(FMN1):c.2044-1566G>C	FMN1 (K415N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2227079	NM_001277313.2(FMN1):c.2044-1579G>C	FMN1 (R411P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 593783	NM_001277313.2(FMN1):c.2044-1579G>A	FMN1 (R411Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2391393	NM_001277313.2(FMN1):c.2044-1580C>T	FMN1 (R411W)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2327570	NM_001277313.2(FMN1):c.2044-1583A>T	FMN1 (I410F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2608275	NM_001277313.2(FMN1):c.2044-1618C>T	FMN1 (P398L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2360504	NM_001277313.2(FMN1):c.2044-1666G>T	FMN1 (G382V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 500270	NM_001277313.2(FMN1):c.2044-1807C>T	FMN1 (P335L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2301545	NM_001277313.2(FMN1):c.2044-1846G>A	FMN1 (G322E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2289222	NM_001277313.2(FMN1):c.2044-1897T>C	FMN1 (L305S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 498508	NM_001277313.2(FMN1):c.2044-1910A>G	FMN1 (K301E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 499460	NM_001277313.2(FMN1):c.2044-1924C>T	FMN1 (T296M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2280587	NM_001277313.2(FMN1):c.2044-1936G>A	FMN1 (G292E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1505783	NM_001277313.2(FMN1):c.2044-2050G>A	FMN1 (G254D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2547654	NM_001277313.2(FMN1):c.2044-2083T>C	FMN1 (L243P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2068853	NM_001277313.2(FMN1):c.2044-2125G>A	FMN1 (R229H)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2371220	NM_001277313.2(FMN1):c.2044-2126C>T	FMN1 (R229C)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2200672	NM_001277313.2(FMN1):c.2044-2143G>A	FMN1 (G223D)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2264964	NM_001277313.2(FMN1):c.2044-2243A>G	FMN1 (N190D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2253887	NM_001277313.2(FMN1):c.2044-2257G>A	FMN1 (G185E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2206947	NM_001277313.2(FMN1):c.2044-2321A>G	FMN1 (N164D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2464217	NM_001277313.2(FMN1):c.2044-2329G>A	FMN1 (S161N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2613536	NM_001277313.2(FMN1):c.2044-2431T>C	FMN1 (L127S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2269013	NM_001277313.2(FMN1):c.2044-2474G>A	FMN1 (G113R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2283847	NM_001277313.2(FMN1):c.2044-2485G>A	FMN1 (R109K)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2275637	NM_001277313.2(FMN1):c.2044-2491G>A	FMN1 (S107N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1461875	NM_001277313.2(FMN1):c.2044-2537G>A	FMN1 (G92R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2360616	NM_001277313.2(FMN1):c.2044-2587G>C	FMN1 (S75T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2360001	NM_001277313.2(FMN1):c.2044-2626G>C	FMN1 (S62T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2052479	NM_001277313.2(FMN1):c.2044-2659A>G	FMN1 (E51G)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance

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Items: 69