"Ambry Genetics"[submitter] AND "ZNF91"[gene] - ClinVar

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2457323	NM_003430.4(ZNF91):c.3509C>T (p.Ala1170Val)	ZNF91 (A1138V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2344854	NM_003430.4(ZNF91):c.3496T>A (p.Trp1166Arg)	ZNF91 (W1134R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2225424	NM_003430.4(ZNF91):c.3494T>G (p.Leu1165Arg)	ZNF91 (L1133R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2320697	NM_003430.4(ZNF91):c.3437C>T (p.Ser1146Phe)	ZNF91 (S1114F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2470474	NM_003430.4(ZNF91):c.3424G>T (p.Ala1142Ser)	ZNF91 (A1110S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2248987	NM_003430.4(ZNF91):c.3373A>G (p.Lys1125Glu)	ZNF91 (K1125E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2383721	NM_003430.4(ZNF91):c.3347A>G (p.Lys1116Arg)	ZNF91 (K1084R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2306443	NM_003430.4(ZNF91):c.3281C>G (p.Thr1094Ser)	ZNF91 (T1062S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2519726	NM_003430.4(ZNF91):c.3149A>G (p.Tyr1050Cys)	ZNF91 (Y1050C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2253958	NM_003430.4(ZNF91):c.3070T>C (p.Cys1024Arg)	ZNF91 (C1024R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2221727	NM_003430.4(ZNF91):c.2825A>C (p.Glu942Ala)	ZNF91 (E910A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2318798	NM_003430.4(ZNF91):c.2735G>A (p.Cys912Tyr)	ZNF91 (C912Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2318364	NM_003430.4(ZNF91):c.2731A>G (p.Lys911Glu)	ZNF91 (K911E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2308786	NM_003430.4(ZNF91):c.2641C>T (p.Pro881Ser)	ZNF91 (P881S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2204760	NM_003430.4(ZNF91):c.2609C>G (p.Thr870Arg)	ZNF91 (T870R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2394759	NM_003430.4(ZNF91):c.2575T>C (p.Cys859Arg)	ZNF91 (C859R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2541908	NM_003430.4(ZNF91):c.2561A>T (p.Tyr854Phe)	ZNF91 (Y854F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2522565	NM_003430.4(ZNF91):c.2556A>C (p.Lys852Asn)	ZNF91 (K820N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2538619	NM_003430.4(ZNF91):c.2351C>T (p.Thr784Ile)	ZNF91 (T752I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2392485	NM_003430.4(ZNF91):c.2143A>G (p.Lys715Glu)	ZNF91 (K683E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2382763	NM_003430.4(ZNF91):c.2114A>G (p.Lys705Arg)	ZNF91 (K673R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2410135	NM_003430.4(ZNF91):c.2090G>A (p.Arg697Gln)	ZNF91 (R697Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2354087	NM_003430.4(ZNF91):c.2032A>G (p.Ile678Val)	ZNF91 (I678V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2599339	NM_003430.4(ZNF91):c.1936G>A (p.Ala646Thr)	ZNF91 (A646T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2207522	NM_003430.4(ZNF91):c.1922A>G (p.His641Arg)	ZNF91 (H609R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2266541	NM_003430.4(ZNF91):c.1921C>T (p.His641Tyr)	ZNF91 (H609Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2402993	NM_003430.4(ZNF91):c.1782A>G (p.Ile594Met)	ZNF91 (I562M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2570511	NM_003430.4(ZNF91):c.1750A>C (p.Asn584His)	ZNF91 (N552H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2242397	NM_003430.4(ZNF91):c.1652G>T (p.Cys551Phe)	ZNF91 (C551F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2304783	NM_003430.4(ZNF91):c.1574A>G (p.Lys525Arg)	ZNF91 (K525R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2208797	NM_003430.4(ZNF91):c.1535A>G (p.His512Arg)	ZNF91 (H512R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2526804	NM_003430.4(ZNF91):c.1286C>T (p.Thr429Ile)	ZNF91 (T429I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2473227	NM_003430.4(ZNF91):c.1091C>T (p.Thr364Ile)	ZNF91 (T364I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2495500	NM_003430.4(ZNF91):c.1085C>T (p.Ser362Phe)	ZNF91 (S330F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2465086	NM_003430.4(ZNF91):c.1053A>T (p.Lys351Asn)	ZNF91 (K351N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2457812	NM_003430.4(ZNF91):c.1022A>C (p.Lys341Thr)	ZNF91 (K341T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2214012	NM_003430.4(ZNF91):c.718T>C (p.Cys240Arg)	ZNF91 (C240R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2603054	NM_003430.4(ZNF91):c.697A>C (p.Thr233Pro)	ZNF91 (T233P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2366109	NM_003430.4(ZNF91):c.670A>G (p.Thr224Ala)	ZNF91 (T224A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2386765	NM_003430.4(ZNF91):c.607G>A (p.Val203Ile)	ZNF91 (V171I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2216280	NM_003430.4(ZNF91):c.581G>A (p.Arg194His)	ZNF91 (R162H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2319843	NM_003430.4(ZNF91):c.517A>G (p.Thr173Ala)	ZNF91 (T141A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2558110	NM_003430.4(ZNF91):c.427A>T (p.Asn143Tyr)	ZNF91 (N111Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493804	NM_003430.4(ZNF91):c.377G>T (p.Cys126Phe)	ZNF91 (C126F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2381569	NM_003430.4(ZNF91):c.377G>A (p.Cys126Tyr)	ZNF91 (C94Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2535437	NM_003430.4(ZNF91):c.238G>A (p.Val80Met)	ZNF91 (V80M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 46