"Ambry Genetics"[submitter] AND "ZNF841"[gene] - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2516601	NM_001136499.2(ZNF841):c.2756C>T (p.Thr919Ile)	LOC126862922, ZNF841 (T803I +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2244091	NM_001136499.2(ZNF841):c.2698G>A (p.Ala900Thr)	LOC126862922, ZNF841 (A901T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2409294	NM_001136499.2(ZNF841):c.2665C>T (p.Arg889Cys)	LOC126862922, ZNF841 (R773C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2297880	NM_001136499.2(ZNF841):c.2578C>T (p.Arg860Trp)	LOC126862922, ZNF841 (R744W +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2204091	NM_001136499.2(ZNF841):c.2450G>T (p.Gly817Val)	LOC126862922, ZNF841 (G817V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2516616	NM_001136499.2(ZNF841):c.2434C>G (p.Gln812Glu)	LOC126862922, ZNF841 (Q696E +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2295264	NM_001136499.2(ZNF841):c.2419A>G (p.Ile807Val)	LOC126862922, ZNF841 (I691V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2351639	NM_001136499.2(ZNF841):c.2414G>A (p.Arg805His)	LOC126862922, ZNF841 (R806H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2400179	NM_001136499.2(ZNF841):c.2413C>T (p.Arg805Cys)	LOC126862922, ZNF841 (R805C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2268222	NM_001136499.2(ZNF841):c.2338C>T (p.Leu780Phe)	LOC126862922, ZNF841 (L781F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2390456	NM_001136499.2(ZNF841):c.1861G>A (p.Gly621Arg)	LOC126862922, ZNF841 (G622R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2470437	NM_001136499.2(ZNF841):c.1850G>A (p.Arg617Gln)	ZNF841, LOC126862922 (R617Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2204058	NM_001136499.2(ZNF841):c.1820T>C (p.Ile607Thr)	ZNF841, LOC126862922 (I491T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2523503	NM_001136499.2(ZNF841):c.1720T>C (p.Cys574Arg)	LOC126862922, ZNF841 (C574R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2215042	NM_001136499.2(ZNF841):c.1561G>A (p.Ala521Thr)	ZNF841 (A522T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2561101	NM_001136499.2(ZNF841):c.1528G>A (p.Glu510Lys)	ZNF841 (E511K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2610124	NM_001136499.2(ZNF841):c.1521T>G (p.His507Gln)	ZNF841 (H507Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2304942	NM_001136499.2(ZNF841):c.1517T>C (p.Val506Ala)	ZNF841 (V506A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2510616	NM_001136499.2(ZNF841):c.1427G>A (p.Arg476Gln)	ZNF841 (R476Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2460816	NM_001136499.2(ZNF841):c.1426C>T (p.Arg476Trp)	ZNF841 (R477W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2552294	NM_001136499.2(ZNF841):c.1394T>C (p.Val465Ala)	ZNF841 (V466A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2224565	NM_001136499.2(ZNF841):c.1339C>T (p.His447Tyr)	ZNF841 (H331Y +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378886	NM_001136499.2(ZNF841):c.1210A>G (p.Asn404Asp)	ZNF841 (N288D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2242124	NM_001136499.2(ZNF841):c.1168A>G (p.Thr390Ala)	ZNF841 (T391A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2283636	NM_001136499.2(ZNF841):c.1021G>A (p.Gly341Arg)	ZNF841 (G341R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2292587	NM_001136499.2(ZNF841):c.896A>G (p.His299Arg)	ZNF841 (H299R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488422	NM_001136499.2(ZNF841):c.851C>T (p.Thr284Ile)	ZNF841 (T168I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2349560	NM_001136499.2(ZNF841):c.827T>C (p.Leu276Pro)	ZNF841 (L276P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2241730	NM_001136499.2(ZNF841):c.796T>A (p.Cys266Ser)	ZNF841 (C266S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2407742	NM_001136499.2(ZNF841):c.764A>G (p.His255Arg)	ZNF841 (H256R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2340319	NM_001136499.2(ZNF841):c.539T>C (p.Met180Thr)	ZNF841 (M181T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377566	NM_001136499.2(ZNF841):c.523G>A (p.Val175Ile)	ZNF841 (V59I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615221	NM_001136499.2(ZNF841):c.512G>C (p.Ser171Thr)	ZNF841 (S172T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2612598	NM_001136499.2(ZNF841):c.393C>G (p.Phe131Leu)	ZNF841 (F132L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2381622	NM_001136499.2(ZNF841):c.368G>A (p.Ser123Asn)	ZNF841 (S124N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315318	NM_001136499.2(ZNF841):c.133G>A (p.Gly45Ser)	ZNF841 (G45S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2325126	NM_001136499.2(ZNF841):c.7C>G (p.Leu3Val)	ZNF841 (L3V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 37