"Ambry Genetics"[submitter] AND "ZNF181"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2551368	NM_001029997.4(ZNF181):c.36C>A (p.Asp12Glu)	ZNF181 (D12E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360756	NM_001029997.4(ZNF181):c.131C>G (p.Ala44Gly)	ZNF181 (A44G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400333	NM_001029997.4(ZNF181):c.305T>A (p.Val102Glu)	ZNF181 (V102E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194229	NM_001029997.4(ZNF181):c.322G>T (p.Val108Leu)	ZNF181 (V108L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335062	NM_001029997.4(ZNF181):c.385G>A (p.Gly129Arg)	ZNF181 (G128R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589299	NM_001029997.4(ZNF181):c.407A>C (p.Asp136Ala)	ZNF181 (D136A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287424	NM_001029997.4(ZNF181):c.414C>G (p.Phe138Leu)	ZNF181 (F138L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194230	NM_001029997.4(ZNF181):c.437G>C (p.Arg146Thr)	ZNF181 (R145T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512697	NM_001029997.4(ZNF181):c.527T>A (p.Ile176Asn)	ZNF181 (I176N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284360	NM_001029997.4(ZNF181):c.535G>A (p.Glu179Lys)	ZNF181 (E179K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194232	NM_001029997.4(ZNF181):c.604A>G (p.Lys202Glu)	ZNF181 (K202E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530419	NM_001029997.4(ZNF181):c.724T>C (p.Cys242Arg)	ZNF181 (C242R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335061	NM_001029997.4(ZNF181):c.733G>A (p.Ala245Thr)	ZNF181 (A245T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221249	NM_001029997.4(ZNF181):c.734C>T (p.Ala245Val)	ZNF181 (A244V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346524	NM_001029997.4(ZNF181):c.760C>T (p.Arg254Cys)	ZNF181 (R254C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306967	NM_001029997.4(ZNF181):c.761G>T (p.Arg254Leu)	ZNF181 (R253L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615716	NM_001029997.4(ZNF181):c.770G>T (p.Arg257Ile)	ZNF181 (R256I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568598	NM_001029997.4(ZNF181):c.803G>A (p.Arg268His)	ZNF181 (R267H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2389537	NM_001029997.4(ZNF181):c.833C>T (p.Ser278Leu)	ZNF181 (S277L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364042	NM_001029997.4(ZNF181):c.993T>G (p.Ser331Arg)	ZNF181 (S330R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486213	NM_001029997.4(ZNF181):c.1046A>G (p.Tyr349Cys)	ZNF181 (Y348C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263872	NM_001029997.4(ZNF181):c.1109T>G (p.Ile370Ser)	ZNF181 (I370S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242315	NM_001029997.4(ZNF181):c.1181G>C (p.Arg394Pro)	ZNF181 (R394P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360665	NM_001029997.4(ZNF181):c.1199C>T (p.Thr400Ile)	ZNF181 (T399I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314644	NM_001029997.4(ZNF181):c.1293A>T (p.Lys431Asn)	ZNF181 (K431N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594069	NM_001029997.4(ZNF181):c.1384G>A (p.Glu462Lys)	ZNF181 (E462K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3335060	NM_001029997.4(ZNF181):c.1394T>C (p.Ile465Thr)	ZNF181 (I465T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461578	NM_001029997.4(ZNF181):c.1424C>T (p.Ser475Phe)	ZNF181 (S474F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549838	NM_001029997.4(ZNF181):c.1524G>C (p.Gln508His)	ZNF181 (Q508H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455975	NM_001029997.4(ZNF181):c.1534A>G (p.Thr512Ala)	ZNF181 (T512A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390828	NM_001029997.4(ZNF181):c.1562A>G (p.Glu521Gly)	ZNF181 (E521G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380701	NM_001029997.4(ZNF181):c.1606C>G (p.Gln536Glu)	ZNF181 (Q535E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400332	NM_001029997.4(ZNF181):c.1667A>C (p.Tyr556Ser)	ZNF181 (Y556S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621032	NM_001029997.4(ZNF181):c.1682C>T (p.Thr561Ile)	ZNF181 (T560I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3194228	NM_001029997.4(ZNF181):c.1687G>A (p.Glu563Lys)	ZNF181 (E562K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 35