"Ambry Genetics"[submitter] AND "ZNF669"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2394031	NM_001142572.2(ZNF669):c.1123G>A (p.Val375Met)	ZNF669 (V461M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232438	NM_001142572.2(ZNF669):c.1115G>T (p.Gly372Val)	ZNF669 (G372V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2515827	NM_001142572.2(ZNF669):c.1109T>C (p.Leu370Ser)	ZNF669 (L370S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2260582	NM_001142572.2(ZNF669):c.907C>T (p.Pro303Ser)	ZNF669 (P303S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309954	NM_001142572.2(ZNF669):c.860G>A (p.Arg287His)	ZNF669 (R287H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2282014	NM_001142572.2(ZNF669):c.806T>G (p.Ile269Ser)	ZNF669 (I269S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2390397	NM_001142572.2(ZNF669):c.791G>A (p.Arg264His)	ZNF669 (R350H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2308183	NM_001142572.2(ZNF669):c.698G>A (p.Cys233Tyr)	ZNF669 (C233Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2206134	NM_001142572.2(ZNF669):c.613G>A (p.Gly205Ser)	ZNF669 (G205S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309090	NM_001142572.2(ZNF669):c.571C>G (p.Pro191Ala)	ZNF669 (P191A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2511792	NM_001142572.2(ZNF669):c.471G>A (p.Met157Ile)	ZNF669 (M157I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2477919	NM_001142572.2(ZNF669):c.383A>G (p.Tyr128Cys)	ZNF669 (Y214C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2539539	NM_001142572.2(ZNF669):c.239A>G (p.Tyr80Cys)	ZNF669 (Y80C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2270691	NM_001142572.2(ZNF669):c.198T>G (p.His66Gln)	ZNF669 (H152Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2396164	NM_001142572.2(ZNF669):c.197A>G (p.His66Arg)	ZNF669 (H152R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2210479	NM_001142572.2(ZNF669):c.188T>G (p.Ile63Arg)	ZNF669 (I149R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351524	NM_001142572.2(ZNF669):c.109T>G (p.Cys37Gly)	ZNF669 (C123G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2280604	NM_001142572.2(ZNF669):c.86A>G (p.Tyr29Cys)	ZNF669 (Y29C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2335803	NM_001142572.2(ZNF669):c.28G>A (p.Ala10Thr)	ZNF669 (A10T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2212110	NM_001142572.2(ZNF669):c.3+248C>A	ZNF669 (S84Y)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2274425	NM_001142572.2(ZNF669):c.3+190G>C	ZNF669 (V65L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2304177	NM_001142572.2(ZNF669):c.3+10C>G	ZNF669 (L5V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 22