ZNF154[gene] and "single gene"[properties] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2238642	NM_001085384.3(ZNF154):c.1262C>T (p.Ser421Phe)	ZNF154 (S421F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261213	NM_001085384.3(ZNF154):c.1232A>G (p.Lys411Arg)	ZNF154 (K411R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2225749	NM_001085384.3(ZNF154):c.1161C>G (p.Cys387Trp)	ZNF154 (C387W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194095	NM_001085384.3(ZNF154):c.1055C>A (p.Thr352Asn)	ZNF154 (T352N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345310	NM_001085384.3(ZNF154):c.1043G>A (p.Arg348Gln)	ZNF154 (R348Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353347	NM_001085384.3(ZNF154):c.1042C>T (p.Arg348Trp)	ZNF154 (R348W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334997	NM_001085384.3(ZNF154):c.986A>G (p.Tyr329Cys)	ZNF154 (Y329C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194104	NM_001085384.3(ZNF154):c.979A>G (p.Arg327Gly)	ZNF154 (R327G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334994	NM_001085384.3(ZNF154):c.951T>G (p.Ile317Met)	ZNF154 (I317M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334993	NM_001085384.3(ZNF154):c.949A>T (p.Ile317Phe)	ZNF154 (I317F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334996	NM_001085384.3(ZNF154):c.907T>G (p.Cys303Gly)	ZNF154 (C303G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273700	NM_001085384.3(ZNF154):c.904G>A (p.Glu302Lys)	ZNF154 (E302K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269823	NM_001085384.3(ZNF154):c.833G>A (p.Cys278Tyr)	ZNF154 (C278Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492980	NM_001085384.3(ZNF154):c.764G>A (p.Ser255Asn)	ZNF154 (S255N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237987	NM_001085384.3(ZNF154):c.745G>C (p.Glu249Gln)	ZNF154 (E249Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215645	NM_001085384.3(ZNF154):c.742A>G (p.Ser248Gly)	ZNF154 (S248G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194103	NM_001085384.3(ZNF154):c.713T>G (p.Val238Gly)	ZNF154 (V238G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361469	NM_001085384.3(ZNF154):c.707G>A (p.Arg236Gln)	ZNF154 (R236Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194101	NM_001085384.3(ZNF154):c.572G>A (p.Cys191Tyr)	ZNF154 (C191Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369531	NM_001085384.3(ZNF154):c.415A>G (p.Thr139Ala)	ZNF154 (T139A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194099	NM_001085384.3(ZNF154):c.382A>G (p.Arg128Gly)	ZNF154 (R128G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373801	NM_001085384.3(ZNF154):c.364G>A (p.Gly122Ser)	ZNF154 (G122S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2608387	NM_001085384.3(ZNF154):c.305T>C (p.Leu102Ser)	ZNF154 (L102S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334995	NM_001085384.3(ZNF154):c.299C>A (p.Ala100Asp)	ZNF154 (A100D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194098	NM_001085384.3(ZNF154):c.239G>A (p.Cys80Tyr)	ZNF154 (C80Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194097	NM_001085384.3(ZNF154):c.220G>C (p.Ala74Pro)	ZNF154 (A74P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194096	NM_001085384.3(ZNF154):c.200T>C (p.Phe67Ser)	ZNF154 (F67S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610294	NM_001085384.3(ZNF154):c.163G>A (p.Val55Ile)	ZNF154 (V55I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389016	NM_001085384.3(ZNF154):c.142G>A (p.Ala48Thr)	ZNF154 (A48T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274484	NM_001085384.3(ZNF154):c.88C>G (p.Leu30Val)	ZNF154 (L30V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194102	NM_001085384.3(ZNF154):c.66C>G (p.His22Gln)	ZNF154 (H22Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194100	NM_001085384.3(ZNF154):c.38C>T (p.Thr13Ile)	ZNF154 (T13I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 32