"Ambry Genetics"[submitter] AND "ZNF35"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2294215	NM_003420.4(ZNF35):c.121G>A (p.Glu41Lys)	ZKSCAN7-AS1, ZNF35 (E41K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2330727	NM_003420.4(ZNF35):c.133G>A (p.Val45Ile)	ZKSCAN7-AS1, ZNF35 (V45I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455665	NM_003420.4(ZNF35):c.308T>C (p.Leu103Pro)	ZKSCAN7-AS1, ZNF35 (L103P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2593455	NM_003420.4(ZNF35):c.456A>C (p.Leu152Phe)	ZKSCAN7-AS1, ZNF35 (L152F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2462007	NM_003420.4(ZNF35):c.479A>T (p.Asn160Ile)	ZKSCAN7-AS1, ZNF35 (N160I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247473	NM_003420.4(ZNF35):c.565A>G (p.Lys189Glu)	ZKSCAN7-AS1, ZNF35 (K189E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2342934	NM_003420.4(ZNF35):c.578A>C (p.Asn193Thr)	ZKSCAN7-AS1, ZNF35 (N193T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2531257	NM_003420.4(ZNF35):c.605A>C (p.Lys202Thr)	ZKSCAN7-AS1, ZNF35 (K202T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2233179	NM_003420.4(ZNF35):c.608A>G (p.Tyr203Cys)	ZKSCAN7-AS1, ZNF35 (Y203C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493058	NM_003420.4(ZNF35):c.676G>A (p.Val226Met)	ZKSCAN7-AS1, ZNF35 (V226M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309330	NM_003420.4(ZNF35):c.725G>A (p.Arg242Gln)	ZKSCAN7-AS1, ZNF35 (R242Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2358343	NM_003420.4(ZNF35):c.786T>G (p.Ser262Arg)	ZKSCAN7-AS1, ZNF35 (S262R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2365289	NM_003420.4(ZNF35):c.1019G>A (p.Gly340Glu)	ZKSCAN7-AS1, ZNF35 (G340E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2600696	NM_003420.4(ZNF35):c.1133T>C (p.Ile378Thr)	ZKSCAN7-AS1, ZNF35 (I378T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2473306	NM_003420.4(ZNF35):c.1264G>A (p.Glu422Lys)	ZKSCAN7-AS1, ZNF35 (E422K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2319509	NM_003420.4(ZNF35):c.1300A>C (p.Ile434Leu)	ZKSCAN7-AS1, ZNF35 (I434L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2490435	NM_003420.4(ZNF35):c.1407T>G (p.Asn469Lys)	ZKSCAN7-AS1, ZNF35 (N469K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2507870	NM_003420.4(ZNF35):c.1567A>G (p.Thr523Ala)	ZKSCAN7-AS1, ZNF35 (T523A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance