"Ambry Genetics"[submitter] AND "WNT8A"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2454578	NM_001300939.2(WNT8A):c.-32A>G	WNT8A (N3D)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases	GLikely benign
Select item 2590439	NM_001300939.2(WNT8A):c.-5G>A	WNT8A (G12S)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2256437	NM_001300939.2(WNT8A):c.152C>A (p.Pro51His)	WNT8A (P33H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2346148	NM_001300939.2(WNT8A):c.173C>T (p.Thr58Met)	WNT8A (T58M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2332899	NM_001300939.2(WNT8A):c.197A>C (p.Gln66Pro)	WNT8A (Q66P +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2341470	NM_001300939.2(WNT8A):c.239G>T (p.Arg80Leu)	WNT8A (R62L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2402284	NM_001300939.2(WNT8A):c.384A>T (p.Glu128Asp)	WNT8A (E128D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2380812	NM_001300939.2(WNT8A):c.536A>C (p.Asn179Thr)	WNT8A (N161T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2346240	NM_001300939.2(WNT8A):c.592T>G (p.Cys198Gly)	WNT8A (C198G +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2552928	NM_001300939.2(WNT8A):c.698C>T (p.Ala233Val)	WNT8A (A215V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2369802	NM_001300939.2(WNT8A):c.748G>A (p.Glu250Lys)	WNT8A (E232K +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2232217	NM_001300939.2(WNT8A):c.757T>C (p.Trp253Arg)	WNT8A (W235R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2269392	NM_001300939.2(WNT8A):c.772G>A (p.Ala258Thr)	WNT8A (A240T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2249569	NM_001300939.2(WNT8A):c.799C>A (p.Leu267Met)	WNT8A (L249M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2330969	NM_001300939.2(WNT8A):c.872G>A (p.Arg291His)	WNT8A (R291H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2409865	NM_001300939.2(WNT8A):c.886A>T (p.Asn296Tyr)	WNT8A (N296Y +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2568601	NM_001300939.2(WNT8A):c.929G>A (p.Arg310His)	WNT8A (R292H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2517303	NM_001300939.2(WNT8A):c.1052A>G (p.Lys351Arg)	WNT8A (K351R +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance