"Ambry Genetics"[submitter] AND "WDR88"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3333000	NM_173479.4(WDR88):c.79G>A (p.Glu27Lys)	WDR88 (E27K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379932	NM_173479.4(WDR88):c.91G>A (p.Gly31Ser)	WDR88 (G31S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190359	NM_173479.4(WDR88):c.159C>G (p.His53Gln)	WDR88 (H53Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190360	NM_173479.4(WDR88):c.306G>C (p.Glu102Asp)	WDR88 (E102D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233452	NM_173479.4(WDR88):c.307C>T (p.His103Tyr)	WDR88 (H103Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190361	NM_173479.4(WDR88):c.318C>A (p.Ser106Arg)	WDR88 (S106R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312126	NM_173479.4(WDR88):c.367G>C (p.Asp123His)	WDR88 (D123H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325577	NM_173479.4(WDR88):c.614T>G (p.Phe205Cys)	WDR88 (F205C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485150	NM_173479.4(WDR88):c.631A>G (p.Ile211Val)	WDR88 (I211V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3332998	NM_173479.4(WDR88):c.649G>A (p.Glu217Lys)	WDR88 (E217K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279094	NM_173479.4(WDR88):c.791C>T (p.Thr264Met)	LOC132090907, WDR88 (T264M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190363	NM_173479.4(WDR88):c.821A>G (p.Asn274Ser)	WDR88 (N274S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190364	NM_173479.4(WDR88):c.958C>T (p.His320Tyr)	WDR88 (H320Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370134	NM_173479.4(WDR88):c.1016G>A (p.Gly339Glu)	WDR88 (G339E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311253	NM_173479.4(WDR88):c.1024G>C (p.Asp342His)	WDR88 (D342H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359111	NM_173479.4(WDR88):c.1104T>A (p.Asp368Glu)	WDR88 (D368E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362666	NM_173479.4(WDR88):c.1132A>G (p.Ile378Val)	WDR88 (I378V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2326442	NM_173479.4(WDR88):c.1151A>G (p.Asp384Gly)	WDR88 (D384G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337056	NM_173479.4(WDR88):c.1311C>G (p.Cys437Trp)	WDR88 (C437W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190356	NM_173479.4(WDR88):c.1319G>C (p.Cys440Ser)	WDR88 (C440S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190357	NM_173479.4(WDR88):c.1336G>T (p.Gly446Cys)	WDR88 (G446C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321634	NM_173479.4(WDR88):c.1336G>A (p.Gly446Ser)	WDR88 (G446S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359460	NM_173479.4(WDR88):c.1343C>T (p.Pro448Leu)	WDR88 (P448L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190358	NM_173479.4(WDR88):c.1352C>T (p.Thr451Ile)	WDR88 (T451I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24