"Ambry Genetics"[submitter] AND "GPR35"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2615793	NM_005301.5(GPR35):c.77A>T (p.Tyr26Phe)	GPR35 (Y57F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2367305	NM_005301.5(GPR35):c.188C>T (p.Ala63Val)	LOC122889014, GPR35 (A63V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2478255	NM_005301.5(GPR35):c.200T>C (p.Leu67Pro)	GPR35, LOC122889014 (L98P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2558603	NM_005301.5(GPR35):c.275C>T (p.Ser92Phe)	LOC122889014, GPR35 (S92F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2280245	NM_005301.5(GPR35):c.287A>T (p.Tyr96Phe)	LOC122889014, GPR35 (Y127F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2325630	NM_005301.5(GPR35):c.334G>A (p.Val112Met)	GPR35, LOC122889014 (V112M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2391273	NM_005301.5(GPR35):c.352G>A (p.Val118Met)	LOC122889014, GPR35 (V118M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2512443	NM_005301.5(GPR35):c.362C>T (p.Pro121Leu)	GPR35, LOC122889014 (P152L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351613	NM_005301.5(GPR35):c.367C>T (p.Arg123Cys)	LOC122889014, GPR35 (R123C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2366118	NM_005301.5(GPR35):c.401C>T (p.Ala134Val)	LOC122889014, GPR35 (A165V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2461487	NM_005301.5(GPR35):c.499C>T (p.Arg167Trp)	GPR35 (R167W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2612235	NM_005301.5(GPR35):c.527C>T (p.Pro176Leu)	GPR35 (P176L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2485845	NM_005301.5(GPR35):c.584T>C (p.Val195Ala)	GPR35 (V195A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2251439	NM_005301.5(GPR35):c.703G>T (p.Val235Leu)	GPR35 (V235L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2382579	NM_005301.5(GPR35):c.724G>A (p.Ala242Thr)	GPR35 (A242T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2288977	NM_005301.5(GPR35):c.766C>T (p.Arg256Cys)	GPR35 (R287C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2395912	NM_005301.5(GPR35):c.767G>A (p.Arg256His)	GPR35 (R256H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2239085	NM_005301.5(GPR35):c.917T>A (p.Val306Glu)	GPR35 (V306E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance