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

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Items: 33

	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)	not specified	GUncertain significance
Select item 3101728	NM_005301.5(GPR35):c.115A>G (p.Ser39Gly)	GPR35 (S39G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2367305	NM_005301.5(GPR35):c.188C>T (p.Ala63Val)	GPR35, LOC122889014 (A63V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478255	NM_005301.5(GPR35):c.200T>C (p.Leu67Pro)	GPR35, LOC122889014 (L98P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101730	NM_005301.5(GPR35):c.257C>T (p.Thr86Met)	GPR35, LOC122889014 (T117M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282381	NM_005301.5(GPR35):c.260C>T (p.Pro87Leu)	GPR35, LOC122889014 (P87L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2558603	NM_005301.5(GPR35):c.275C>T (p.Ser92Phe)	GPR35, LOC122889014 (S92F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280245	NM_005301.5(GPR35):c.287A>T (p.Tyr96Phe)	GPR35, LOC122889014 (Y127F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101731	NM_005301.5(GPR35):c.312C>G (p.Ile104Met)	GPR35, LOC122889014 (I104M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325630	NM_005301.5(GPR35):c.334G>A (p.Val112Met)	GPR35, LOC122889014 (V112M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391273	NM_005301.5(GPR35):c.352G>A (p.Val118Met)	GPR35, LOC122889014 (V118M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512443	NM_005301.5(GPR35):c.362C>T (p.Pro121Leu)	GPR35, LOC122889014 (P152L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351613	NM_005301.5(GPR35):c.367C>T (p.Arg123Cys)	GPR35, LOC122889014 (R123C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366118	NM_005301.5(GPR35):c.401C>T (p.Ala134Val)	GPR35, LOC122889014 (A165V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101732	NM_005301.5(GPR35):c.406G>A (p.Val136Met)	GPR35, LOC122889014 (V136M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101733	NM_005301.5(GPR35):c.412G>A (p.Ala138Thr)	GPR35, LOC122889014 (A138T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461487	NM_005301.5(GPR35):c.499C>T (p.Arg167Trp)	GPR35 (R167W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612235	NM_005301.5(GPR35):c.527C>T (p.Pro176Leu)	GPR35 (P176L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101734	NM_005301.5(GPR35):c.556G>A (p.Val186Met)	GPR35 (V186M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282382	NM_005301.5(GPR35):c.583G>T (p.Val195Leu)	GPR35 (V195L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485845	NM_005301.5(GPR35):c.584T>C (p.Val195Ala)	GPR35 (V195A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101735	NM_005301.5(GPR35):c.649C>T (p.Arg217Cys)	GPR35 (R217C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101736	NM_005301.5(GPR35):c.698T>C (p.Leu233Pro)	GPR35 (L264P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251439	NM_005301.5(GPR35):c.703G>T (p.Val235Leu)	GPR35 (V235L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101739	NM_005301.5(GPR35):c.718C>T (p.Arg240Cys)	GPR35 (R240C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101738	NM_005301.5(GPR35):c.718C>A (p.Arg240Ser)	GPR35 (R240S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101740	NM_005301.5(GPR35):c.719G>T (p.Arg240Leu)	GPR35 (R271L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382579	NM_005301.5(GPR35):c.724G>A (p.Ala242Thr)	GPR35 (A242T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282383	NM_005301.5(GPR35):c.764G>A (p.Arg255His)	GPR35 (R255H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288977	NM_005301.5(GPR35):c.766C>T (p.Arg256Cys)	GPR35 (R287C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395912	NM_005301.5(GPR35):c.767G>A (p.Arg256His)	GPR35 (R256H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101741	NM_005301.5(GPR35):c.881G>A (p.Ser294Asn)	GPR35 (S294N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239085	NM_005301.5(GPR35):c.917T>A (p.Val306Glu)	GPR35 (V306E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 33