"Ambry Genetics"[submitter] AND "GPR162"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2519461	NM_019858.2(GPR162):c.17C>T (p.Ala6Val)	GPR162 (A6V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2312051	NM_019858.2(GPR162):c.40C>A (p.Arg14Ser)	GPR162 (R14S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2552806	NM_019858.2(GPR162):c.73C>T (p.Leu25Phe)	GPR162 (L25F)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2262403	NM_019858.2(GPR162):c.245A>G (p.Asp82Gly)	GPR162 (D82G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2540124	NM_019858.2(GPR162):c.358C>T (p.Arg120Cys)	GPR162 (R120C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2259391	NM_019858.2(GPR162):c.692G>A (p.Gly231Glu)	GPR162 (G231E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2370632	NM_019858.2(GPR162):c.893C>T (p.Ser298Leu)	GPR162 (S298L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2233165	NM_019858.2(GPR162):c.1072G>A (p.Asp358Asn)	GPR162 (D358N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2494731	NM_019858.2(GPR162):c.1253A>T (p.Asn418Ile)	GPR162 (N418I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2311479	NM_019858.2(GPR162):c.1340G>A (p.Arg447Gln)	GPR162 (R163Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332813	NM_019858.2(GPR162):c.1393G>A (p.Glu465Lys)	GPR162 (E465K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2321442	NM_019858.2(GPR162):c.1394A>C (p.Glu465Ala)	GPR162 (E181A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2391179	NM_019858.2(GPR162):c.1402G>A (p.Glu468Lys)	GPR162 (E468K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232693	NM_019858.2(GPR162):c.1423G>A (p.Gly475Arg)	GPR162 (G191R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2248238	NM_019858.2(GPR162):c.1430C>T (p.Ala477Val)	GPR162 (A193V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2566903	NM_019858.2(GPR162):c.1504C>T (p.Arg502Trp)	GPR162 (R218W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2321842	NM_019858.2(GPR162):c.1508A>C (p.Glu503Ala)	GPR162 (E219A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2342201	NM_019858.2(GPR162):c.1573C>G (p.Pro525Ala)	GPR162 (P241A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2520804	NM_019858.2(GPR162):c.1579C>T (p.Arg527Trp)	GPR162 (R527W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2379784	NM_019858.2(GPR162):c.1606C>T (p.Arg536Cys)	GPR162 (R252C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232422	NM_019858.2(GPR162):c.1612C>T (p.Leu538Phe)	GPR162 (L538F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525201	NM_019858.2(GPR162):c.1706C>G (p.Ala569Gly)	GPR162 (A569G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 22