"Ambry Genetics"[submitter] AND "GPR161"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2545711	NM_001375883.1(GPR161):c.1469C>T (p.Thr490Ile)	GPR161 (T510I +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2256982	NM_001375883.1(GPR161):c.1409T>C (p.Ile470Thr)	GPR161 (I338T +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2320534	NM_001375883.1(GPR161):c.1265C>T (p.Thr422Ile)	GPR161 (T439I +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1711121	NM_001375883.1(GPR161):c.1231T>C (p.Tyr411His)	GPR161 (Y279H +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2326024	NM_001375883.1(GPR161):c.1212T>A (p.Asp404Glu)	GPR161 (D272E +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2514542	NM_001375883.1(GPR161):c.1048G>T (p.Val350Leu)	GPR161 (V272L +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2338236	NM_001375883.1(GPR161):c.947G>T (p.Ser316Ile)	GPR161 (S202I +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2346241	NM_001375883.1(GPR161):c.838A>C (p.Met280Leu)	GPR161 (M202L +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2307276	NM_001375883.1(GPR161):c.764C>T (p.Ala255Val)	GPR161 (A177V +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2272232	NM_001375883.1(GPR161):c.758G>A (p.Arg253Lys)	GPR161 (R175K +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2513722	NM_001375883.1(GPR161):c.638G>A (p.Arg213His)	GPR161 (R230H +5 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2597786	NM_001375883.1(GPR161):c.268C>T (p.Arg90Cys)	GPR161 (R90C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2228215	NM_001375883.1(GPR161):c.257C>T (p.Thr86Met)	GPR161 (T106M +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2545987	NM_001375883.1(GPR161):c.239T>C (p.Val80Ala)	GPR161 (V80A +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2277306	NM_001375883.1(GPR161):c.196G>A (p.Val66Ile)	GPR161 (V83I +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance