"Ambry Genetics"[submitter] AND "GPRASP3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2562015	NM_001142524.2(GPRASP3):c.98T>G (p.Val33Gly)	ARMCX5-GPRASP2, GPRASP3 (V33G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2523415	NM_001142524.2(GPRASP3):c.356T>C (p.Ile119Thr)	ARMCX5-GPRASP2, GPRASP3 (I119T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488143	NM_001142524.2(GPRASP3):c.739A>G (p.Ile247Val)	ARMCX5-GPRASP2, GPRASP3 (I247V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2522135	NM_001142524.2(GPRASP3):c.814C>G (p.Arg272Gly)	ARMCX5-GPRASP2, GPRASP3 (R272G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488144	NM_001142524.2(GPRASP3):c.932C>T (p.Ala311Val)	ARMCX5-GPRASP2, GPRASP3 (A311V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2462435	NM_001142524.2(GPRASP3):c.1006A>G (p.Thr336Ala)	GPRASP3, ARMCX5-GPRASP2 (T336A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2522681	NM_001142524.2(GPRASP3):c.1637C>G (p.Thr546Arg)	ARMCX5-GPRASP2, GPRASP3 (T546R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

ClinVar