"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "RALGAPA1"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3380184	NM_001346249.2(RALGAPA1):c.7459C>T (p.Arg2487Cys)	RALGAPA1 (R1981C +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3380185	NM_001346249.2(RALGAPA1):c.5807A>G (p.Tyr1936Cys)	RALGAPA1 (Y1430C +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3380186	NM_001346249.2(RALGAPA1):c.4580A>T (p.Asp1527Val)	RALGAPA1 (D1021V +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3380187	NM_001346249.2(RALGAPA1):c.1934T>C (p.Leu645Ser)	RALGAPA1 (L645S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1675538	NM_001346249.2(RALGAPA1):c.1819A>G (p.Lys607Glu)	RALGAPA1 (K607E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3380188	NM_001346249.2(RALGAPA1):c.1692T>G (p.Ile564Met)	RALGAPA1 (I564M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

ClinVar