"Ambry Genetics"[submitter] AND "PLSCR2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2358597	NM_001395437.1(PLSCR2):c.619G>A (p.Val207Met)	PLSCR2 (V276M +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2611531	NM_001395437.1(PLSCR2):c.362T>A (p.Val121Asp)	PLSCR2 (V190D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2393612	NM_001395437.1(PLSCR2):c.211C>T (p.Arg71Trp)	PLSCR2 (R144W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2622535	NM_001395437.1(PLSCR2):c.208G>A (p.Gly70Arg)	PLSCR2 (G139R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2346753	NM_001395437.1(PLSCR2):c.101T>G (p.Val34Gly)	PLSCR2 (V107G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2561614	NM_001395437.1(PLSCR2):c.32C>T (p.Pro11Leu)	PLSCR2 (P80L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar