"Ambry Genetics"[submitter] AND "PSMA4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2302401	NM_002789.6(PSMA4):c.278T>G (p.Ile93Ser)	PSMA4 (I22S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320846	NM_002789.6(PSMA4):c.503G>A (p.Ser168Asn)	PSMA4 (S137N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490495	NM_002789.6(PSMA4):c.574T>G (p.Leu192Val)	PSMA4 (L121V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220347	NM_002789.6(PSMA4):c.698T>C (p.Val233Ala)	PSMA4 (V233A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519757	NM_002789.6(PSMA4):c.715A>C (p.Lys239Gln)	PSMA4 (K168Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297720	NM_002789.6(PSMA4):c.724G>A (p.Glu242Lys)	PSMA4 (E242K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar