"Ambry Genetics"[submitter] AND "PSMA3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1387811	NM_002788.4(PSMA3):c.214C>T (p.Arg72Trp)	PSMA3 (R72W)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2484001	NM_002788.4(PSMA3):c.365C>T (p.Ala122Val)	PSMA3 (A122V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2315669	NM_002788.4(PSMA3):c.368A>G (p.Tyr123Cys)	PSMA3 (Y123C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2220845	NM_002788.4(PSMA3):c.436G>A (p.Gly146Ser)	PSMA3 (G139S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1353276	NM_002788.4(PSMA3):c.694A>G (p.Ile232Val)	PSMA3, PSMA3-AS1 (I225V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 1017428	NM_002788.4(PSMA3):c.741A>T (p.Glu247Asp)	PSMA3, PSMA3-AS1 (E240D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance

ClinVar