"Ambry Genetics"[submitter] AND "PSMA1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2485952	NM_002786.4(PSMA1):c.671A>G (p.Tyr224Cys)	PSMA1 (Y230C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527696	NM_002786.4(PSMA1):c.498A>T (p.Gln166His)	PSMA1 (Q172H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559707	NM_002786.4(PSMA1):c.481A>G (p.Ile161Val)	PSMA1 (I167V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561037	NM_002786.4(PSMA1):c.298G>A (p.Asp100Asn)	PSMA1 (D106N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620564	NM_002786.4(PSMA1):c.266G>T (p.Arg89Leu)	PSMA1 (R95L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310949	NM_002786.4(PSMA1):c.220A>G (p.Ile74Val)	PSMA1 (I80V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245821	NM_002786.4(PSMA1):c.208A>G (p.Ile70Val)	PSMA1 (I70V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar