"Ambry Genetics"[submitter] AND "PSMA8"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2382236	NM_001025096.2(PSMA8):c.19A>T (p.Arg7Trp)	PSMA8 (R7W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484940	NM_001025096.2(PSMA8):c.79G>A (p.Ala27Thr)	PSMA8 (A27T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220355	NM_001025096.2(PSMA8):c.90A>C (p.Lys30Asn)	PSMA8 (K30N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220351	NM_001025096.2(PSMA8):c.101C>T (p.Ala34Val)	PSMA8 (A34V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310954	NM_001025096.2(PSMA8):c.126A>G (p.Ile42Met)	PSMA8 (I16M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480966	NM_001025096.2(PSMA8):c.127G>C (p.Val43Leu)	PSMA8 (V17L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599387	NM_001025096.2(PSMA8):c.170A>G (p.Asp57Gly)	PSMA8 (D31G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372583	NM_001025096.2(PSMA8):c.203A>G (p.Asp68Gly)	PSMA8 (D42G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310955	NM_001025096.2(PSMA8):c.223T>G (p.Phe75Val)	PSMA8 (F49V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204290	NM_001025096.2(PSMA8):c.230-4A>G	PSMA8 (I82V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3220352	NM_001025096.2(PSMA8):c.268C>T (p.Arg90Cys)	PSMA8 (R52C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350364	NM_001025096.2(PSMA8):c.269G>C (p.Arg90Pro)	PSMA8 (R96P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220353	NM_001025096.2(PSMA8):c.275A>G (p.Glu92Gly)	PSMA8 (E92G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607117	NM_001025096.2(PSMA8):c.290A>G (p.Lys97Arg)	PSMA8 (K97R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220571	NM_001025096.2(PSMA8):c.466C>G (p.His156Asp)	PSMA8 (H162D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533695	NM_001025096.2(PSMA8):c.494G>A (p.Arg165Gln)	PSMA8 (R127Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311596	NM_001025096.2(PSMA8):c.569T>C (p.Ile190Thr)	PSMA8 (I190T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615328	NM_001025096.2(PSMA8):c.581T>G (p.Ile194Arg)	PSMA8 (I168R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324324	NM_001025096.2(PSMA8):c.647A>G (p.Asn216Ser)	PSMA8 (N190S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380228	NM_001025096.2(PSMA8):c.674A>G (p.Lys225Arg)	PSMA8 (K225R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 20