"Ambry Genetics"[submitter] AND "PSCA"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3220127	NM_005672.5(PSCA):c.22C>T (p.Pro8Ser)	PSCA (P8S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310814	NM_005672.5(PSCA):c.26G>A (p.Gly9Asp)	PSCA (G9D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600354	NM_005672.5(PSCA):c.66C>A (p.Ser22Arg)	PSCA (S22R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220126	NM_005672.5(PSCA):c.104T>G (p.Leu35Arg)	PSCA (L35R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273165	NM_005672.5(PSCA):c.120G>C (p.Trp40Cys)	PSCA (W40C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487578	NM_005672.5(PSCA):c.242A>C (p.Asp81Ala)	PSCA (D81A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540605	NM_005672.5(PSCA):c.253G>A (p.Ala85Thr)	PSCA (A85T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320216	NM_005672.5(PSCA):c.275A>T (p.Gln92Leu)	PSCA (Q92L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321625	NM_005672.5(PSCA):c.302T>C (p.Leu101Pro)	PSCA (L101P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365919	NM_005672.5(PSCA):c.334G>A (p.Gly112Ser)	PSCA (G112S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign