"Ambry Genetics"[submitter] AND "PPP3CB"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3217807	NM_021132.4(PPP3CB):c.1525A>G (p.Thr509Ala)	PPP3CB (T500A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611033	NM_021132.4(PPP3CB):c.1492G>T (p.Ala498Ser)	PPP3CB (A498S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265665	NM_021132.4(PPP3CB):c.1381A>G (p.Ile461Val)	PPP3CB (I461V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208224	NM_021132.4(PPP3CB):c.261G>A (p.Met87Ile)	PPP3CB (M87I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528292	NM_021132.4(PPP3CB):c.154G>A (p.Val52Ile)	PPP3CB (V52I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596345	NM_021132.4(PPP3CB):c.140A>T (p.Asp47Val)	PPP3CB (D47V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536603	NM_021132.4(PPP3CB):c.64G>A (p.Gly22Arg)	LOC130004079, PPP3CB +1 more (G22R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar