"PreventionGenetics, part of Exact Sciences"[submitter] AND "PPP2CA"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039371	NM_002715.4(PPP2CA):c.5_6del	PPP2CA	Deletion (3 prime UTR variant +1 more)	PPP2CA-related disorder	GLikely benign
Select item 2631335	NM_002715.4(PPP2CA):c.796T>C (p.Cys266Arg)	PPP2CA (C201R +1 more)	Single nucleotide variant (missense variant +1 more)	PPP2CA-related disorder	GLikely pathogenic
Select item 2633346	NM_002715.4(PPP2CA):c.654C>A (p.Tyr218Ter)	PPP2CA (Y153* +1 more)	Single nucleotide variant (nonsense +1 more)	PPP2CA-related disorder	GLikely pathogenic
Select item 2637191	NM_002715.4(PPP2CA):c.575A>C (p.Glu192Ala)	PPP2CA (E127A +1 more)	Single nucleotide variant (missense variant +1 more)	PPP2CA-related disorder	GUncertain significance
Select item 3055175	NM_002715.4(PPP2CA):c.305C>T (p.Ala102Val)	PPP2CA (A102V +1 more)	Single nucleotide variant (missense variant +1 more)	PPP2CA-related disorder	GLikely benign
Select item 1625452	NM_002715.4(PPP2CA):c.180G>A (p.Gly60=)	PPP2CA	Single nucleotide variant (5 prime UTR variant +2 more)	PPP2CA-related disorder +1 more	GLikely benign

ClinVar