"Ambry Genetics"[submitter] AND "PPP1R1C"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3217560	NM_001080545.3(PPP1R1C):c.37G>A (p.Val13Met)	PPP1R1C (V13M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269998	NM_001080545.3(PPP1R1C):c.101C>A (p.Thr34Lys)	PPP1R1C (T34K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217558	NM_001080545.3(PPP1R1C):c.125A>G (p.Asn42Ser)	PPP1R1C (N49S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620607	NM_001080545.3(PPP1R1C):c.131A>G (p.His44Arg)	PPP1R1C (H44R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217559	NM_001080545.3(PPP1R1C):c.235A>G (p.Ile79Val)	PPP1R1C (I86V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395168	NM_001080545.3(PPP1R1C):c.268G>A (p.Glu90Lys)	PPP1R1C (E97K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar