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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2287087	NM_002730.4(PRKACA):c.879G>T (p.Lys293Asn)	PRKACA (K369N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237913	NM_002730.4(PRKACA):c.859A>G (p.Asn287Asp)	PRKACA (N287D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541259	NM_002730.4(PRKACA):c.790T>C (p.Ser264Pro)	PRKACA (S264P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332237	NM_002730.4(PRKACA):c.591G>T (p.Trp197Cys)	PRKACA (W197C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218708	NM_002730.4(PRKACA):c.532C>A (p.Gln178Lys)	PRKACA (Q254K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553520	NM_002730.4(PRKACA):c.185A>G (p.Lys62Arg)	PRKACA (K54R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar