"PreventionGenetics, part of Exact Sciences"[submitter] AND "PRKAA2"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056337	NM_006252.4(PRKAA2):c.111A>G (p.Leu37=)	PRKAA2	Single nucleotide variant (synonymous variant)	PRKAA2-related condition	GBenign
Select item 3043336	NM_006252.4(PRKAA2):c.728C>T (p.Thr243Ile)	PRKAA2 (T243I)	Single nucleotide variant (missense variant)	PRKAA2-related condition	GLikely benign
Select item 3039233	NM_006252.4(PRKAA2):c.749A>G (p.Gln250Arg)	PRKAA2 (Q250R)	Single nucleotide variant (missense variant)	PRKAA2-related condition	GLikely benign
Select item 730280	NM_006252.4(PRKAA2):c.789-4C>T	PRKAA2	Single nucleotide variant (intron variant)	PRKAA2-related condition +1 more	GBenign/Likely benign
Select item 779398	NM_006252.4(PRKAA2):c.939T>C (p.Ser313=)	PRKAA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3053540	NM_006252.4(PRKAA2):c.1563C>T (p.Thr521=)	PRKAA2	Single nucleotide variant (synonymous variant)	PRKAA2-related condition	GLikely benign

ClinVar