C2931787[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 41047	NM_002734.5(PRKAR1A):c.87G>A (p.Ala29=)	PRKAR1A	Single nucleotide variant (synonymous variant)	not provided +6 more	GBenign/Likely benign
Select item 413781	NM_002734.5(PRKAR1A):c.156A>G (p.Glu52=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 41044	NM_002734.5(PRKAR1A):c.204G>A (p.Leu68=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Pigmented nodular adrenocortical disease, primary, 1 +6 more	GBenign/Likely benign
Select item 378429	NM_002734.5(PRKAR1A):c.440+15T>C	PRKAR1A	Single nucleotide variant (intron variant)	Carney complex, type 1 +3 more	GBenign
Select item 413784	NM_002734.5(PRKAR1A):c.489T>C (p.Thr163=)	PRKAR1A	Single nucleotide variant (synonymous variant)	Familial atrial myxoma +5 more	GBenign/Likely benign
Select item 413791	NM_002734.5(PRKAR1A):c.549+10A>C	PRKAR1A	Single nucleotide variant (intron variant)	Familial atrial myxoma +2 more	GLikely benign
Select item 413787	NM_002734.5(PRKAR1A):c.770-9G>T	PRKAR1A	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 239381	NM_002734.5(PRKAR1A):c.1029C>T (p.Gly343=)	PRKAR1A	Single nucleotide variant (synonymous variant +1 more)	Carney complex, type 1 +4 more	GBenign/Likely benign

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