List of variants in gene PRKAR1A reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_002734.5(PRKAR1A):c.914G>A (p.Arg305His)	rs768253469	0.00010
NM_002734.5(PRKAR1A):c.1024C>T (p.Arg342Cys)	rs146383819	0.00006
NM_002734.5(PRKAR1A):c.1042G>A (p.Val348Ile)	rs772571340	0.00006
NM_002734.5(PRKAR1A):c.139A>G (p.Met47Val)	rs548529083	0.00003
NM_002734.5(PRKAR1A):c.19G>A (p.Ala7Thr)	rs369210646	0.00003
NM_002734.5(PRKAR1A):c.756A>C (p.Lys252Asn)	rs1242606073	0.00003
NM_002734.5(PRKAR1A):c.220C>T (p.Arg74Cys)	rs137853303	0.00002
NM_002734.5(PRKAR1A):c.260C>T (p.Pro87Leu)	rs1165953688	0.00001
NM_002734.5(PRKAR1A):c.790C>T (p.Arg264Cys)	rs2085877268	0.00001
NM_002734.5(PRKAR1A):c.-6-1G>A
NM_002734.5(PRKAR1A):c.1118A>C (p.Tyr373Ser)
NM_002734.5(PRKAR1A):c.180G>A (p.Glu60=)
NM_002734.5(PRKAR1A):c.300C>T (p.Ile100=)	rs778361747
NM_002734.5(PRKAR1A):c.35C>G (p.Ala12Gly)	rs1292133703
NM_002734.5(PRKAR1A):c.440+5G>A	rs1555813456
NM_002734.5(PRKAR1A):c.441-5T>G	rs771949207
NM_002734.5(PRKAR1A):c.502+3A>C	rs1600482167
NM_002734.5(PRKAR1A):c.62A>G (p.Tyr21Cys)	rs2143150295
NM_002734.5(PRKAR1A):c.797C>A (p.Thr266Lys)

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