ClinVar Miner

List of variants in gene PRKAR1A reported as uncertain significance for not provided

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Total variants: 30
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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.596G>A (p.Ser199Asn) rs755798109 0.00006
NM_002734.5(PRKAR1A):c.798G>A (p.Thr266=) rs201774040 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.1075C>G (p.Leu359Val) rs2143391287
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.503-10C>A rs1555813804
NM_002734.5(PRKAR1A):c.530T>C (p.Ile177Thr) rs587778626
NM_002734.5(PRKAR1A):c.534T>G (p.Asp178Glu) rs2085739503
NM_002734.5(PRKAR1A):c.549+6A>T rs780068318
NM_002734.5(PRKAR1A):c.567A>C (p.Glu189Asp) rs767405408
NM_002734.5(PRKAR1A):c.62A>G (p.Tyr21Cys) rs2143150295
NM_002734.5(PRKAR1A):c.647A>G (p.Lys216Arg) rs1555814093
NM_002734.5(PRKAR1A):c.797C>A (p.Thr266Lys)
NM_002734.5(PRKAR1A):c.854A>G (p.Gln285Arg) rs1555814719
NM_002734.5(PRKAR1A):c.856_873del (p.Gly286_Glu291del) rs2085879368

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