List of variants in gene PRKAR1A reported as likely benign for not provided

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_002734.5(PRKAR1A):c.87G>A (p.Ala29=)	rs3730349	0.01815
NM_002734.5(PRKAR1A):c.*1837G>T	rs201999343	0.01775
NM_002734.5(PRKAR1A):c.-6-312C>T	rs114670810	0.01345
NM_002734.5(PRKAR1A):c.549+233C>T	rs151262170	0.01272
NM_002734.5(PRKAR1A):c.770-154A>G	rs3730369	0.01255
NM_002734.5(PRKAR1A):c.891+269C>T	rs147647032	0.01248
NM_002734.5(PRKAR1A):c.502+26T>C	rs76608451	0.01149
NM_212471.3(PRKAR1A):c.-7+91G>T	rs78919109	0.01118
NM_002734.5(PRKAR1A):c.*138C>A	rs28730842	0.00772
NM_002734.5(PRKAR1A):c.550-234T>C	rs76534120	0.00713
NM_002734.5(PRKAR1A):c.*759C>T	rs62087489	0.00683
NM_002734.5(PRKAR1A):c.892-126A>C	rs79109160	0.00602
NM_002734.5(PRKAR1A):c.204G>A (p.Leu68=)	rs74863634	0.00405
NM_002734.5(PRKAR1A):c.*151A>G	rs11540571	0.00340
NM_002734.5(PRKAR1A):c.1029C>T (p.Gly343=)	rs1803241	0.00265
NM_002734.5(PRKAR1A):c.678C>T (p.Ile226=)	rs200592054	0.00026
NM_002734.5(PRKAR1A):c.489T>C (p.Thr163=)	rs143672551	0.00021
NM_002734.5(PRKAR1A):c.381T>C (p.Ala127=)	rs372669687	0.00011
NM_002734.5(PRKAR1A):c.974-10C>T	rs774715675	0.00007
NM_002734.5(PRKAR1A):c.552C>G (p.Val184=)	rs751501857	0.00005
NM_002734.5(PRKAR1A):c.546G>A (p.Thr182=)	rs117639566	0.00004
NM_002734.5(PRKAR1A):c.762T>C (p.Ser254=)	rs753621663	0.00003
NM_002734.5(PRKAR1A):c.1083A>G (p.Pro361=)	rs766529889	0.00001
NM_002734.5(PRKAR1A):c.440+7A>G	rs377133184	0.00001
NM_002734.5(PRKAR1A):c.502+14G>C	rs755262664	0.00001
NM_002734.5(PRKAR1A):c.717A>C (p.Thr239=)	rs138919971	0.00001
NM_002734.5(PRKAR1A):c.246T>A (p.Ile82=)
NM_002734.5(PRKAR1A):c.42C>T (p.Ser14=)	rs2143149658
NM_002734.5(PRKAR1A):c.441-5del	rs777677808
NM_002734.5(PRKAR1A):c.503-13dup	rs138285568

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