List of variants in gene PRKAR1A reported as 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.502+209C>T	rs2907374	0.73617
NM_002734.5(PRKAR1A):c.770-24G>A	rs2302230	0.73571
NM_212471.3(PRKAR1A):c.-47C>A	rs8080306	0.72450
NM_002734.5(PRKAR1A):c.178-234A>G	rs2952275	0.71353
NM_002734.5(PRKAR1A):c.892-34G>T	rs2302231	0.71288
NM_002734.5(PRKAR1A):c.891+332T>A	rs2907387	0.30593
NM_002734.5(PRKAR1A):c.-6-711A>G	rs9913595	0.22542
NM_002734.5(PRKAR1A):c.178-116del	rs17550507	0.20430
NM_002734.5(PRKAR1A):c.974-102A>T	rs2302233	0.19147
NM_002734.5(PRKAR1A):c.709-209G>A	rs3785905	0.14612
NM_002734.5(PRKAR1A):c.708+142A>G	rs74745979	0.14601
NM_002734.5(PRKAR1A):c.770-256C>T	rs72847794	0.14573
NM_002734.5(PRKAR1A):c.-6-236C>T	rs72847785	0.14309
NM_002734.5(PRKAR1A):c.550-18A>G	rs78094410	0.03100
NM_002734.5(PRKAR1A):c.87G>A (p.Ala29=)	rs3730349	0.01815
NM_002734.5(PRKAR1A):c.204G>A (p.Leu68=)	rs74863634	0.00405
NM_002734.5(PRKAR1A):c.1029C>T (p.Gly343=)	rs1803241	0.00265
NM_002734.5(PRKAR1A):c.550-8C>T	rs375936679	0.00034
NM_002734.5(PRKAR1A):c.678C>T (p.Ile226=)	rs200592054	0.00026
NM_002734.5(PRKAR1A):c.381T>C (p.Ala127=)	rs372669687	0.00011
NM_002734.5(PRKAR1A):c.*2934T>C
NM_002734.5(PRKAR1A):c.*812A>C	rs116996069
NM_002734.5(PRKAR1A):c.-6-4G>A	rs190803359
NM_002734.5(PRKAR1A):c.-69A>G	rs2143089534
NM_002734.5(PRKAR1A):c.349-5dup	rs3841514
NM_002734.5(PRKAR1A):c.502+117dup	rs140696489
NM_002734.5(PRKAR1A):c.503-246_503-245insGT	rs3217054
NM_002734.5(PRKAR1A):c.708+134_708+135insCT	rs10625677
NM_002734.5(PRKAR1A):c.973+54G>A
NM_212471.3(PRKAR1A):c.-7+169G>T	rs111815463

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