List of variants in gene PRKAR1A reported as benign for Hereditary cancer-predisposing syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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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.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.489T>C (p.Thr163=)	rs143672551	0.00021
NM_002734.5(PRKAR1A):c.330G>A (p.Ala110=)	rs371834376	0.00016
NM_002734.5(PRKAR1A):c.156A>G (p.Glu52=)	rs141432364	0.00012
NM_002734.5(PRKAR1A):c.483A>G (p.Gly161=)	rs141518491	0.00011
NM_002734.5(PRKAR1A):c.103A>G (p.Ile35Val)	rs377513504	0.00009
NM_002734.5(PRKAR1A):c.63C>T (p.Tyr21=)	rs777110464	0.00001
NM_002734.5(PRKAR1A):c.349-5dup	rs3841514
NM_002734.5(PRKAR1A):c.567A>C (p.Glu189Asp)	rs767405408

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