List of variants in gene PRKAR1B reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001164760.2(PRKAR1B):c.537A>G (p.Gln179=)	rs145653328	0.00001
NM_001164760.2(PRKAR1B):c.254C>G (p.Thr85Ser)	rs770020244
NM_001164760.2(PRKAR1B):c.728G>A (p.Arg243His)

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