R13R (p.Arg13Arg) variant of GNAS (P63092)
R13R (p.Arg13Arg) in GNAS (P63092) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
R13R (p.Arg13Arg) variant details
- p.Arg13Arg
- gnomAD 20-58840115-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.117
- CADD 5.11
- Most common in the Finnish in Finland (FIN) population (allele frequency 2e-05)
- Structural context available
- Literature evidence available