R13M (p.Arg13Met) variant of GNAS (P63092)
R13M (p.Arg13Met) in GNAS (P63092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data, published literature, and structural context.
R13M (p.Arg13Met) variant details
- p.Arg13Met
- gnomAD 20-58840117-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.77
- CADD 27.80
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available