R55G (p.Arg55Gly) variant of CD79B (P40259)
R55G (p.Arg55Gly) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data, published literature, and structural context.
R55G (p.Arg55Gly) variant details
- p.Arg55Gly
- gnomAD 17-63930341-T-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.271
- REVEL 0.18
- CADD 23.30
- PolyPhen-2 0.39
- SIFT 0.09
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available