W47R (p.Trp47Arg) variant of CD79B (P40259)
W47R (p.Trp47Arg) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data, published literature, and structural context.
W47R (p.Trp47Arg) variant details
- p.Trp47Arg
- gnomAD 17-63930365-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.23
- REVEL 0.28
- CADD 11.10
- PolyPhen-2 0.93
- SIFT 0.32
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available