R57W (p.Arg57Trp) variant of CD79B (P40259)
R57W (p.Arg57Trp) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
R57W (p.Arg57Trp) variant details
- p.Arg57Trp
- cosmic curated COSV50083
- 1000Genomes rs375597674
- ESP rs375597674
- ExAC rs375597674
- Missense
- Variant Prioritization Score for Impact Estimate 0.464
- REVEL 0.50
- CADD 24.60
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the HGDP:HEZHEN population (allele frequency 0.062)
- Structural context available