S41R (p.Ser41Arg) variant of CD79B (P40259)
S41R (p.Ser41Arg) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
S41R (p.Ser41Arg) variant details
- p.Ser41Arg
- gnomAD 17-63930381-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.133
- REVEL 0.12
- CADD 9.59
- PolyPhen-2 0.01
- SIFT 0.08
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available