S41T (p.Ser41Thr) variant of CD79B (P40259)
S41T (p.Ser41Thr) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data and structural context.
S41T (p.Ser41Thr) variant details
- p.Ser41Thr
- gnomAD rs1286736249
- Missense
- Variant Prioritization Score for Impact Estimate 0.168
- REVEL 0.09
- CADD 14.20
- PolyPhen-2 0.03
- SIFT 0.19
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available