S69R (p.Ser69Arg) variant of CD79B (P40259)
S69R (p.Ser69Arg) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
S69R (p.Ser69Arg) variant details
- p.Ser69Arg
- gnomAD 17-63930297-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.162
- REVEL 0.20
- CADD 5.75
- PolyPhen-2 0.14
- SIFT 0.25
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available