A42G (p.Ala42Gly) variant of CD79B (P40259)
A42G (p.Ala42Gly) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data, published literature, and structural context.
A42G (p.Ala42Gly) variant details
- p.Ala42Gly
- gnomAD 17-63930379-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.302
- REVEL 0.28
- CADD 15.40
- PolyPhen-2 0.06
- SIFT 0.56
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available