G40V (p.Gly40Val) variant of CD79B (P40259)
G40V (p.Gly40Val) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.64 / 1. The record also includes population frequency data, published literature, and structural context.
G40V (p.Gly40Val) variant details
- p.Gly40Val
- gnomAD 17-63930385-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.636
- REVEL 0.66
- CADD 31.00
- PolyPhen-2 0.77
- SIFT 0.04
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available