G58D (p.Gly58Asp) variant of CD79B (P40259)
G58D (p.Gly58Asp) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data, published literature, and structural context.
G58D (p.Gly58Asp) variant details
- p.Gly58Asp
- gnomAD 17-63930331-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.427
- REVEL 0.37
- CADD 19.40
- PolyPhen-2 0.14
- SIFT 0.38
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available