P38L (p.Pro38Leu) variant of CD79B (P40259)
P38L (p.Pro38Leu) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
P38L (p.Pro38Leu) variant details
- p.Pro38Leu
- TOPMed rs1015311105
- gnomAD rs1015311105
- Missense
- Variant Prioritization Score for Impact Estimate 0.124
- REVEL 0.13
- CADD 7.32
- PolyPhen-2 0.12
- SIFT 0.31
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available