P38A (p.Pro38Ala) variant of CD79B (P40259)
P38A (p.Pro38Ala) in CD79B (P40259) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
P38A (p.Pro38Ala) variant details
- p.Pro38Ala
- TOPMed rs1908110755
- gnomAD rs1908110755
- Missense
- Variant Prioritization Score for Impact Estimate 0.111
- REVEL 0.15
- CADD 0.54
- PolyPhen-2 0.08
- SIFT 0.23
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available