A29V (p.Ala29Val) variant of CD79B (P40259)
A29V (p.Ala29Val) in CD79B (P40259) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
A29V (p.Ala29Val) variant details
- p.Ala29Val
- NCI-TCGA TCGA novel
- TOPMed rs1908116871
- gnomAD rs1908116871
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.143
- REVEL 0.12
- CADD 12.40
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available