F59S (p.Phe59Ser) variant of CD79B (P40259)
F59S (p.Phe59Ser) in CD79B (P40259) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F59S (p.Phe59Ser) variant details
- p.Phe59Ser
- NCI-TCGA Cosmic COSV5007
- cosmic curated COSV50079
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available