S69T (p.Ser69Thr) variant of CD79B (P40259)
S69T (p.Ser69Thr) 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.
S69T (p.Ser69Thr) variant details
- p.Ser69Thr
- NCI-TCGA Cosmic COSV5007
- cosmic curated COSV50076
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available