P38S (p.Pro38Ser) variant of CD79B (P40259)
P38S (p.Pro38Ser) in CD79B (P40259) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not specified. The record also includes structural context.
P38S (p.Pro38Ser) variant details
- p.Pro38Ser
- cosmic curated COSV50077
- Uncertain significance
- not specified
- Missense
- ClinVar: Uncertain significance (not specified)
- UniProt: Uncertain significance
- Structural context available