P38H (p.Pro38His) variant of CD79B (P40259)
P38H (p.Pro38His) 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.
P38H (p.Pro38His) variant details
- p.Pro38His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available