V69A (p.Val69Ala) variant of CD79A (P11912)
V69A (p.Val69Ala) in CD79A (P11912) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V69A (p.Val69Ala) variant details
- p.Val69Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available