C69F (p.Cys69Phe) variant of WAS (P42768)
C69F (p.Cys69Phe) in WAS (P42768) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C69F (p.Cys69Phe) variant details
- p.Cys69Phe
- NCI-TCGA Cosmic COSV1009
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available