P79H (p.Pro79His) variant of WAS (P42768)
P79H (p.Pro79His) 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.
P79H (p.Pro79His) variant details
- p.Pro79His
- NCI-TCGA Cosmic COSV6499
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available