W76G (p.Trp76Gly) variant of IL2RA (P01589)
W76G (p.Trp76Gly) in IL2RA (P01589) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
W76G (p.Trp76Gly) variant details
- p.Trp76Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available