R88G (p.Arg88Gly) variant of IL2RA (P01589)
R88G (p.Arg88Gly) 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.
R88G (p.Arg88Gly) variant details
- p.Arg88Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available