R57T (p.Arg57Thr) variant of IL2RA (P01589)
R57T (p.Arg57Thr) 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.
R57T (p.Arg57Thr) variant details
- p.Arg57Thr
- NCI-TCGA Cosmic COSV5691
- cosmic curated COSV56919
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available