P58T (p.Pro58Thr) variant of IL2RG (P31785)
P58T (p.Pro58Thr) in IL2RG (P31785) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P58T (p.Pro58Thr) variant details
- p.Pro58Thr
- NCI-TCGA Cosmic COSV5214
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available