R139K (p.Arg139Lys) variant of IL2RG (P31785)
R139K (p.Arg139Lys) 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.
R139K (p.Arg139Lys) variant details
- p.Arg139Lys
- NCI-TCGA Cosmic COSV5214
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available