L18P (p.Leu18Pro) variant of IL2RG (P31785)
L18P (p.Leu18Pro) 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.
L18P (p.Leu18Pro) variant details
- p.Leu18Pro
- NCI-TCGA Cosmic COSV5215
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available