D39G (p.Asp39Gly) variant of IL2RG (P31785)
D39G (p.Asp39Gly) in IL2RG (P31785) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in XSCID. The record also includes structural context.
D39G (p.Asp39Gly) variant details
- p.Asp39Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- in XSCID
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in XSCID)
- Structural context available