S78P (p.Ser78Pro) variant of IL2RG (P31785)
S78P (p.Ser78Pro) 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.
S78P (p.Ser78Pro) variant details
- p.Ser78Pro
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available