Y89F (p.Tyr89Phe) variant of IL2RG (P31785)
Y89F (p.Tyr89Phe) 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.
Y89F (p.Tyr89Phe) variant details
- p.Tyr89Phe
- NCI-TCGA Cosmic COSV5215
- Variant assessed as somatic; moderate impact.
- in XSCID
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in XSCID)
- Structural context available