C46G (p.Cys46Gly) variant of IL2RB (P14784)
C46G (p.Cys46Gly) in IL2RB (P14784) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
C46G (p.Cys46Gly) variant details
- p.Cys46Gly
- NCI-TCGA Cosmic COSV5342
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.