F127L (p.Phe127Leu) variant of IL2RB (P14784)
F127L (p.Phe127Leu) in IL2RB (P14784) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
F127L (p.Phe127Leu) variant details
- p.Phe127Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.