P118L (p.Pro118Leu) variant of IDH2 (P48735)
P118L (p.Pro118Leu) in IDH2 (P48735) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
P118L (p.Pro118Leu) variant details
- p.Pro118Leu
- NCI-TCGA Cosmic COSV1003
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available