F113L (p.Phe113Leu) variant of SLC2A2 (P11168)
F113L (p.Phe113Leu) in SLC2A2 (P11168) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F113L (p.Phe113Leu) variant details
- p.Phe113Leu
- NCI-TCGA Cosmic COSV5858
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available