S145L (p.Ser145Leu) variant of SLC2A2 (P11168)
S145L (p.Ser145Leu) 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.
S145L (p.Ser145Leu) variant details
- p.Ser145Leu
- NCI-TCGA Cosmic COSV5858
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available