L141V (p.Leu141Val) variant of SLC2A2 (P11168)
L141V (p.Leu141Val) 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.
L141V (p.Leu141Val) variant details
- p.Leu141Val
- NCI-TCGA Cosmic COSV1000
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available