G18V (p.Gly18Val) variant of SLC2A1 (P11166)
G18V (p.Gly18Val) in SLC2A1 (P11166) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G18V (p.Gly18Val) variant details
- p.Gly18Val
- NCI-TCGA Cosmic COSV1009
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available