V28G (p.Val28Gly) variant of SLC2A4 (P14672)
V28G (p.Val28Gly) in SLC2A4 (P14672) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
V28G (p.Val28Gly) variant details
- p.Val28Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available