G17A (p.Gly17Ala) variant of SLC2A1 (P11166)
G17A (p.Gly17Ala) 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.
G17A (p.Gly17Ala) variant details
- p.Gly17Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available