G111C (p.Gly111Cys) variant of SLC2A1 (P11166)
G111C (p.Gly111Cys) 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.
G111C (p.Gly111Cys) variant details
- p.Gly111Cys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available