T13A (p.Thr13Ala) variant of SLC2A2 (P11168)
T13A (p.Thr13Ala) 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.
T13A (p.Thr13Ala) variant details
- p.Thr13Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available