A17D (p.Ala17Asp) variant of SLC2A2 (P11168)
A17D (p.Ala17Asp) 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.
A17D (p.Ala17Asp) variant details
- p.Ala17Asp
- NCI-TCGA Cosmic COSV1000
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available