G148D (p.Gly148Asp) variant of SLC2A2 (P11168)
G148D (p.Gly148Asp) in SLC2A2 (P11168) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
G148D (p.Gly148Asp) variant details
- p.Gly148Asp
- NCI-TCGA Cosmic COSV5858
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available