T9P (p.Thr9Pro) variant of SLC2A2 (P11168)
T9P (p.Thr9Pro) in SLC2A2 (P11168) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes population frequency data and structural context.
T9P (p.Thr9Pro) variant details
- p.Thr9Pro
- rs766082034
- NCI-TCGA Cosmic COSV5858
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Population evidence available
- Structural context available