P78T (p.Pro78Thr) variant of SLC2A2 (P11168)
P78T (p.Pro78Thr) 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.
P78T (p.Pro78Thr) variant details
- p.Pro78Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available