G41W (p.Gly41Trp) variant of SLC2A10 (O95528)
G41W (p.Gly41Trp) in SLC2A10 (O95528) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
G41W (p.Gly41Trp) variant details
- p.Gly41Trp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available