G39V (p.Gly39Val) variant of SLC2A4 (P14672)
G39V (p.Gly39Val) in SLC2A4 (P14672) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G39V (p.Gly39Val) variant details
- p.Gly39Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available