G138T (p.Gly138Thr) variant of VPS13C (Q709C8)
G138T (p.Gly138Thr) in VPS13C (Q709C8) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G138T (p.Gly138Thr) variant details
- p.Gly138Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available