A59G (p.Ala59Gly) variant of VPS13C (Q709C8)
A59G (p.Ala59Gly) 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.
A59G (p.Ala59Gly) variant details
- p.Ala59Gly
- NCI-TCGA Cosmic COSV5116
- cosmic curated COSV51163
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available