G17V (p.Gly17Val) variant of CLDN10 (Claudin-10)
G17V (p.Gly17Val) in CLDN10 (Claudin-10) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G17V (p.Gly17Val) variant details
- p.Gly17Val
- NCI-TCGA Cosmic COSV1001
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available