A78D (p.Ala78Asp) variant of DSG1 (Desmoglein-1)
A78D (p.Ala78Asp) in DSG1 (Desmoglein-1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A78D (p.Ala78Asp) variant details
- p.Ala78Asp
- NCI-TCGA Cosmic COSV5713
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available