A16G (p.Ala16Gly) variant of MSH6 (DNA mismatch repair protein Msh6)
A16G (p.Ala16Gly) in MSH6 (DNA mismatch repair protein Msh6) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
A16G (p.Ala16Gly) variant details
- p.Ala16Gly
- ExAC rs759501511
- TOPMed rs759501511
- gnomAD rs759501511
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available