A67G (p.Ala67Gly) variant of KMT2D (O14686)
A67G (p.Ala67Gly) in KMT2D (O14686) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
A67G (p.Ala67Gly) variant details
- p.Ala67Gly
- ExAC rs763380529
- gnomAD rs763380529
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available