R79W (p.Arg79Trp) variant of MEF2C (Q06413)
R79W (p.Arg79Trp) in MEF2C (Q06413) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
R79W (p.Arg79Trp) variant details
- p.Arg79Trp
- cosmic curated COSV60928
- Ensembl rs1021588454
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available