E96D (p.Glu96Asp) variant of BRAF (P15056)
E96D (p.Glu96Asp) in BRAF (P15056) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes structural context.
E96D (p.Glu96Asp) variant details
- p.Glu96Asp
- ESP rs373545899
- ExAC rs373545899
- TOPMed rs373545899
- gnomAD rs373545899
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available