V78F (p.Val78Phe) variant of MFN2 (Mitofusin-2)
V78F (p.Val78Phe) in MFN2 (Mitofusin-2) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
V78F (p.Val78Phe) variant details
- p.Val78Phe
- ExAC rs764695837
- TOPMed rs764695837
- gnomAD rs764695837
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available