D77G (p.Asp77Gly) variant of MFN2 (Mitofusin-2)
D77G (p.Asp77Gly) in MFN2 (Mitofusin-2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
D77G (p.Asp77Gly) variant details
- p.Asp77Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available