R86T (p.Arg86Thr) variant of MFN2 (Mitofusin-2)
R86T (p.Arg86Thr) in MFN2 (Mitofusin-2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R86T (p.Arg86Thr) variant details
- p.Arg86Thr
- NCI-TCGA Cosmic COSV5242
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available