F31V (p.Phe31Val) variant of SDHAF2 (Q9NX18)
F31V (p.Phe31Val) in SDHAF2 (Q9NX18) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
F31V (p.Phe31Val) variant details
- p.Phe31Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available