L26V (p.Leu26Val) variant of SDHAF2 (Q9NX18)
L26V (p.Leu26Val) in SDHAF2 (Q9NX18) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
L26V (p.Leu26Val) variant details
- p.Leu26Val
- ExAC rs751530375
- gnomAD rs751530375
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available