V3G (p.Val3Gly) variant of SDHAF2 (Q9NX18)
V3G (p.Val3Gly) in SDHAF2 (Q9NX18) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
V3G (p.Val3Gly) variant details
- p.Val3Gly
- ExAC rs760006057
- gnomAD rs760006057
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available