R32I (p.Arg32Ile) variant of SDHAF2 (Q9NX18)
R32I (p.Arg32Ile) in SDHAF2 (Q9NX18) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
R32I (p.Arg32Ile) variant details
- p.Arg32Ile
- gnomAD rs1277577700
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available