I17F (p.Ile17Phe) variant of RAD51D (O75771)
I17F (p.Ile17Phe) in RAD51D (O75771) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
I17F (p.Ile17Phe) variant details
- p.Ile17Phe
- gnomAD rs1002032036
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available