I17M (p.Ile17Met) variant of RAD51D (O75771)
I17M (p.Ile17Met) in RAD51D (O75771) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Breast-ovarian cancer, familial, susceptibility to, 4. The record also includes structural context.
I17M (p.Ile17Met) variant details
- p.Ile17Met
- rs769903986
- ClinGen CA399092403
- ClinVar RCV003643615
- ExAC rs769903986
- Uncertain significance
- Breast-ovarian cancer, familial, susceptibility to, 4
- Missense
- ClinVar: Uncertain significance (Breast-ovarian cancer, familial, susceptibility to, 4)
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available