K26N (p.Lys26Asn) variant of RAD51D (O75771)
K26N (p.Lys26Asn) 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.
K26N (p.Lys26Asn) variant details
- p.Lys26Asn
- rs2142480132
- Ensembl rs2142480132
- ClinGen CA399092264
- ClinVar RCV002801444
- 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