T13N (p.Thr13Asn) variant of RAD51D (O75771)
T13N (p.Thr13Asn) 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; Hereditary cancer-predisp. The record also includes structural context.
T13N (p.Thr13Asn) variant details
- p.Thr13Asn
- rs1064795830
- ClinGen CA399092483
- ClinVar RCV001038539
- TOPMed rs1064795830
- Uncertain significance
- Breast-ovarian cancer, familial, susceptibility to, 4; Hereditary cancer-predisp
- Missense
- ClinVar: Uncertain significance (Breast-ovarian cancer, familial, susceptibility to, 4; Hereditar)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available