G11V (p.Gly11Val) variant of RAD51D (O75771)
G11V (p.Gly11Val) 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.
G11V (p.Gly11Val) variant details
- p.Gly11Val
- Ensembl rs2091798661
- Uncertain significance
- Breast-ovarian cancer, familial, susceptibility to, 4
- Missense
- ClinVar: Uncertain significance (Breast-ovarian cancer, familial, susceptibility to, 4)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available