N37D (p.Asn37Asp) variant of BRIP1 (Fanconi anemia group J protein)
N37D (p.Asn37Asp) in BRIP1 (Fanconi anemia group J protein) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
N37D (p.Asn37Asp) variant details
- p.Asn37Asp
- TOPMed rs1256465650
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available