N8D (p.Asn8Asp) variant of CDKN1B (P46527)
N8D (p.Asn8Asp) in CDKN1B (P46527) 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.
N8D (p.Asn8Asp) variant details
- p.Asn8Asp
- TOPMed rs1946485763
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available