V50D (p.Val50Asp) variant of MEN1 (Menin)
V50D (p.Val50Asp) in MEN1 (Menin) 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.
V50D (p.Val50Asp) variant details
- p.Val50Asp
- Ensembl rs2136192240
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available