L39M (p.Leu39Met) variant of MEN1 (Menin)
L39M (p.Leu39Met) in MEN1 (Menin) is a missense change. Clinical records from EBI and UniProt describe it as likely benign in the context of in MEN1. The record also includes structural context.
L39M (p.Leu39Met) variant details
- p.Leu39Met
- TOPMed rs863224438
- gnomAD rs863224438
- Likely benign
- in MEN1
- Missense
- EBI: Likely benign (in MEN1)
- UniProt: Likely benign (in MEN1)
- Structural context available