D17V (p.Asp17Val) variant of MEN1 (Menin)
D17V (p.Asp17Val) in MEN1 (Menin) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
D17V (p.Asp17Val) variant details
- p.Asp17Val
- TOPMed rs1157581823
- gnomAD rs1157581823
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available