V35M (p.Val35Met) variant of MEN1 (Menin)
V35M (p.Val35Met) in MEN1 (Menin) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
V35M (p.Val35Met) variant details
- p.Val35Met
- cosmic curated COSV10019
- Ensembl rs2136194077
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available