P32R (p.Pro32Arg) variant of MEN1 (Menin)
P32R (p.Pro32Arg) in MEN1 (Menin) is a missense change. Clinical records from ClinVar and UniProt describe it as pathogenic/likely pathogenic in the context of Hereditary cancer-predisposing syndrome; Multiple endocrine neoplasia, type 1. The record also includes structural context.
P32R (p.Pro32Arg) variant details
- p.Pro32Arg
- cosmic curated COSV56340
- Pathogenic/Likely pathogenic
- Hereditary cancer-predisposing syndrome; Multiple endocrine neoplasia, type 1
- Missense
- ClinVar: Pathogenic/Likely pathogenic (Hereditary cancer-predisposing syndrome; Multiple endocrine neop)
- UniProt: Likely pathogenic
- Structural context available