M1V (p.Met1Val) variant of MEN1 (Menin)
M1V (p.Met1Val) in MEN1 (Menin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic/likely pathogenic in the context of not specified; Hereditary cancer-predisposing syndrome; Multiple endocrine neopl. The available variant effect predictions contribute to a CATVariant prioritization score of 0.92 / 1. The record also includes published literature and structural context.
M1V (p.Met1Val) variant details
- p.Met1Val
- rs386134250
- ClinGen CA009318
- ClinVar RCV000030198
- ClinVar RCV000480514
- Pathogenic/Likely pathogenic
- not specified; Hereditary cancer-predisposing syndrome; Multiple endocrine neopl
- Missense
- Variant Prioritization Score for Impact Estimate 0.921
- MetaLR 0.97
- MetaSVM 1.09
- PolyPhen-2 0.65
- SIFT 0.02
- MutPred 0.73
- ClinVar: Pathogenic/Likely pathogenic (not specified; Hereditary cancer-predisposing syndrome; Multiple)
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)
- Cited in: Guidelines for diagnosis and therapy of MEN type 1 and type 2. (PMID 11739416)