V9M (p.Val9Met) variant of MAX (Protein max)
V9M (p.Val9Met) in MAX (Protein max) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
V9M (p.Val9Met) variant details
- p.Val9Met
- NCI-TCGA Cosmic COSV5241
- cosmic curated COSV52419
- ExAC rs201743423
- TOPMed rs201743423
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance (in PCC)
- UniProt: Uncertain significance (in PCC)
- Structural context available