V7F (p.Val7Phe) variant of CHEK2 (O96017)
V7F (p.Val7Phe) in CHEK2 (O96017) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
V7F (p.Val7Phe) variant details
- p.Val7Phe
- cosmic curated COSV10884
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available