W41C (p.Trp41Cys) variant of NF2 (Merlin)
W41C (p.Trp41Cys) in NF2 (Merlin) 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.
W41C (p.Trp41Cys) variant details
- p.Trp41Cys
- Ensembl rs2146851659
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available