A novel TP53 splicing mutation in a Li-Fraumeni syndrome family: a patient with Wilms' tumour is not a mutation carrier

Br J Cancer. 1998 Oct;78(8):1081-3. doi: 10.1038/bjc.1998.631.

Abstract

We report a Li-Fraumeni syndrome family in which we have detected a splice acceptor mutation in intron 3 of TP53. The mutation affects one of the invariant residues at the splice acceptor site, as a result of which two aberrant transcripts are produced. A child with Wilms' tumour aged 3 years in this family was shown not to be a mutation carrier.

Publication types

  • Case Reports

MeSH terms

  • Child, Preschool
  • Exons
  • Female
  • Germ-Line Mutation
  • Heterozygote
  • Humans
  • Kidney Neoplasms / genetics*
  • Li-Fraumeni Syndrome / genetics*
  • Male
  • Pedigree
  • Point Mutation*
  • Tumor Suppressor Protein p53 / genetics*
  • Wilms Tumor / genetics*

Substances

  • Tumor Suppressor Protein p53