HPV Mutation Detail Information

> C7732G Search Result


Mutation Information
Mutation Site C7732G
Mutation Type Nucleotide level
Gene/Protein/Region Type LCR
Genotype/Subtype HPV33
Literature Information
PubMed PMID 16960775
Disease High grade squamous intraepithelial lesion; Low grade squamous intraepithelial lesion
Published Year 2006
Journal The Journal of infectious diseases
Title Human papillomavirus type 33 polymorphisms and high-grade squamous intraepithelial lesions of the uterine cervix.
Author Khouadri S,Villa LL,Gagnon S,Koushik A,Richardson H,Ferreira S,Tellier P,Simao J,Matlashewski G,Roger M,Franco EL,Coutlée F
Evidence The C7732G variation, which results in the loss of a putative binding site for the cellular upstream stimulatory factor, was associated with HSILs (age- and site-adjusted OR, 8.0 [95% CI, 1.5-42.8]).

Contents
Description
Mutation Information Note
  • Gene/Protein/Region Type: Virus Gene (e.g. LMP-1) or Virus Protein (e.g. Rep 68) or Virus Region (e.g. S, X)
Literature Information Note
  • Evidence: sentence contains this mutation information in the citation