HPV Mutation Detail Information

> T7744C Search Result

Mutation Information

Mutation Site	T7744C
Mutation Type	Nucleotide level
Gene/Protein/Region Type	LCR
Genotype/Subtype	HPV52
Country	Canada

Literature Information

PubMed PMID	23015309
Disease	Cervical intraepithelial neoplasia
Published Year	2013
Journal	International journal of cancer
Title	Human papillomavirus type 52 polymorphism and high-grade lesions of the uterine cervix.
Author	Formentin A,Archambault J,Koushik A,Richardson H,Brassard P,Franco EL,Coutlée F
Evidence	CIN2,3 risk was significantly associated with a deletion at nucleotide position 7695 in the LCR (OR 4.9, 95% CI 1.2-20.8), the T7744C variation in the LCR (OR 5.7, 95% CI 1.1-32.0), and the K93R variation in E6 (OR 6.9, 95% CI 1.3-36.8), after adjusting for age, detection of HPV16 or 18 and study site.

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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