HBV Mutation Detail Information

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Mutation Information
Mutation Site V17F
Mutation Type Amino acid level
Gene/Protein/Region Type PreC
Combined Mutation bcp.G1764A+bcp.A1762T+prec.G1862T
Amino acid_Mutation G1862T
Genotype/Subtype A
Viral Reference AF160501; X75663; X75657; X72702; X01587; D00331; X70185
Country India
Literature Information
PubMed PMID 16789012
Disease Chronic hepatitis B
Published Year 2006
Journal Journal of medical virology
Title Basal core promoter, precore region mutations of HBV and their association with e antigen, genotype, and severity of liver disease in patients with chronic hepatitis B in India.
Author Chauhan R,Kazim SN,Bhattacharjee J,Sakhuja P,Sarin SK
Evidence 17 (37%) of 46 HBeAg-positive patients had G1862T (V17F) compared to 4 (11%) of 36 HBeAg-negative patients (P < 0.05) (Table II).

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