HBV Mutation Detail Information

> C1817T Search Result

Mutation Information

Mutation Site	C1817T
Mutation Type	Nucleotide level
Gene/Protein/Region Type	PreC
Country	Argentina

Literature Information

PubMed PMID	25822666
Disease	Acute exacerbation of chronic hepatitis B
Published Year	2015
Journal	PloS one
Title	Hepatitis B virus genotype distribution and genotype-specific BCP/preCore substitutions in acute and chronic infections in Argentina.
Author	González López Ledesma MM,Mojsiejczuk LN,Rodrigo B,Sevic I,Mammana L,Galdame O,Gadano A,Fainboim H,Campos R,Flichman D
Evidence	In the preCore region, G1896A was the most common mutation (55.2%), whereas other mutations that prevent HBeAg synthesis, such as those affecting the preCore initiation codon (nt 1814–1816), mutations (C1817T, G1897A), insertions and deletions that create a premature stop codon, were observed in a lower frequency (33.3%).

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