HBV Mutation Detail Information

> A1814T Search Result

Mutation Information

Mutation Site	A1814T
Mutation Type	Nucleotide level
Gene/Protein/Region Type	PreC
Country	Sudan

Literature Information

PubMed PMID	23865777
Disease	HBV associated liver disease
Published Year	2013
Journal	BMC infectious diseases
Title	Molecular characterization of hepatitis B virus in liver disease patients and asymptomatic carriers of the virus in Sudan.
Author	Yousif M,Mudawi H,Bakhiet S,Glebe D,Kramvis A
Evidence	In 22/49 HBeAg-negative sera, the absence of HBeAg was as a result of missense mutations affecting the translation of the HBeAg precursor: 18 had the classical stop codon mutation G1896A (p< 0.05, when comparing isolates from HBeAg-negative and -positive sera) and 4 had initiation codon mutations, 2 A1814T and 2 T1815C.

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