HBV Mutation Detail Information

> P79Q Search Result

Mutation Information

Mutation Site	P79Q
Mutation Type	Amino acid level
Gene/Protein/Region Type	C
Genotype/Subtype	C
Country	Japan

Literature Information

PubMed PMID	27998820
Disease	Chronic hepatitis B
Published Year	2017
Journal	Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
Title	Core I97L mutation in conjunction with P79Q is associated with persistent low HBV DNA and HBs antigen clearance in patients with chronic hepatitis B.
Author	Honda T,Ishigami M,Ishizu Y,Kuzuya T,Hayashi K,Ishikawa T,Murakami Y,Iwadate M,Umeyama H,Toyoda H,Kumada T,Katano Y,Goto H,Hirooka Y
Evidence	Core I97L mutation in conjunction with P79Q is associated with persistent low HBV DNA and HBs antigen clearance in patients withChronic hepatitis B.

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