HBV Mutation Detail Information

> A1762T Search Result

Mutation Information

Mutation Site	A1762T
Mutation Type	Nucleotide level
Gene/Protein/Region Type	BCP
Combined Mutation	bcp.G1764A+bcp.A1762T;bcp.G1764A+bcp.A1762T+prec.G1896A
Genotype/Subtype	C2
Country	Korea

Literature Information

PubMed PMID	21865669
Disease	Hepatocellular carcinoma
Published Year	2012
Journal	Intervirology
Title	Combination of preS deletions and A1762T/G1764A mutations in HBV subgenotype C2 increases the risk of developing HCC.
Author	Lee MH,Kim DY,Kim JK,Chang HY,Kang SH,Ryu HJ,Ju HL,Kim SU,Lee JM,Park JY,Han KH,Chon CY,Ahn SH
Evidence	Combination of preS deletions and A1762T/G1764A mutations in HBV subgenotype C2 increases the risk of developing HCC.

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