|
Mutation Information
|
Mutation Site
|
G1896A |
|
Mutation Type
|
Nucleotide level |
|
Gene/Protein/Region Type
|
PreC |
|
Combined Mutation
|
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
|
The prevalence of preS deletions and G1896A and A1762T/G1764A mutations was evaluated.
|
|
|
HBV Mutation Detail Information