Mutation Information
Mutation Site
|
A1652G |
Mutation Type
|
Nucleotide level |
Gene/Protein/Region Type
|
EnhII |
Country
|
China |
Literature Information
PubMed PMID
|
20959817
|
Disease
|
Chronic hepatitis B;
Liver cirrhosis;
Hepatocellular carcinoma
|
Published Year
|
2011 |
Journal
|
The American journal of gastroenterology |
Title
|
Association between the various mutations in viral core promoter region to different stages of hepatitis B, ranging of asymptomatic carrier state to hepatocellular carcinoma. |
Author
|
Yin J,Xie J,Liu S,Zhang H,Han L,Lu W,Shen Q,Xu G,Dong H,Shen J,Zhang J,Han J,Wang L,Liu Y,Wang F,Zhao J,Zhang Q,Ni W,Wang H,Cao G |
Evidence
|
C1653T, T1674C, G1719T, A1762T, and A1846T were significantly associated with HCC, whereas A1652G, C1673T, A1726C,A1727T, C1730G, T1768A, C1773T, and C1799G were inverselyassociated with HCC, as compared with the patients with LC in the genotype C HBV-infected patients seronegative for HBeAg.
|
|
|