Mutation Information
Mutation Site
|
G1899A |
Mutation Type
|
Nucleotide level |
Gene/Protein/Region Type
|
PreC |
Combined Mutation
|
bcp.G1862T+prec.G1899A |
Genotype/Subtype
|
A;D |
Country
|
Eastern India |
Literature Information
PubMed PMID
|
17259736
|
Disease
|
Chronic hepatitis B;
Liver cirrhosis;
Hepatocellular carcinoma
|
Published Year
|
2007 |
Journal
|
Intervirology |
Title
|
G1862T mutation among hepatitis B virus-infected individuals: association with viral genotypes and disease outcome in Kolkata, Eastern India. |
Author
|
Chandra PK,Banerjee A,Datta S,Chakravarty R |
Evidence
|
G1862T mutation is frequently associated with a G1888A and G1899A co-variation. In this study, among the co-variants found, 56% (9/16) of G1862T/A1888 and 100% (2/2) of G1862T/G1888 mutated isolates were quan-tified.
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