Mutation Information
Mutation Site
|
T1768A |
Mutation Type
|
Nucleotide level |
Gene/Protein/Region Type
|
BCP |
Country
|
China |
Literature Information
PubMed PMID
|
29628773
|
Disease
|
Hepatocellular carcinoma
|
Published Year
|
2018 |
Journal
|
Cancer management and research |
Title
|
The mutation of hepatitis B virus and the prognosis of hepatocellular carcinoma after surgery: a pilot study. |
Author
|
Zhang Y,Huang J,Chen J,Yang K,Chen J,Xu L,Zhou Z,Chen M |
Evidence
|
According to different mutation regions, A1752T/G, T1753C, G1757A, A1762T/G1764A, C1766T, T1768A, A1775G, C1799G, A1846T, T1858C, G1896A, G1898A, G1899A, and Pre S deletion mutations were recognized in 9.8% (39/131), 31.3% (41/131), 42.7% (56/131), 74.0% (97/131), 7.6% (10/131), 5.3% (7/131), 43.5% (57/131), 38.9% (51/131), 35.1% (46/131), 47.3% (62/131), 33.6% (44/131), 17.6% (23/131), 12.2% (16/131), and 16.8% (22/131) cases, respectively (Table 2).
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