HBV mutation literature information.


  Genetic diversity in enhancer II region of HBV genotype D and its association with advanced liver diseases.
 PMID: 34982798       2022       PloS one
Table: D119N
Discussion: In this study, two mutations were found in the HNF1 Site (K118E/I and D119N) which were more prevalent in HCC (37%) patients as compared to LC (14.2%) and CH (12%).
Discussion: Moreover, double combinational mutation (K118E/I, D119N) within regulatory elements of Enh-II has been shown to affect the replication of HBcAg in situ and can manifest liver disease.



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