Result: Amino acid transitions induced by
G1719T,
A1726C,
A1752G/T and
BCP A1762T/
G1764A mutants had higher prevalence of 39.7% (23/58), 29.3% (17/58), 27.6% (16/58) and 31.0% (18/58), which mainly occurred in genotype C (21/23), genotype B (16/17), genotype B (13/16) and genotype C (16/18) infection patients, respectively.
Result: In addition, among the twelve hotspots,
G1719T and
T1753V were significantly associated with genotype C (P < 0.05), while
A1726C and
A1752G/T were genotype B related (P < 0.05) (Table 2).