Abstract: A total of 10 mutations (including
pre-S2 start codon mutation and
pre-S deletion in
pre-S gene,
G1613A,
C1653T,
A1762T, and
G1764A mutations in
X gene,
A2159G,
A2189Y,
G2203W, and
C2288R mutations in
C gene) showed an increased risk of
HCC.