| Mutation |
Total (n=207) |
HCC (n=102) |
CH (n=105) |
P value |
OR (95% CI) |
| T1653 |
27 (13.0%) |
18 (17.6%) |
9 (8.5%) |
0.088 |
|
| V1753 |
43 (29.5%) |
43 (42.1%)* |
18 (17.1%) |
0.034 |
3.071 (1.68–5.86) |
| T1762/A1764 |
120 (57.9%) |
66 (64.7%) |
54 (51.4%) |
0.802 |
|
| T1766 |
26 (25.5%) |
19 (18.6%)* |
7 (6.7%) |
0.044 |
2.146 (0.96–7.12) |
| A1768 |
35 (16.9%) |
26 (24.5%)* |
9 (8.6%) |
0.021 |
2.869 (1.21–6.49) |
HCC: Hepatocellular Carcinoma; CH: Chronic Heptitis; OR: Odds Ratio; CI: Confidence Interval
*P<0.05 comparing the frequency of CP mutation in HCC vs.CH. |
