TABLE 2.
Reference base |
Variant base |
Genomic position |
Gene region |
Coding/noncoding | Variant frequency (%) |
---|---|---|---|---|---|
G | A | 3724 | NS2A | Yes; M1202I | 1.02 |
G | A | 4463 | NS2B | Yes; D1449N | 1.25 |
A | C | 4505 | NS2B | Yes; I1465L | 2.60a |
G | A | 4517 | NS2B | Yes; A1467T | 2.56a |
C | T | 4520 | NS2B | Yes; L1468F | 1.42 |
A | C | 4551 | NS2B | Yes; H1478P | 1.27 |
G | T | 4808 | NS3 | Yes; A1564S | 1.44 |
T | A | 6818 | NS4A | Yes; S2234T | 3.04a |
G | A | 8801 | NS5 | Yes; E2895K | 1.29 |
The highest percentage is reported for SNV identified in both replicates.