TABLE 1.
Mutation position | Variant name | Gene position | Mutation type | Codon position | No. of isolates | No. of sublineages |
---|---|---|---|---|---|---|
776210 | mmpL5 C2271A | 2271 | N | Y757* | 2 | 2 |
777499 | mmpL5 C982T | 982 | N | R328* | 2 | 2 |
777581 | mmpL5 C900A | 900 | N | Y300* | 293 | 2 |
778086 | mmpL5 395insC | 395 | Ins | 132 | 6 | 2 |
779127 | mmpR 138insG | 138 | Ins | 46 | 5 | 4 |
779181 | mmpR 192-198delG | 192 | Del | 64 | 20 | 4 |
779181 | mmpR 192-198insG | 192 | Ins | 64 | 86 | 2 |
779407 | mmpR 418insG | 418 | Ins | 140 | 6 | 1 |
2714753 | eis C580T | 580 | N | Q194* | 10 | 2 |
2715287 | eis 46insC | 46 | Ins | 16 | 3 | 2 |
2715305 | eis G28T | 28 | N | E10* | 6 | 2 |
2715330 | eis G3A | 3 | S | V1V | 6 | 2 |
2715342 | eis G-10A | −10 eis | I | 293 | 18 | |
2715344 | eis C-12T | −12 eis | I | 332 | 17 | |
2715346 | eis C-14T | −14 eis | I | 181 | 19 | |
2715369 | eis G-37T | −37 eis | I | 285 | 8 | |
2726105 | ahpC G-88A | −88 ahpC | I | 3,350 | 12 | |
2726141 | ahpC C-52A | −52 ahpC | I | 91 | 10 | |
2726141 | ahpC C-52T | −52 ahpC | I | 92 | 25 | |
2726145 | ahpC G-48A | −48 ahpC | I | 85 | 20 | |
3568487 | whiB7 193insG | 193 | Ins | 65 | 3 | 3 |
3568488 | whiB7 192delC | 192 | Del | 64 | 573 | 3 |
3568547 | whiB7 133delCA | 133 | Del | 45 | 2 | 2 |
3568626 | whiB7 54delA | 54 | Del | 18 | 61 | 2 |
3568779 | whiB7 T-100C | −100 whiB7 | I | 256 | 2 | |
3568857 | whiB7 C-178T | −178 whiB7 | I | 73 | 2 | |
3568921 | whiB7 G-242C | −242 whiB7 | I | 117 | 2 | |
3569029 | whiB7 A-350G | −350 whiB7 | I | 249 | 3 |
Mutations that occur in our sample of 31,440 clinical isolates within the mmpL5, mmpS5, mmpR, ahpC, eis, and whiB7 coding sequences and the oxyR-ahpC, eis-Rv2417c, whiB7-uvrD2 intergenic regions are shown (Fig. 1). Mutations in regulator regions (mmpR, oxyR-ahpC, eis-Rv2417c, and whiB7-uvrD2) reported in this table were among the four most commonly detected variants in each region. Mutations in regulated regions (mmpL5, mmpS5, ahpC, eis, and whiB7) reported in this table were present in at least two MTBC sublineages. The full set of mutations detected within these genomic regions is reported in Table S1 in the supplemental material. S, synonymous; N, nonsynonymous; I, intergenic.