Run ID: SRR5007180
Sample name:
Date: 04-04-2023 07:52:02
Number of reads: 295578
Percentage reads mapped: 23.27
Strain:
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490751 | c.-32T>G | upstream_gene_variant | 0.4 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576567 | p.Arg407Gln | missense_variant | 0.33 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.25 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.2 |
rpoB | 759711 | c.-96G>A | upstream_gene_variant | 0.15 |
rpoB | 759921 | p.Arg39Cys | missense_variant | 0.12 |
rpoB | 760814 | c.1008C>T | synonymous_variant | 0.15 |
rpoB | 761483 | c.1677G>T | synonymous_variant | 0.25 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765650 | p.Gln761* | stop_gained | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777009 | p.Pro491Leu | missense_variant | 0.18 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781788 | c.230_232delACT | disruptive_inframe_deletion | 0.12 |
fbiC | 1305435 | c.2505G>A | synonymous_variant | 0.17 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1417371 | c.-24A>G | upstream_gene_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474869 | n.1212G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476214 | n.2557G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918399 | p.Asp154Tyr | missense_variant | 0.29 |
tlyA | 1918513 | p.Val192Ile | missense_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169178 | p.Ala479Thr | missense_variant | 0.2 |
PPE35 | 2170312 | p.Arg101Trp | missense_variant | 0.4 |
Rv1979c | 2222069 | p.Ala366Thr | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518147 | c.33C>T | synonymous_variant | 0.3 |
kasA | 2518161 | p.Val16Gly | missense_variant | 0.25 |
pepQ | 2860367 | p.Gly18Arg | missense_variant | 0.2 |
ald | 3086747 | c.-73A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087483 | p.Ala222Pro | missense_variant | 0.17 |
fprA | 3473853 | c.-154C>T | upstream_gene_variant | 0.22 |
fprA | 3473928 | c.-79T>C | upstream_gene_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568547 | c.131_132dupTG | frameshift_variant | 0.18 |
Rv3236c | 3613142 | c.-26A>G | upstream_gene_variant | 0.33 |
Rv3236c | 3613167 | c.-51C>A | upstream_gene_variant | 0.4 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.33 |
clpC1 | 4040162 | c.543G>A | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4246509 | c.-5C>T | upstream_gene_variant | 0.5 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269864 | c.-31C>G | upstream_gene_variant | 0.5 |
ethR | 4327105 | c.-444G>A | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |