Run ID: SRR6045045
Sample name:
Date: 04-04-2023 11:51:55
Number of reads: 347244
Percentage reads mapped: 22.96
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.92 | streptomycin |
embB | 4247652 | p.Ser380Asn | missense_variant | 0.29 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7071 | c.1835delG | frameshift_variant | 0.17 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7634 | c.333C>T | synonymous_variant | 0.29 |
gyrA | 7659 | p.Gly120Ser | missense_variant | 0.22 |
gyrA | 7691 | c.390C>A | synonymous_variant | 0.18 |
gyrA | 9152 | p.Tyr617* | stop_gained | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575693 | p.Pro116Thr | missense_variant | 0.2 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576205 | c.858G>T | synonymous_variant | 0.17 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.5 |
ccsA | 620286 | c.396G>T | synonymous_variant | 0.12 |
ccsA | 620532 | c.642T>G | synonymous_variant | 0.29 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.33 |
rpoB | 761182 | p.Arg459Leu | missense_variant | 0.4 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.12 |
rpoC | 763732 | c.363C>T | synonymous_variant | 0.13 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.2 |
rpoC | 763821 | p.Leu151Pro | missense_variant | 0.15 |
rpoC | 765036 | p.Arg556Leu | missense_variant | 0.2 |
rpoC | 765465 | p.Asp699Val | missense_variant | 0.22 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 767286 | p.Pro1306Gln | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775706 | p.Met925Ile | missense_variant | 0.17 |
mmpL5 | 775834 | p.Ala883Ser | missense_variant | 0.15 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777427 | p.Thr352Pro | missense_variant | 0.4 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781891 | p.Lys111Ile | missense_variant | 0.18 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.2 |
fbiC | 1302852 | c.-79C>T | upstream_gene_variant | 0.14 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.2 |
fbiC | 1303370 | p.Leu147Pro | missense_variant | 0.2 |
fbiC | 1305450 | c.2520C>A | synonymous_variant | 0.25 |
Rv1258c | 1406093 | c.1248A>C | synonymous_variant | 0.25 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471878 | n.33C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1471900 | n.55C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473503 | n.-155G>A | upstream_gene_variant | 0.14 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474016 | n.359C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474022 | n.365G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474044 | n.387C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474045 | n.388C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474053 | n.396G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474275 | n.618T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.29 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834320 | p.Val260Asp | missense_variant | 0.18 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.17 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.17 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.17 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.17 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.29 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.29 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.25 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102122 | c.921C>A | synonymous_variant | 0.33 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154954 | c.1158G>T | synonymous_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168849 | c.1764G>A | synonymous_variant | 0.33 |
PPE35 | 2170595 | p.Leu6Phe | missense_variant | 0.29 |
Rv1979c | 2221755 | c.1410C>A | synonymous_variant | 0.12 |
Rv1979c | 2223266 | c.-102G>T | upstream_gene_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289377 | c.-136A>G | upstream_gene_variant | 0.22 |
kasA | 2519006 | p.Ala298Ser | missense_variant | 1.0 |
ahpC | 2726265 | p.Lys25Gln | missense_variant | 0.25 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.29 |
folC | 2747707 | c.-109C>A | upstream_gene_variant | 0.29 |
pepQ | 2859382 | p.Gly346Val | missense_variant | 0.18 |
Rv2752c | 3065655 | c.537C>T | synonymous_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086997 | p.Thr60Gly | missense_variant | 0.17 |
ald | 3087109 | p.Leu97* | stop_gained | 0.17 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3841115 | c.306T>C | synonymous_variant | 0.25 |
rpoA | 3878115 | p.Lys131Asn | missense_variant | 0.25 |
rpoA | 3878276 | p.Leu78Met | missense_variant | 0.18 |
clpC1 | 4039594 | p.Arg371Gly | missense_variant | 0.29 |
clpC1 | 4039602 | p.Ala368Val | missense_variant | 0.29 |
panD | 4044429 | c.-148C>T | upstream_gene_variant | 0.33 |
embC | 4240139 | p.Gly93Arg | missense_variant | 0.12 |
embC | 4240585 | c.725delG | frameshift_variant | 0.29 |
embC | 4240646 | p.Phe262Val | missense_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242846 | p.Arg995Leu | missense_variant | 0.25 |
embA | 4242856 | c.-377C>A | upstream_gene_variant | 0.22 |
embC | 4243047 | p.Arg1062Gln | missense_variant | 0.29 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4245887 | c.-627T>C | upstream_gene_variant | 0.12 |
embB | 4246416 | c.-98C>A | upstream_gene_variant | 0.17 |
embB | 4248562 | c.2049G>A | synonymous_variant | 0.5 |
aftB | 4267341 | p.Gly499Val | missense_variant | 0.5 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268421 | p.Leu139Pro | missense_variant | 0.17 |
ethR | 4326670 | c.-879G>T | upstream_gene_variant | 0.14 |
ethA | 4326856 | p.Gln206His | missense_variant | 0.4 |
ethA | 4327827 | c.-354A>G | upstream_gene_variant | 0.33 |
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 |
gid | 4408440 | c.-238C>A | upstream_gene_variant | 0.15 |