Run ID: ERR2229554
Sample name:
Date: 31-03-2023 17:18:31
Number of reads: 810726
Percentage reads mapped: 86.92
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.26 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6510 | p.Arg424Leu | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491746 | p.Glu322Gln | missense_variant | 0.22 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.22 |
mshA | 576628 | c.1281G>A | synonymous_variant | 0.18 |
rpoB | 760898 | c.1092C>T | synonymous_variant | 0.17 |
rpoB | 761499 | p.Val565Met | missense_variant | 0.14 |
rpoB | 761509 | p.Ser568Tyr | missense_variant | 0.12 |
rpoC | 764609 | p.Arg414Trp | missense_variant | 0.17 |
rpoC | 764849 | p.His494Asn | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777084 | p.Asn466Thr | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303261 | p.Pro111Thr | missense_variant | 0.2 |
fbiC | 1303560 | c.630G>T | synonymous_variant | 0.12 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304491 | c.1561_1562insGT | frameshift_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474236 | n.579G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474255 | n.598C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474903 | n.1246T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475163 | n.1506T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475507 | n.1850C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475550 | n.1893A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475552 | n.1895G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475574 | n.1917C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476640 | n.2983C>A | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.32 |
fabG1 | 1673558 | p.His40Pro | missense_variant | 0.2 |
fabG1 | 1674127 | p.Ser230Gly | missense_variant | 0.2 |
inhA | 1674162 | c.-40C>A | upstream_gene_variant | 0.33 |
inhA | 1674504 | c.303C>G | synonymous_variant | 0.2 |
rpsA | 1834676 | p.Gly379Cys | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102146 | c.897G>T | synonymous_variant | 0.29 |
ndh | 2103097 | c.-55C>T | upstream_gene_variant | 0.13 |
katG | 2155117 | p.Phe332Tyr | missense_variant | 0.14 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.12 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.12 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.22 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.22 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.31 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.36 |
Rv1979c | 2222833 | p.Ser111Tyr | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289808 | c.-567C>A | upstream_gene_variant | 0.18 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.33 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.33 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.14 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.21 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.21 |
folC | 2746585 | c.1014G>T | synonymous_variant | 0.14 |
folC | 2747485 | p.Trp38Cys | missense_variant | 0.22 |
ribD | 2986892 | p.Ser18Arg | missense_variant | 0.12 |
Rv2752c | 3065757 | c.435C>G | synonymous_variant | 0.15 |
thyA | 3074190 | c.282C>T | synonymous_variant | 0.14 |
ald | 3087748 | p.Thr310Asn | missense_variant | 0.22 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.5 |
fprA | 3474808 | p.Val268Met | missense_variant | 0.5 |
fprA | 3474977 | p.Tyr324Cys | missense_variant | 0.33 |
fbiA | 3640394 | c.-149G>T | upstream_gene_variant | 0.17 |
fbiA | 3641484 | p.Asn314Lys | missense_variant | 0.2 |
fbiB | 3642842 | c.1308C>T | synonymous_variant | 0.18 |
alr | 3840503 | c.918T>C | synonymous_variant | 0.13 |
rpoA | 3878344 | p.Arg55Pro | missense_variant | 0.15 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.12 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.15 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.18 |
clpC1 | 4039031 | c.1674T>C | synonymous_variant | 0.2 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.13 |
embC | 4240655 | p.Ala265Thr | missense_variant | 0.15 |
embC | 4242558 | p.Gln899Arg | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243896 | p.Ala222Thr | missense_variant | 0.13 |
embB | 4246544 | p.Thr11Pro | missense_variant | 1.0 |
embB | 4247498 | p.Pro329Thr | missense_variant | 0.18 |
embB | 4247559 | p.Trp349Leu | missense_variant | 0.13 |
aftB | 4268389 | c.447delG | frameshift_variant | 0.2 |
ethA | 4326643 | p.Asp277Glu | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |