Run ID: SRR12199400
Sample name:
Date: 03-04-2023 06:37:27
Number of reads: 135450
Percentage reads mapped: 20.01
Strain: lineage4.9;lineage1.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.94 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.32 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.95 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9047 | c.1746C>T | synonymous_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575664 | p.Gly106Ala | missense_variant | 1.0 |
mshA | 576000 | p.Asp218Ala | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776018 | c.2463G>C | synonymous_variant | 0.5 |
mmpL5 | 776021 | c.2460G>C | synonymous_variant | 0.5 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417038 | p.Ser104Cys | missense_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472128 | n.283G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472263 | n.418C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472405 | n.560C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472518 | n.673G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472581 | n.736A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472677 | n.832C>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472678 | n.833T>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472679 | n.834T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472683 | n.839_842delGGGA | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472697 | n.852T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472719 | n.874G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472839 | n.994C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472845 | n.1000G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472874 | n.1029C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472876 | n.1031G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473189 | n.1344C>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473208 | n.1363G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474869 | n.1212G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474902 | n.1245T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475075 | n.1418A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475843 | n.2186G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475853 | n.2196C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476420 | n.2763G>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476433 | n.2776C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476528 | n.2871A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476595 | n.2938C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476602 | n.2945G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476608 | n.2951C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476621 | n.2964C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476628 | n.2971T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476637 | n.2980C>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476645 | n.2988A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476657 | n.3000G>T | non_coding_transcript_exon_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 1.0 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 1.0 |
PPE35 | 2169369 | p.Gly415Ala | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.8 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.8 |
PPE35 | 2170234 | c.378delT | frameshift_variant | 0.5 |
pncA | 2290199 | c.-958C>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.86 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2747294 | p.Gln102Arg | missense_variant | 0.4 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.22 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.33 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4244840 | c.1608G>A | synonymous_variant | 1.0 |
embB | 4247426 | p.Gly305Thr | missense_variant | 0.33 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408341 | c.-139G>T | upstream_gene_variant | 1.0 |