Run ID: SRR3675557
Sample name:
Date: 04-04-2023 05:33:20
Number of reads: 19266
Percentage reads mapped: 3.63
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472669 | n.824_825insTGGA | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475704 | n.2047C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475752 | n.2095C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475776 | n.2119G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476574 | n.2917A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476594 | n.2937C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476603 | n.2946G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |