Run ID: ERR4872193
Sample name:
Date: 01-04-2023 21:26:51
Number of reads: 6245183
Percentage reads mapped: 86.15
Strain: lineage4.6
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Asp | missense_variant | 1.0 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.82 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8266 | p.Ala322Glu | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.23 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472108 | n.263C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472129 | n.284G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472135 | n.290C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472207 | n.362A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472545 | n.700A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472572 | n.727T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472659 | n.814G>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472697 | n.852T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472715 | n.870C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472719 | n.874G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474208 | n.551C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474213 | n.556G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474263 | n.606G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476353 | n.2696G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476427 | n.2770G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476528 | n.2871A>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476582 | n.2925T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.16 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.38 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |