Run ID: ERR987695
Sample name:
Date: 02-04-2023 13:20:26
Number of reads: 1603249
Percentage reads mapped: 22.81
Strain: lineage4.3.4.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.74 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761180 | c.1374A>G | synonymous_variant | 0.12 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.13 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.13 |
rpoB | 761196 | p.Leu464Val | missense_variant | 0.13 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.14 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.14 |
rpoB | 762101 | c.2295C>T | synonymous_variant | 1.0 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.15 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.14 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.14 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.12 |
rpoC | 764660 | p.Val431Ile | missense_variant | 0.12 |
rpoC | 764665 | c.1296C>T | synonymous_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
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 | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472701 | n.856T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474601 | n.944C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475687 | n.2030C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475688 | n.2031G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475692 | n.2035G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475695 | n.2038G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475699 | n.2042C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475704 | n.2047C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475707 | n.2050T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.44 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155038 | c.1074C>A | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519242 | c.1128C>A | synonymous_variant | 0.15 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4328019 | c.-546G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407980 | p.Pro75Ala | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |