Run ID: ERR2514137
Sample name:
Date: 31-03-2023 20:08:25
Number of reads: 602483
Percentage reads mapped: 88.35
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 760314 | p.Val170Phe | missense_variant | 1.0 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.48 | streptomycin |
katG | 2155129 | p.Trp328Leu | missense_variant | 1.0 | isoniazid |
pncA | 2288933 | p.Tyr103* | stop_gained | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 7199 | p.Glu654Lys | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9818 | c.2517A>G | splice_region_variant&stop_retained_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575972 | p.Glu209Lys | missense_variant | 0.12 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760309 | p.Val168Ala | missense_variant | 1.0 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.12 |
rpoB | 761058 | p.Val418Thr | missense_variant | 0.12 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.12 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.12 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.1 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.15 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.12 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.11 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.11 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.1 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.11 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.12 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.12 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.11 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.11 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.12 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.11 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.1 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.1 |
rpoC | 764703 | p.Lys445Ser | missense_variant | 0.1 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.11 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.12 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775689 | c.2791delG | frameshift_variant | 0.17 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 778588 | p.Gln106His | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.94 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472114 | n.269A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472151 | n.306C>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472188 | n.343A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472207 | n.362A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472208 | n.363A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472244 | n.399C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472274 | n.429A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472687 | n.842A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472975 | n.1130T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472988 | n.1143T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473001 | n.1156G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473017 | n.1172A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473047 | n.1202C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473109 | n.1264T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473291 | n.1446G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475692 | n.2035G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475695 | n.2038G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475704 | n.2047C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475759 | n.2102C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476458 | n.2801T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673402 | c.-38A>G | upstream_gene_variant | 0.1 |
inhA | 1674833 | p.Ala211Val | missense_variant | 0.22 |
rpsA | 1833364 | c.-178C>A | upstream_gene_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155122 | c.990C>T | synonymous_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169079 | c.1533dupG | frameshift_variant | 0.12 |
PPE35 | 2169706 | p.Gly303Arg | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518598 | p.Ala162Thr | missense_variant | 0.12 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.12 |
kasA | 2518609 | p.Met165Ile | missense_variant | 0.12 |
kasA | 2518889 | p.Ala259Thr | missense_variant | 0.11 |
kasA | 2518947 | p.Val278Ala | missense_variant | 0.11 |
eis | 2714569 | p.Ala255Gly | missense_variant | 0.25 |
folC | 2746800 | p.Arg267Trp | missense_variant | 0.14 |
folC | 2747158 | c.441G>C | synonymous_variant | 0.11 |
pepQ | 2860251 | c.168C>T | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449096 | p.Gly198Asp | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3612831 | p.Asp96Asn | missense_variant | 0.17 |
Rv3236c | 3613279 | c.-163C>T | upstream_gene_variant | 0.11 |
rpoA | 3877991 | p.Lys173Glu | missense_variant | 0.11 |
ddn | 3986705 | c.-138delA | upstream_gene_variant | 0.14 |
clpC1 | 4039067 | c.1638G>A | synonymous_variant | 0.15 |
clpC1 | 4039455 | p.Ala417Val | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4249330 | p.Met939Ile | missense_variant | 0.23 |
aftB | 4267499 | c.1337delC | frameshift_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268354 | c.483G>A | synonymous_variant | 0.17 |
aftB | 4268518 | p.Ala107Thr | missense_variant | 0.11 |
ubiA | 4269322 | p.Pro171Leu | missense_variant | 0.15 |
ubiA | 4269859 | c.-26A>C | upstream_gene_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407640 | p.Val188Glu | missense_variant | 0.12 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |