Run ID: ERR5865353
Sample name:
Date: 01-04-2023 23:58:01
Number of reads: 469319
Percentage reads mapped: 99.57
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 | 7582 | p.Asp94Ala | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289252 | c.-11A>G | upstream_gene_variant | 1.0 | pyrazinamide |
eis | 2715342 | c.-10G>A | upstream_gene_variant | 1.0 | kanamycin |
embB | 4247429 | p.Met306Leu | missense_variant | 1.0 | ethambutol |
ethA | 4326770 | c.703delT | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5471 | p.Ala78Ser | missense_variant | 0.2 |
gyrB | 5721 | p.Gly161Val | missense_variant | 0.2 |
gyrA | 7000 | c.-302C>G | upstream_gene_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7420 | p.Ala40Glu | missense_variant | 0.15 |
gyrA | 7425 | p.Pro42Ser | missense_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7736 | c.435C>A | synonymous_variant | 0.43 |
gyrA | 7739 | p.Asp146Glu | missense_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9464 | c.2163C>A | synonymous_variant | 0.25 |
fgd1 | 491536 | c.754C>T | synonymous_variant | 0.5 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576056 | p.Val237Met | missense_variant | 0.17 |
mshA | 576557 | p.His404Asn | missense_variant | 0.2 |
mshA | 576577 | c.1230C>A | synonymous_variant | 0.2 |
ccsA | 619750 | c.-141C>A | upstream_gene_variant | 0.22 |
ccsA | 619893 | c.3G>T | start_lost | 0.29 |
ccsA | 619992 | p.Phe34Leu | missense_variant | 0.25 |
ccsA | 620503 | p.Glu205* | stop_gained | 0.22 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759652 | c.-155G>T | upstream_gene_variant | 0.21 |
rpoB | 759772 | c.-35C>A | upstream_gene_variant | 0.17 |
rpoB | 759960 | p.Thr52Ala | missense_variant | 0.12 |
rpoB | 760178 | c.372G>T | synonymous_variant | 0.17 |
rpoB | 760254 | p.Asp150Tyr | missense_variant | 0.2 |
rpoB | 760628 | p.Lys274Asn | missense_variant | 0.17 |
rpoB | 761066 | c.1260G>T | synonymous_variant | 0.18 |
rpoB | 761351 | c.1545C>T | synonymous_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764224 | p.Lys285Asn | missense_variant | 0.15 |
rpoC | 764579 | p.Asp404Tyr | missense_variant | 0.23 |
rpoC | 764728 | c.1361dupC | frameshift_variant | 0.11 |
rpoC | 765461 | p.Asn698His | missense_variant | 1.0 |
rpoC | 765750 | p.Pro794His | missense_variant | 0.2 |
rpoC | 766202 | p.Gly945Cys | missense_variant | 0.25 |
rpoC | 766346 | p.Glu993* | stop_gained | 0.18 |
rpoC | 766393 | c.3024C>A | synonymous_variant | 0.17 |
rpoC | 766411 | c.3042C>A | synonymous_variant | 0.18 |
rpoC | 766414 | p.Phe1015Leu | missense_variant | 0.2 |
rpoC | 766475 | p.Glu1036* | stop_gained | 0.25 |
rpoC | 766489 | c.3120G>A | synonymous_variant | 0.25 |
rpoC | 766874 | p.Asp1169Tyr | missense_variant | 0.2 |
rpoC | 767088 | p.Cys1240Phe | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775709 | p.Phe924Leu | missense_variant | 0.25 |
mmpL5 | 776025 | p.Ser819* | stop_gained | 0.25 |
mmpL5 | 776082 | p.Ala800Val | missense_variant | 0.17 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776235 | p.Thr749Lys | missense_variant | 0.2 |
mmpL5 | 776270 | p.Lys737Asn | missense_variant | 0.2 |
mmpL5 | 776458 | p.Ala675Ser | missense_variant | 0.2 |
mmpL5 | 776477 | c.2004G>T | synonymous_variant | 0.2 |
mmpL5 | 776528 | p.Gln651His | missense_variant | 0.18 |
mmpL5 | 776945 | p.Glu512Asp | missense_variant | 0.2 |
mmpL5 | 776981 | c.1500G>T | synonymous_variant | 0.18 |
mmpL5 | 777004 | p.Glu493* | stop_gained | 0.22 |
mmpL5 | 777152 | p.Met443Ile | missense_variant | 0.25 |
mmpL5 | 777155 | c.1326G>T | synonymous_variant | 0.22 |
mmpL5 | 777406 | p.Ala359Ser | missense_variant | 0.18 |
mmpL5 | 778939 | c.-459C>A | upstream_gene_variant | 0.29 |
mmpL5 | 778957 | c.-477C>A | upstream_gene_variant | 0.25 |
mmpL5 | 779400 | c.-920C>A | upstream_gene_variant | 0.17 |
mmpS5 | 779489 | c.-584C>A | upstream_gene_variant | 0.2 |
mmpS5 | 779498 | c.-593G>T | upstream_gene_variant | 0.22 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781379 | c.-181G>T | upstream_gene_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781446 | c.-114G>T | upstream_gene_variant | 0.2 |
rpsL | 781449 | c.-111G>T | upstream_gene_variant | 0.2 |
rpsL | 781451 | c.-109G>T | upstream_gene_variant | 0.18 |
rpsL | 781590 | p.Gly11Cys | missense_variant | 0.29 |
rpsL | 781692 | p.Pro45Thr | missense_variant | 0.14 |
rplC | 801308 | p.Ala167Asp | missense_variant | 0.17 |
fbiC | 1303371 | c.441C>A | synonymous_variant | 0.29 |
fbiC | 1304197 | p.Gly423Cys | missense_variant | 0.18 |
fbiC | 1304286 | c.1356G>T | synonymous_variant | 0.2 |
fbiC | 1304374 | p.Glu482* | stop_gained | 0.25 |
fbiC | 1304831 | p.Ser634Tyr | missense_variant | 0.2 |
fbiC | 1304881 | p.Glu651* | stop_gained | 0.2 |
Rv1258c | 1406404 | p.Val313Phe | missense_variant | 0.14 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406891 | c.450C>T | synonymous_variant | 0.18 |
Rv1258c | 1407216 | p.Gly42Val | missense_variant | 0.15 |
embR | 1416494 | p.Gly285Val | missense_variant | 0.15 |
embR | 1416672 | p.Gly226Arg | missense_variant | 0.22 |
embR | 1416795 | p.Gly185Trp | missense_variant | 0.22 |
atpE | 1461020 | c.-25C>A | upstream_gene_variant | 0.17 |
atpE | 1461029 | c.-16C>A | upstream_gene_variant | 0.18 |
atpE | 1461051 | p.Pro3Thr | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473933 | n.276C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474702 | n.1045G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474785 | n.1128T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475316 | n.1659G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476304 | n.2647G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476569 | n.2912G>T | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673271 | c.-169G>T | upstream_gene_variant | 0.18 |
fabG1 | 1673647 | p.Arg70Cys | missense_variant | 0.22 |
fabG1 | 1673668 | p.Glu77* | stop_gained | 0.18 |
inhA | 1674414 | c.213G>A | synonymous_variant | 0.2 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917823 | c.-117C>T | upstream_gene_variant | 0.15 |
tlyA | 1917851 | c.-89C>A | upstream_gene_variant | 0.18 |
tlyA | 1917921 | c.-19G>T | upstream_gene_variant | 0.25 |
tlyA | 1917939 | c.-1C>A | upstream_gene_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918540 | p.Pro201Thr | missense_variant | 0.18 |
ndh | 2102417 | p.Ala209Val | missense_variant | 1.0 |
katG | 2154279 | c.1833C>A | synonymous_variant | 0.25 |
katG | 2154610 | p.Pro501Gln | missense_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154975 | p.Ala379Ser | missense_variant | 0.18 |
katG | 2155448 | p.Ala222Ser | missense_variant | 0.25 |
katG | 2156570 | c.-459C>A | upstream_gene_variant | 0.17 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168213 | c.2400G>T | synonymous_variant | 0.29 |
PPE35 | 2168276 | c.2337C>A | synonymous_variant | 0.18 |
PPE35 | 2168491 | p.Ala708Ser | missense_variant | 0.17 |
PPE35 | 2168526 | p.Gly696Val | missense_variant | 0.2 |
PPE35 | 2169233 | p.Leu460Phe | missense_variant | 0.21 |
PPE35 | 2170363 | p.Glu84* | stop_gained | 0.23 |
PPE35 | 2170445 | c.168G>T | synonymous_variant | 0.17 |
PPE35 | 2170623 | c.-11G>T | upstream_gene_variant | 0.15 |
PPE35 | 2170673 | c.-61C>A | upstream_gene_variant | 0.25 |
Rv1979c | 2222167 | p.Ser333Ile | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223336 | c.-172G>T | upstream_gene_variant | 0.3 |
pncA | 2289635 | c.-394G>T | upstream_gene_variant | 0.17 |
kasA | 2518301 | p.His63Asn | missense_variant | 0.22 |
kasA | 2518580 | p.Leu156Met | missense_variant | 0.18 |
kasA | 2518750 | p.Met212Ile | missense_variant | 0.33 |
kasA | 2518778 | p.Glu222* | stop_gained | 0.22 |
kasA | 2518817 | p.Asp235Tyr | missense_variant | 0.2 |
kasA | 2519076 | p.Ala321Glu | missense_variant | 0.25 |
kasA | 2519151 | p.Ser346* | stop_gained | 0.22 |
eis | 2714167 | p.Ala389Val | missense_variant | 0.15 |
eis | 2714349 | c.984G>T | synonymous_variant | 0.33 |
eis | 2714942 | p.Tyr131His | missense_variant | 0.12 |
eis | 2715126 | p.Leu69Phe | missense_variant | 0.25 |
eis | 2715156 | c.177C>A | synonymous_variant | 0.4 |
eis | 2715395 | c.-63C>T | upstream_gene_variant | 0.22 |
folC | 2746272 | p.Ala443Ser | missense_variant | 0.25 |
folC | 2746312 | c.1287G>T | synonymous_variant | 0.17 |
folC | 2746683 | p.Leu306Ile | missense_variant | 0.18 |
folC | 2746835 | p.Ser255* | stop_gained | 0.22 |
folC | 2746968 | p.Gly211Trp | missense_variant | 0.25 |
folC | 2747200 | c.399G>T | synonymous_variant | 0.25 |
pepQ | 2859482 | p.Ala313Thr | missense_variant | 0.4 |
pepQ | 2860487 | c.-69G>T | upstream_gene_variant | 0.22 |
ribD | 2986658 | c.-180delG | upstream_gene_variant | 0.2 |
ribD | 2986693 | c.-146C>A | upstream_gene_variant | 0.22 |
ribD | 2987230 | p.Ala131Glu | missense_variant | 0.17 |
Rv2752c | 3064520 | p.Val558Leu | missense_variant | 0.17 |
Rv2752c | 3064580 | p.Gly538Cys | missense_variant | 0.15 |
Rv2752c | 3065008 | p.Pro395Gln | missense_variant | 0.18 |
Rv2752c | 3065121 | p.Lys357Asn | missense_variant | 0.2 |
Rv2752c | 3065507 | p.Ala229Thr | missense_variant | 0.18 |
Rv2752c | 3065534 | p.Pro220Thr | missense_variant | 0.2 |
Rv2752c | 3065871 | p.Phe107Leu | missense_variant | 0.14 |
thyX | 3068065 | c.-120G>T | upstream_gene_variant | 0.15 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086928 | p.Ala37Ser | missense_variant | 0.18 |
ald | 3087170 | p.Tyr117* | stop_gained | 0.15 |
ald | 3087668 | c.849C>T | synonymous_variant | 0.25 |
fbiD | 3339412 | p.Ala99Ser | missense_variant | 0.18 |
fbiD | 3339438 | c.321C>A | synonymous_variant | 0.17 |
fbiD | 3339476 | p.Leu120* | stop_gained | 0.18 |
fbiD | 3339624 | c.507G>A | synonymous_variant | 0.22 |
fbiD | 3339732 | c.615C>T | synonymous_variant | 0.18 |
Rv3083 | 3448534 | p.Gly11Cys | missense_variant | 0.22 |
Rv3083 | 3448798 | p.His99Asn | missense_variant | 0.18 |
Rv3083 | 3448823 | p.Ala107Asp | missense_variant | 0.27 |
Rv3083 | 3449005 | p.His168Asn | missense_variant | 0.18 |
Rv3083 | 3449331 | c.828C>A | synonymous_variant | 0.29 |
fprA | 3473809 | c.-198G>T | upstream_gene_variant | 0.2 |
fprA | 3473854 | c.-153G>T | upstream_gene_variant | 0.17 |
fprA | 3473874 | c.-133C>A | upstream_gene_variant | 0.2 |
fprA | 3473953 | c.-54C>A | upstream_gene_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474424 | p.Gln140* | stop_gained | 0.33 |
fprA | 3474476 | p.Asn157Thr | missense_variant | 0.29 |
whiB7 | 3568786 | c.-107C>A | upstream_gene_variant | 0.19 |
whiB7 | 3568834 | c.-155G>T | upstream_gene_variant | 0.17 |
Rv3236c | 3612118 | c.999G>C | synonymous_variant | 0.18 |
Rv3236c | 3612167 | p.Gly317Val | missense_variant | 0.22 |
Rv3236c | 3612495 | c.622C>A | synonymous_variant | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613012 | c.105G>T | synonymous_variant | 0.15 |
Rv3236c | 3613068 | p.Val17Leu | missense_variant | 0.17 |
fbiA | 3640354 | c.-189C>T | upstream_gene_variant | 0.15 |
fbiB | 3640584 | c.-951C>A | upstream_gene_variant | 0.22 |
fbiA | 3641513 | p.Cys324Phe | missense_variant | 0.17 |
fbiB | 3641564 | c.30G>T | synonymous_variant | 0.2 |
fbiB | 3641963 | c.429C>A | synonymous_variant | 0.29 |
alr | 3840320 | c.1101G>T | synonymous_variant | 0.2 |
alr | 3840577 | p.Ala282Ser | missense_variant | 0.2 |
alr | 3840602 | c.819G>T | synonymous_variant | 0.18 |
alr | 3841132 | p.Ala97Ser | missense_variant | 0.2 |
alr | 3841465 | c.-45G>T | upstream_gene_variant | 0.22 |
alr | 3841466 | c.-46A>G | upstream_gene_variant | 0.25 |
alr | 3841619 | c.-199G>T | upstream_gene_variant | 0.15 |
rpoA | 3877490 | p.Asp340Tyr | missense_variant | 0.17 |
rpoA | 3877499 | p.Asp337Tyr | missense_variant | 0.2 |
rpoA | 3877533 | c.975C>A | synonymous_variant | 0.2 |
rpoA | 3878030 | p.Gly160Trp | missense_variant | 0.27 |
rpoA | 3878532 | c.-25G>T | upstream_gene_variant | 0.4 |
ddn | 3986646 | c.-198C>A | upstream_gene_variant | 0.18 |
clpC1 | 4038629 | c.2076G>T | synonymous_variant | 0.18 |
clpC1 | 4038779 | c.1926C>T | synonymous_variant | 0.25 |
clpC1 | 4038946 | p.Asp587Tyr | missense_variant | 1.0 |
clpC1 | 4038951 | p.Phe585Ser | missense_variant | 1.0 |
clpC1 | 4038988 | p.Asp573Tyr | missense_variant | 0.4 |
clpC1 | 4040183 | p.Phe174Leu | missense_variant | 0.2 |
clpC1 | 4040212 | p.Pro165Thr | missense_variant | 0.18 |
clpC1 | 4040317 | p.Glu130* | stop_gained | 0.2 |
clpC1 | 4040374 | p.Gly111Cys | missense_variant | 0.25 |
panD | 4043995 | p.Ala96Asp | missense_variant | 0.2 |
panD | 4044003 | p.Met93Ile | missense_variant | 0.17 |
panD | 4044125 | p.Ala53Ser | missense_variant | 0.15 |
embC | 4239921 | p.Arg20Leu | missense_variant | 0.22 |
embC | 4240287 | p.Ala142Asp | missense_variant | 0.17 |
embC | 4240582 | c.720C>A | synonymous_variant | 0.29 |
embC | 4240792 | p.Met310Ile | missense_variant | 0.2 |
embC | 4240932 | p.Trp357Leu | missense_variant | 0.33 |
embC | 4241491 | c.1629G>T | synonymous_variant | 0.17 |
embC | 4241707 | c.1845G>T | synonymous_variant | 0.15 |
embC | 4242155 | p.Met765Val | missense_variant | 0.11 |
embA | 4242313 | c.-920C>A | upstream_gene_variant | 0.3 |
embA | 4242637 | c.-596C>A | upstream_gene_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243292 | c.60G>T | synonymous_variant | 0.22 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244135 | p.Glu301Asp | missense_variant | 0.2 |
embA | 4244243 | c.1011G>T | synonymous_variant | 0.2 |
embA | 4244325 | p.Gly365Cys | missense_variant | 0.22 |
embA | 4244405 | c.1173C>A | synonymous_variant | 0.25 |
embA | 4244426 | c.1194G>T | synonymous_variant | 0.17 |
embA | 4244571 | c.1339C>A | synonymous_variant | 0.2 |
embA | 4244789 | c.1557C>T | synonymous_variant | 0.2 |
embA | 4245320 | c.2088C>A | synonymous_variant | 0.33 |
embA | 4245921 | p.Gly897Cys | missense_variant | 0.17 |
embA | 4245939 | p.Gly903Cys | missense_variant | 0.17 |
embB | 4246466 | c.-48G>T | upstream_gene_variant | 0.18 |
embB | 4246646 | p.Pro45Thr | missense_variant | 0.18 |
embB | 4247183 | p.Gly224Arg | missense_variant | 0.25 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.17 |
embB | 4247896 | c.1383G>T | synonymous_variant | 0.25 |
embB | 4248039 | p.Arg509Leu | missense_variant | 0.15 |
embB | 4248076 | p.Glu521Asp | missense_variant | 0.18 |
embB | 4248091 | p.Tyr526* | stop_gained | 0.22 |
embB | 4248598 | c.2085A>G | synonymous_variant | 0.12 |
aftB | 4267127 | c.1710G>T | synonymous_variant | 0.2 |
aftB | 4267551 | p.Tyr429Cys | missense_variant | 0.15 |
aftB | 4267574 | c.1263G>T | synonymous_variant | 0.17 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268881 | c.-45C>A | upstream_gene_variant | 0.18 |
aftB | 4269699 | c.-863C>A | upstream_gene_variant | 0.15 |
ethA | 4326033 | p.Ala481Ser | missense_variant | 0.15 |
ethA | 4327323 | p.Pro51Thr | missense_variant | 0.2 |
ethA | 4327458 | p.Asp6Asn | missense_variant | 0.25 |
whiB6 | 4338371 | p.Thr51Pro | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408200 | c.3G>T | start_lost | 0.15 |
gid | 4408218 | c.-16G>T | upstream_gene_variant | 0.14 |