Run ID: ERR6336759
Sample name:
Date: 02-04-2023 02:02:23
Number of reads: 1635318
Percentage reads mapped: 98.95
Strain: lineage1.2.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 1.0 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 1.0 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2288727 | p.Leu172Pro | missense_variant | 0.13 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5518 | p.Ile93Met | missense_variant | 0.13 |
gyrB | 5523 | p.Thr95Ile | missense_variant | 0.13 |
gyrB | 5538 | p.Met100Thr | missense_variant | 0.1 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575337 | c.-11T>C | upstream_gene_variant | 0.17 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 575373 | p.Gly9Asp | missense_variant | 0.12 |
mshA | 575538 | p.Asp64Gly | missense_variant | 0.12 |
mshA | 575620 | c.273G>T | synonymous_variant | 0.13 |
mshA | 575621 | p.Ala92Ser | missense_variant | 0.13 |
mshA | 576506 | p.Gly387Ser | missense_variant | 0.25 |
mshA | 576781 | c.1434G>A | synonymous_variant | 0.22 |
ccsA | 619859 | c.-32G>A | upstream_gene_variant | 0.15 |
ccsA | 620122 | p.Arg78Trp | missense_variant | 0.5 |
ccsA | 620276 | p.Leu129Pro | missense_variant | 0.15 |
ccsA | 620301 | c.411G>A | synonymous_variant | 0.14 |
rpoB | 762697 | p.Ala964Val | missense_variant | 0.15 |
rpoB | 762702 | p.Val966Met | missense_variant | 0.15 |
rpoB | 762807 | p.Lys1001Glu | missense_variant | 0.4 |
rpoC | 762986 | c.-384G>A | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.97 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764532 | p.Gly388Ala | missense_variant | 0.18 |
rpoC | 764535 | p.Arg389Gln | missense_variant | 0.22 |
rpoC | 764649 | p.Arg427Gln | missense_variant | 0.14 |
rpoC | 765275 | p.Arg636Trp | missense_variant | 0.14 |
rpoC | 765548 | p.Ser727Gly | missense_variant | 0.2 |
rpoC | 765933 | p.Gly855Val | missense_variant | 0.12 |
rpoC | 765969 | p.Thr867Ile | missense_variant | 0.15 |
rpoC | 766162 | c.2793C>T | synonymous_variant | 0.17 |
rpoC | 766403 | p.Met1012Leu | missense_variant | 0.12 |
rpoC | 766527 | p.Val1053Ala | missense_variant | 0.13 |
rpoC | 766998 | p.Ile1210Thr | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777312 | p.Pro390Leu | missense_variant | 0.22 |
mmpL5 | 777634 | p.Gly283Ser | missense_variant | 0.25 |
mmpL5 | 777665 | c.816G>A | synonymous_variant | 0.18 |
mmpL5 | 777961 | p.Glu174Lys | missense_variant | 0.17 |
mmpR5 | 779380 | p.Gln131* | stop_gained | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303093 | c.164delT | frameshift_variant | 0.17 |
fbiC | 1303400 | p.Gln157Arg | missense_variant | 0.12 |
fbiC | 1303536 | c.606G>A | synonymous_variant | 0.12 |
fbiC | 1303564 | p.Gly212Ser | missense_variant | 0.14 |
fbiC | 1304439 | p.Glu503Asp | missense_variant | 0.5 |
fbiC | 1304817 | p.His629Gln | missense_variant | 0.11 |
fbiC | 1305216 | c.2286C>T | synonymous_variant | 0.5 |
Rv1258c | 1406262 | p.Gly360Asp | missense_variant | 0.18 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406718 | p.Leu208Trp | missense_variant | 0.11 |
Rv1258c | 1406773 | p.Ala190Thr | missense_variant | 0.14 |
Rv1258c | 1407005 | c.336G>A | synonymous_variant | 0.33 |
embR | 1416408 | p.His314Tyr | missense_variant | 0.13 |
embR | 1416429 | p.Ala307Thr | missense_variant | 0.15 |
embR | 1416930 | p.Ala140Thr | missense_variant | 0.13 |
embR | 1416999 | p.Ala117Thr | missense_variant | 0.17 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
inhA | 1673561 | c.-641A>G | upstream_gene_variant | 0.15 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
inhA | 1674813 | c.612C>T | synonymous_variant | 0.18 |
rpsA | 1833358 | c.-184C>T | upstream_gene_variant | 1.0 |
rpsA | 1834499 | c.958C>T | synonymous_variant | 0.13 |
rpsA | 1834562 | p.Gly341Ser | missense_variant | 0.13 |
rpsA | 1834865 | p.Gly442Arg | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918158 | c.219G>A | synonymous_variant | 0.13 |
tlyA | 1918587 | p.Gln216His | missense_variant | 0.29 |
tlyA | 1918598 | p.Trp220* | stop_gained | 0.4 |
ndh | 2102006 | p.Thr346Arg | missense_variant | 0.11 |
ndh | 2102040 | p.Gly335Ser | missense_variant | 0.12 |
ndh | 2102266 | c.777C>T | synonymous_variant | 0.13 |
ndh | 2103188 | c.-146T>A | upstream_gene_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155296 | p.Phe272Leu | missense_variant | 0.1 |
katG | 2155744 | p.Gly123Ala | missense_variant | 0.5 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170491 | p.Ala41Val | missense_variant | 0.17 |
PPE35 | 2170533 | p.Ala27Val | missense_variant | 0.14 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223330 | c.-166C>A | upstream_gene_variant | 0.25 |
pncA | 2288695 | p.Val183Ile | missense_variant | 0.13 |
pncA | 2289146 | p.Ser32Arg | missense_variant | 0.25 |
pncA | 2289462 | c.-221C>T | upstream_gene_variant | 0.13 |
pncA | 2289897 | c.-656G>A | upstream_gene_variant | 0.15 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518411 | c.297C>G | synonymous_variant | 0.11 |
kasA | 2518633 | c.519G>C | synonymous_variant | 0.2 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
kasA | 2519115 | p.Ala334Val | missense_variant | 0.25 |
kasA | 2519234 | p.Glu374Lys | missense_variant | 0.18 |
eis | 2714314 | p.Cys340Tyr | missense_variant | 0.17 |
eis | 2714967 | c.366G>A | synonymous_variant | 0.18 |
eis | 2715056 | p.Arg93Trp | missense_variant | 0.17 |
eis | 2715172 | p.Pro54Leu | missense_variant | 0.18 |
eis | 2715362 | c.-30T>A | upstream_gene_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726716 | p.Ala175Val | missense_variant | 0.17 |
folC | 2746275 | p.Val442Ile | missense_variant | 0.17 |
folC | 2746498 | c.1101G>A | synonymous_variant | 0.12 |
folC | 2746515 | c.1084C>T | synonymous_variant | 0.13 |
folC | 2746651 | c.948T>C | synonymous_variant | 0.5 |
folC | 2746678 | c.921T>G | synonymous_variant | 0.12 |
folC | 2746870 | c.729G>A | synonymous_variant | 0.13 |
pepQ | 2859781 | p.Gln213Arg | missense_variant | 0.12 |
pepQ | 2859785 | p.Leu212Val | missense_variant | 0.17 |
pepQ | 2860124 | p.Ser99Cys | missense_variant | 0.4 |
pepQ | 2860153 | p.Glu89Val | missense_variant | 0.33 |
pepQ | 2860157 | p.Gly88Ser | missense_variant | 0.33 |
ribD | 2987076 | p.Val80Ile | missense_variant | 0.13 |
ribD | 2987095 | p.Gly86Asp | missense_variant | 0.18 |
ribD | 2987457 | p.Val207Met | missense_variant | 0.13 |
ribD | 2987512 | p.Arg225His | missense_variant | 0.2 |
Rv2752c | 3066246 | c.-55G>A | upstream_gene_variant | 0.12 |
Rv2752c | 3066275 | c.-84G>A | upstream_gene_variant | 0.22 |
Rv2752c | 3066387 | c.-197delC | upstream_gene_variant | 0.14 |
Rv2752c | 3067144 | c.-953G>C | upstream_gene_variant | 0.11 |
thyX | 3067348 | p.Ala200Thr | missense_variant | 0.25 |
thyX | 3067372 | p.Trp192Arg | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087818 | p.Cys333Trp | missense_variant | 0.29 |
fbiD | 3339023 | c.-95G>C | upstream_gene_variant | 0.22 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
Rv3083 | 3448319 | c.-185C>G | upstream_gene_variant | 0.18 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448972 | p.His157Tyr | missense_variant | 0.13 |
Rv3083 | 3449194 | p.Gly231Ser | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474040 | p.Gly12Arg | missense_variant | 0.18 |
fprA | 3474061 | p.Ala19Thr | missense_variant | 0.18 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475044 | c.1038C>T | synonymous_variant | 0.12 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
Rv3236c | 3612020 | p.Gly366Val | missense_variant | 0.12 |
Rv3236c | 3612089 | p.Leu343Pro | missense_variant | 0.14 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiA | 3640820 | p.Val93Gly | missense_variant | 0.14 |
fbiA | 3641172 | p.Met210Ile | missense_variant | 0.15 |
fbiA | 3641533 | p.Ala331Thr | missense_variant | 0.17 |
alr | 3840484 | p.Gly313Ser | missense_variant | 0.25 |
alr | 3840623 | c.798C>T | synonymous_variant | 0.17 |
alr | 3840666 | p.Arg252Gln | missense_variant | 0.18 |
rpoA | 3877771 | p.Ser246* | stop_gained | 0.11 |
rpoA | 3878566 | c.-59C>T | upstream_gene_variant | 0.18 |
rpoA | 3878567 | c.-60C>A | upstream_gene_variant | 0.18 |
ddn | 3987041 | c.198C>T | synonymous_variant | 0.17 |
clpC1 | 4038171 | p.Pro845Arg | missense_variant | 0.22 |
clpC1 | 4039627 | p.Lys360Glu | missense_variant | 0.11 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4239707 | c.-156C>G | upstream_gene_variant | 0.12 |
embC | 4240190 | p.Pro110Ala | missense_variant | 0.13 |
embC | 4240524 | p.Arg221His | missense_variant | 0.14 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241097 | p.Ser412Leu | missense_variant | 0.2 |
embC | 4241717 | p.Arg619Trp | missense_variant | 0.67 |
embC | 4242494 | p.Asp878His | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242756 | p.Ile965Asn | missense_variant | 0.18 |
embC | 4243131 | p.Pro1090Leu | missense_variant | 0.18 |
embA | 4243407 | p.Thr59Ala | missense_variant | 0.12 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4244262 | p.Leu344Met | missense_variant | 0.25 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4244474 | c.1242G>C | synonymous_variant | 0.2 |
embA | 4244477 | c.1245G>C | synonymous_variant | 0.29 |
embA | 4244968 | p.Gly579Val | missense_variant | 0.12 |
embA | 4245420 | c.2188C>T | synonymous_variant | 0.2 |
embA | 4245507 | p.Gly759Arg | missense_variant | 0.33 |
embB | 4245584 | c.-930C>T | upstream_gene_variant | 0.12 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246336 | p.Ala1035Val | missense_variant | 0.12 |
embA | 4246471 | p.Thr1080Ile | missense_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.67 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.5 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.25 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.2 |
embB | 4246588 | c.75G>A | synonymous_variant | 0.22 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247705 | p.Phe398Ile | missense_variant | 0.17 |
embB | 4247924 | p.Arg471Cys | missense_variant | 0.4 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.25 |
embB | 4249222 | c.2709C>T | synonymous_variant | 0.17 |
embB | 4249397 | p.Ala962Thr | missense_variant | 1.0 |
aftB | 4266960 | p.Arg626Gln | missense_variant | 0.13 |
aftB | 4268246 | c.591G>A | synonymous_variant | 0.2 |
aftB | 4268344 | p.Arg165Gly | missense_variant | 0.25 |
aftB | 4268405 | c.432G>A | synonymous_variant | 0.2 |
aftB | 4268445 | p.Ala131Val | missense_variant | 0.17 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.15 |
ubiA | 4269223 | p.Ala204Val | missense_variant | 0.12 |
aftB | 4269225 | c.-389C>G | upstream_gene_variant | 0.12 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269591 | c.-755C>T | upstream_gene_variant | 0.2 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
ethA | 4328154 | c.-681C>T | upstream_gene_variant | 0.14 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |