Run ID: ERR8665583
Sample name:
Date: 02-04-2023 07:32:45
Number of reads: 470619
Percentage reads mapped: 99.56
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 |
rpoC | 764841 | p.Ile491Thr | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289040 | p.Trp68Gly | missense_variant | 1.0 | pyrazinamide |
ahpC | 2726142 | c.-51G>T | upstream_gene_variant | 0.2 | isoniazid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
ethA | 4326087 | c.1386delA | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6706 | p.Glu489Asp | missense_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8114 | c.813C>A | synonymous_variant | 0.2 |
gyrA | 8273 | c.972C>A | synonymous_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490819 | p.Glu13* | stop_gained | 0.33 |
fgd1 | 491140 | p.Gly120Cys | missense_variant | 0.33 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576502 | c.1155C>T | synonymous_variant | 0.22 |
ccsA | 619938 | p.Trp16Cys | missense_variant | 0.14 |
ccsA | 619960 | p.Ala24Ser | missense_variant | 0.13 |
ccsA | 620268 | c.378G>A | synonymous_variant | 0.17 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760648 | p.Pro281Gln | missense_variant | 0.17 |
rpoB | 762206 | c.2400C>A | synonymous_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764853 | p.Pro495Gln | missense_variant | 0.17 |
rpoC | 765247 | c.1878C>A | synonymous_variant | 0.18 |
rpoC | 766045 | p.Gln892His | missense_variant | 0.25 |
rpoC | 766083 | p.Ala905Val | missense_variant | 0.2 |
rpoC | 767001 | p.Thr1211Lys | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775676 | p.Lys935Asn | missense_variant | 0.29 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776642 | p.Met613Ile | missense_variant | 0.17 |
mmpL5 | 776738 | c.1743C>A | synonymous_variant | 0.18 |
mmpL5 | 777016 | p.Gly489Cys | missense_variant | 0.2 |
mmpL5 | 777026 | c.1455C>A | synonymous_variant | 0.14 |
mmpR5 | 778178 | c.-812G>T | upstream_gene_variant | 0.2 |
mmpL5 | 779241 | c.-761C>T | upstream_gene_variant | 0.17 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800627 | c.-182C>T | upstream_gene_variant | 0.14 |
rplC | 800757 | c.-52G>A | upstream_gene_variant | 0.25 |
rplC | 801291 | p.Phe161Leu | missense_variant | 0.18 |
rplC | 801409 | p.Arg201Ser | missense_variant | 0.18 |
fbiC | 1303157 | p.His76Arg | missense_variant | 0.15 |
Rv1258c | 1406733 | p.Ser203* | stop_gained | 0.2 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406976 | p.Thr122Met | missense_variant | 0.18 |
embR | 1416559 | p.Lys263Asn | missense_variant | 0.2 |
embR | 1417262 | p.Pro29Gln | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475118 | n.1461C>A | non_coding_transcript_exon_variant | 0.17 |
inhA | 1673967 | c.-235G>T | upstream_gene_variant | 1.0 |
inhA | 1674653 | p.Pro151Gln | missense_variant | 0.18 |
rpsA | 1833992 | p.Ser151Ala | missense_variant | 0.15 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834216 | p.Phe225Leu | missense_variant | 0.22 |
rpsA | 1834660 | p.Phe373Leu | missense_variant | 0.18 |
rpsA | 1834676 | p.Gly379Ser | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917977 | p.Arg13Leu | missense_variant | 0.4 |
tlyA | 1918243 | p.Asp102Tyr | missense_variant | 0.2 |
ndh | 2102410 | c.633G>T | synonymous_variant | 0.4 |
katG | 2154255 | c.1857C>A | synonymous_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154753 | c.1359C>A | synonymous_variant | 0.21 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168386 | p.Glu743* | stop_gained | 0.18 |
PPE35 | 2169200 | c.1413G>T | synonymous_variant | 0.17 |
PPE35 | 2170602 | p.Ser4* | stop_gained | 0.15 |
Rv1979c | 2222140 | p.Arg342Leu | missense_variant | 0.29 |
Rv1979c | 2223132 | c.33C>A | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288716 | p.Arg176Ser | missense_variant | 0.25 |
pncA | 2289249 | c.-8G>T | upstream_gene_variant | 0.14 |
pncA | 2289771 | c.-530C>A | upstream_gene_variant | 0.25 |
kasA | 2518555 | c.441C>A | synonymous_variant | 0.18 |
kasA | 2518789 | c.675G>T | synonymous_variant | 0.22 |
eis | 2714252 | p.Leu361Ile | missense_variant | 0.14 |
eis | 2715123 | c.210G>T | synonymous_variant | 0.17 |
ahpC | 2726074 | c.-119C>A | upstream_gene_variant | 0.14 |
folC | 2746455 | c.1144C>T | synonymous_variant | 0.4 |
pepQ | 2859601 | c.817delG | frameshift_variant | 0.22 |
ribD | 2986866 | p.Ala10Ser | missense_variant | 0.17 |
ribD | 2987529 | p.Pro231Ser | missense_variant | 0.29 |
thyX | 3067205 | c.741G>T | synonymous_variant | 0.22 |
thyX | 3067331 | p.Asp205Glu | missense_variant | 0.2 |
thyX | 3067720 | p.Ala76Ser | missense_variant | 0.18 |
thyA | 3073958 | p.Leu172Met | missense_variant | 0.17 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087234 | c.415C>A | synonymous_variant | 0.22 |
Rv3083 | 3448320 | c.-184G>T | upstream_gene_variant | 0.18 |
Rv3083 | 3448367 | c.-137G>T | upstream_gene_variant | 0.17 |
Rv3083 | 3448468 | c.-36C>A | upstream_gene_variant | 0.2 |
Rv3083 | 3448663 | p.Arg54Ser | missense_variant | 0.18 |
Rv3083 | 3449879 | p.Pro459Gln | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568574 | p.Leu36Ile | missense_variant | 0.17 |
whiB7 | 3568795 | c.-116A>G | upstream_gene_variant | 1.0 |
Rv3236c | 3612678 | p.Glu147* | stop_gained | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613037 | p.Arg27Pro | missense_variant | 0.33 |
fbiB | 3641981 | c.447C>A | synonymous_variant | 0.29 |
alr | 3840485 | c.936C>A | synonymous_variant | 0.19 |
alr | 3841405 | p.Glu6* | stop_gained | 0.2 |
rpoA | 3877774 | p.Ala245Glu | missense_variant | 0.25 |
ddn | 3987185 | c.342G>T | synonymous_variant | 0.19 |
clpC1 | 4040894 | c.-190G>T | upstream_gene_variant | 0.22 |
panD | 4043994 | c.288C>A | synonymous_variant | 0.25 |
embC | 4241056 | c.1194C>A | synonymous_variant | 0.25 |
embC | 4242587 | p.Gly909Arg | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243172 | c.-61G>T | upstream_gene_variant | 0.2 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244115 | c.883C>A | synonymous_variant | 0.29 |
embA | 4245507 | p.Gly759* | stop_gained | 0.17 |
embA | 4246009 | p.Arg926Leu | missense_variant | 0.29 |
embB | 4248331 | p.Met606Ile | missense_variant | 0.29 |
embB | 4249583 | p.Asp1024Tyr | missense_variant | 0.25 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268749 | p.Asp30Tyr | missense_variant | 0.2 |
ethA | 4326960 | p.Asp172Tyr | missense_variant | 0.2 |
ethA | 4327355 | p.Ser40Tyr | missense_variant | 0.22 |
ethR | 4327934 | p.Ala129Glu | missense_variant | 0.25 |
ethR | 4327961 | p.Trp138Leu | missense_variant | 0.29 |
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 | 4407768 | p.Leu145Phe | missense_variant | 0.15 |
gid | 4407827 | p.Asp126Tyr | missense_variant | 0.2 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |