Run ID: ERR3509870
Sample name:
Date: 01-04-2023 02:32:54
Number of reads: 309700
Percentage reads mapped: 99.61
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 | 0.46 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.38 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761139 | p.His445Tyr | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embA | 4243222 | c.-11C>A | upstream_gene_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6142 | c.903G>T | synonymous_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491379 | c.597C>T | synonymous_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.43 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763500 | c.132delC | frameshift_variant | 0.12 |
rpoC | 765687 | p.Ala773Glu | missense_variant | 0.13 |
rpoC | 766780 | p.Glu1137Asp | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775678 | p.Lys935Glu | missense_variant | 0.1 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 778621 | c.-141G>A | upstream_gene_variant | 0.2 |
mmpR5 | 779350 | p.Gly121Trp | missense_variant | 0.22 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304006 | p.Pro359Gln | missense_variant | 0.14 |
Rv1258c | 1406607 | p.Val245Ala | missense_variant | 0.18 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407097 | p.Ser82Thr | missense_variant | 0.17 |
embR | 1416397 | p.Asp317Glu | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1674109 | p.Leu224Met | missense_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102686 | c.357G>T | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169559 | p.Phe352Leu | missense_variant | 0.12 |
PPE35 | 2170516 | p.Gly33Arg | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288784 | p.Thr153Ile | missense_variant | 1.0 |
pncA | 2289745 | c.-504C>T | upstream_gene_variant | 0.4 |
eis | 2714169 | c.1164G>T | synonymous_variant | 0.12 |
eis | 2714191 | p.Gln381Leu | missense_variant | 0.13 |
eis | 2715470 | c.-138G>T | upstream_gene_variant | 0.1 |
folC | 2746787 | p.Ala271Gly | missense_variant | 0.14 |
pepQ | 2860615 | c.-197T>C | upstream_gene_variant | 0.22 |
thyX | 3067381 | p.Tyr189His | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641974 | p.Val147Asp | missense_variant | 0.17 |
fbiB | 3642205 | p.Asp224Gly | missense_variant | 1.0 |
fbiB | 3642789 | p.Glu419* | stop_gained | 0.13 |
alr | 3840415 | p.Pro336Thr | missense_variant | 0.17 |
rpoA | 3878231 | p.Val93Ile | missense_variant | 0.11 |
clpC1 | 4040070 | p.Pro212Leu | missense_variant | 0.11 |
clpC1 | 4040130 | p.Gly192Val | missense_variant | 0.11 |
embC | 4239715 | c.-148G>A | upstream_gene_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244276 | c.1044A>G | synonymous_variant | 0.15 |
embA | 4245142 | p.Ile637Thr | missense_variant | 0.12 |
embA | 4245934 | p.Pro901Arg | missense_variant | 0.12 |
embB | 4246567 | c.54G>T | synonymous_variant | 1.0 |
embB | 4247108 | p.Gly199Arg | missense_variant | 0.15 |
embB | 4248422 | p.Ala637Ser | missense_variant | 0.11 |
aftB | 4267647 | p.Asp397Gly | 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 |