Run ID: SRR11972159
Sample name:
Date: 03-04-2023 05:30:23
Number of reads: 533754
Percentage reads mapped: 98.41
Strain: lineage2.2.1
Drug-resistance: MDR-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 |
---|---|---|---|---|---|
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 | 2288936 | c.305delC | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6852 | p.Gln538Leu | missense_variant | 0.15 |
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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575427 | p.Ser27Leu | missense_variant | 0.17 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620402 | p.Trp171* | stop_gained | 0.22 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760249 | c.446dupG | frameshift_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776087 | c.2394C>G | synonymous_variant | 0.25 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776342 | c.2139G>A | synonymous_variant | 0.33 |
mmpR5 | 779428 | p.Glu147* | stop_gained | 0.25 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781926 | p.Lys123Glu | missense_variant | 0.14 |
fbiC | 1303383 | c.453G>A | synonymous_variant | 0.17 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1417514 | c.-167C>T | upstream_gene_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472193 | n.348A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472373 | n.528G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472374 | n.529T>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472591 | n.746G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472601 | n.756G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472819 | n.974T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472954 | n.1110delC | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472958 | n.1113_1114insC | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472986 | n.1141_1142insA | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472989 | n.1145delA | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.14 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.15 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.15 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.15 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834691 | p.Tyr384Asp | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102074 | p.Met323Lys | missense_variant | 0.13 |
ndh | 2103090 | c.-48G>T | upstream_gene_variant | 0.12 |
ndh | 2103158 | c.-116C>A | upstream_gene_variant | 0.14 |
katG | 2154149 | p.Asn655Asp | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.29 |
PPE35 | 2167760 | c.2853G>A | synonymous_variant | 0.29 |
PPE35 | 2167763 | p.Ile950Val | missense_variant | 0.29 |
PPE35 | 2167784 | c.2829C>T | synonymous_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168213 | c.2400G>A | synonymous_variant | 0.14 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.14 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.29 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.29 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.19 |
PPE35 | 2170157 | p.Ala152Ser | missense_variant | 0.13 |
PPE35 | 2170164 | p.Ala150Val | missense_variant | 0.12 |
PPE35 | 2170220 | c.393C>G | synonymous_variant | 0.12 |
PPE35 | 2170223 | c.390T>C | synonymous_variant | 0.12 |
PPE35 | 2170238 | c.375T>G | synonymous_variant | 0.15 |
PPE35 | 2170247 | p.Ile122Met | missense_variant | 0.12 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.18 |
PPE35 | 2170540 | c.73C>T | synonymous_variant | 0.18 |
Rv1979c | 2222032 | c.1132delG | frameshift_variant | 0.13 |
Rv1979c | 2222723 | c.442C>T | synonymous_variant | 0.67 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289262 | c.-21G>T | upstream_gene_variant | 0.2 |
pncA | 2289742 | c.-501G>A | upstream_gene_variant | 0.15 |
eis | 2715222 | c.111G>A | synonymous_variant | 0.15 |
eis | 2715425 | c.-93G>T | upstream_gene_variant | 0.12 |
folC | 2746241 | p.Asp453Gly | missense_variant | 0.4 |
Rv2752c | 3064969 | p.Lys408Arg | missense_variant | 0.22 |
thyA | 3074207 | p.Glu89Lys | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339058 | c.-60G>A | upstream_gene_variant | 0.15 |
fbiD | 3339339 | c.222G>T | synonymous_variant | 0.25 |
fbiD | 3339738 | c.621C>A | synonymous_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3642615 | p.Pro361Thr | missense_variant | 0.33 |
alr | 3840813 | p.Pro203His | missense_variant | 0.14 |
alr | 3841442 | c.-22G>A | upstream_gene_variant | 0.14 |
rpoA | 3877806 | c.702C>T | synonymous_variant | 0.17 |
rpoA | 3877969 | p.Ala180Val | missense_variant | 1.0 |
ddn | 3986822 | c.-22C>A | upstream_gene_variant | 0.14 |
clpC1 | 4039177 | p.Met510Leu | missense_variant | 0.15 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.12 |
panD | 4044393 | c.-112G>A | upstream_gene_variant | 0.33 |
embC | 4240456 | c.594C>T | synonymous_variant | 0.14 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.18 |
embC | 4240793 | p.Ala311Ser | missense_variant | 0.22 |
embC | 4240801 | c.939C>T | synonymous_variant | 0.17 |
embC | 4240803 | p.Tyr314Phe | missense_variant | 0.17 |
embC | 4240853 | c.991C>T | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244816 | c.1584G>A | synonymous_variant | 1.0 |
embB | 4246481 | c.-33C>T | upstream_gene_variant | 0.29 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.5 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.67 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.6 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.6 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.29 |
embB | 4247854 | c.1341C>A | synonymous_variant | 0.2 |
aftB | 4267149 | p.Glu563Val | missense_variant | 0.2 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.9 |
aftB | 4268640 | p.Leu66Gln | missense_variant | 0.33 |
ethR | 4328011 | p.Ala155Pro | missense_variant | 0.17 |
ethA | 4328275 | c.-802G>A | upstream_gene_variant | 0.22 |
whiB6 | 4338394 | p.Thr43Met | 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 |