Run ID: SRR11972223
Sample name:
Date: 03-04-2023 05:32:32
Number of reads: 466113
Percentage reads mapped: 98.97
Strain: lineage2.2.1.1
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 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 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 |
inhA | 1674248 | p.Ile16Thr | missense_variant | 0.18 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5119 | c.-121T>A | upstream_gene_variant | 0.17 |
gyrB | 6136 | c.897G>A | synonymous_variant | 0.12 |
gyrB | 6810 | p.Tyr524Phe | missense_variant | 0.14 |
gyrB | 7170 | p.Ala644Asp | missense_variant | 0.13 |
gyrA | 7186 | c.-116C>T | upstream_gene_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 |
gyrA | 9406 | p.Gly702Val | missense_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759939 | p.Pro45Thr | missense_variant | 1.0 |
rpoB | 761378 | c.1572C>T | synonymous_variant | 1.0 |
rpoB | 761579 | c.1773G>A | synonymous_variant | 0.13 |
rpoB | 762652 | p.Trp949* | stop_gained | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764459 | p.Glu364* | stop_gained | 0.12 |
rpoC | 766248 | p.Val960Ala | missense_variant | 0.12 |
rpoC | 766315 | c.2946C>A | synonymous_variant | 0.15 |
rpoC | 766996 | c.3627C>A | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777433 | p.Ala350Thr | missense_variant | 0.17 |
mmpL5 | 778086 | c.394delG | frameshift_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781411 | c.-149G>T | upstream_gene_variant | 0.15 |
fbiC | 1303486 | p.Gly186Arg | missense_variant | 0.15 |
fbiC | 1304354 | p.Ser475Leu | missense_variant | 0.13 |
Rv1258c | 1406227 | p.Asp372Asn | missense_variant | 0.12 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461236 | p.Tyr64* | stop_gained | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472249 | n.404T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473461 | n.-197T>C | upstream_gene_variant | 0.15 |
rrl | 1474553 | n.896T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474980 | n.1323G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475156 | n.1499G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.11 |
inhA | 1674138 | c.-64C>T | upstream_gene_variant | 0.12 |
inhA | 1674759 | c.558G>A | synonymous_variant | 0.4 |
rpsA | 1833504 | c.-38T>C | upstream_gene_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918217 | p.Thr93Ile | missense_variant | 0.15 |
ndh | 2101988 | p.Ala352Val | missense_variant | 0.18 |
ndh | 2102133 | p.Gln304Lys | missense_variant | 0.12 |
ndh | 2102914 | c.129C>T | synonymous_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155280 | p.Ala278Thr | missense_variant | 0.18 |
katG | 2155431 | c.681G>A | synonymous_variant | 0.18 |
PPE35 | 2167821 | p.Ser931* | stop_gained | 0.14 |
PPE35 | 2167833 | p.Leu927Arg | missense_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167930 | p.Ser895Pro | missense_variant | 0.17 |
PPE35 | 2169238 | p.Asp459Asn | missense_variant | 0.17 |
PPE35 | 2169464 | c.1149C>T | synonymous_variant | 0.14 |
PPE35 | 2169534 | p.Gly360Val | missense_variant | 0.12 |
PPE35 | 2169542 | c.1071C>T | synonymous_variant | 0.12 |
Rv1979c | 2222660 | p.Gly169Cys | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289385 | c.-144C>T | upstream_gene_variant | 0.17 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
folC | 2746145 | p.Asp485Gly | missense_variant | 0.18 |
folC | 2746249 | c.1350C>T | synonymous_variant | 0.12 |
Rv2752c | 3065184 | c.1008G>A | synonymous_variant | 0.13 |
Rv2752c | 3065357 | p.Leu279Val | missense_variant | 0.18 |
Rv2752c | 3066303 | c.-112C>A | upstream_gene_variant | 0.15 |
thyA | 3074034 | c.438T>C | synonymous_variant | 0.18 |
thyA | 3074496 | c.-25C>T | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339376 | p.Asp87Tyr | missense_variant | 0.2 |
Rv3083 | 3448305 | c.-199T>C | upstream_gene_variant | 0.12 |
Rv3083 | 3448512 | p.Gln3His | missense_variant | 0.13 |
Rv3083 | 3449052 | c.549C>T | synonymous_variant | 0.18 |
Rv3083 | 3449290 | p.Lys263* | stop_gained | 0.15 |
Rv3083 | 3449987 | p.Ala495Gly | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474143 | p.Trp46Tyr | missense_variant | 0.25 |
Rv3236c | 3612699 | p.Leu140Met | missense_variant | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3642540 | p.Ala336Thr | missense_variant | 0.15 |
alr | 3840648 | p.Tyr258Cys | missense_variant | 0.12 |
alr | 3841067 | c.354C>A | synonymous_variant | 0.18 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.26 |
rpoA | 3877505 | p.Ala335Ser | missense_variant | 0.15 |
rpoA | 3877598 | c.910C>T | synonymous_variant | 0.17 |
rpoA | 3878090 | p.Val140Ile | missense_variant | 0.2 |
ddn | 3986860 | p.Pro6Leu | missense_variant | 0.13 |
clpC1 | 4038502 | p.Ile735Phe | missense_variant | 0.15 |
clpC1 | 4039509 | p.Ala399Val | missense_variant | 0.22 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.13 |
clpC1 | 4039738 | p.Thr323Ala | missense_variant | 0.12 |
clpC1 | 4040416 | p.Gln97Lys | missense_variant | 0.11 |
clpC1 | 4040638 | p.Leu23Val | missense_variant | 0.12 |
panD | 4043870 | p.Val138Leu | missense_variant | 0.12 |
panD | 4044271 | p.Thr4Met | missense_variant | 0.11 |
embC | 4240475 | p.Ala205Thr | missense_variant | 0.13 |
embC | 4241174 | p.Ser438Pro | missense_variant | 0.14 |
embC | 4241905 | c.2043C>T | synonymous_variant | 0.13 |
embC | 4242207 | p.Ser782Phe | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4246059 | p.Ala943Ser | missense_variant | 0.2 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.25 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.21 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.2 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.2 |
embB | 4247867 | p.Val452Met | missense_variant | 0.12 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
embB | 4249062 | p.Thr850Ile | missense_variant | 0.12 |
aftB | 4267285 | p.Thr518Ala | missense_variant | 0.11 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4327137 | p.Glu113Lys | missense_variant | 0.2 |
whiB6 | 4338250 | p.Ala91Glu | missense_variant | 0.14 |
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 |