Run ID: SRR11972192
Sample name:
Date: 03-04-2023 05:31:25
Number of reads: 198122
Percentage reads mapped: 99.1
Strain: lineage2.2.1.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 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 |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ethA | 4326250 | p.Tyr408* | stop_gained | 0.18 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5791 | c.552A>G | synonymous_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7454 | c.153G>A | synonymous_variant | 0.15 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9301 | p.Ala667Asp | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491635 | p.Ile285Val | missense_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491758 | p.Ser326Pro | missense_variant | 0.25 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620166 | c.276G>A | synonymous_variant | 0.33 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759624 | c.-183G>A | upstream_gene_variant | 0.13 |
rpoB | 760341 | p.Val179Met | missense_variant | 0.12 |
rpoB | 762913 | p.His1036Arg | missense_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765942 | p.Lys858Arg | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777462 | p.Ala340Val | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781622 | c.63C>G | synonymous_variant | 0.5 |
rplC | 801238 | p.Val144Met | missense_variant | 0.25 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461098 | c.54C>T | synonymous_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473001 | n.1156G>A | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1673609 | p.Gly57Asp | missense_variant | 0.18 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168320 | p.Thr765Ser | missense_variant | 0.22 |
PPE35 | 2169638 | c.975T>A | synonymous_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289799 | c.-558G>A | upstream_gene_variant | 0.18 |
pncA | 2289889 | c.-648C>A | upstream_gene_variant | 0.2 |
kasA | 2518794 | p.Ser227Cys | missense_variant | 0.17 |
eis | 2714190 | c.1143G>A | synonymous_variant | 0.2 |
eis | 2714427 | c.906G>A | synonymous_variant | 0.14 |
eis | 2714635 | p.Leu233His | missense_variant | 0.15 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
folC | 2747725 | c.-127C>T | upstream_gene_variant | 0.18 |
pepQ | 2860404 | c.15G>A | synonymous_variant | 0.29 |
thyA | 3073896 | c.576C>A | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448578 | c.75C>T | synonymous_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475252 | p.Lys416* | stop_gained | 0.25 |
whiB7 | 3568610 | p.Asp24Asn | missense_variant | 0.13 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641153 | p.Ala204Val | missense_variant | 0.67 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.15 |
rpoA | 3878041 | p.Gly156Asp | missense_variant | 0.15 |
clpC1 | 4038563 | p.Asp714Glu | missense_variant | 0.12 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.4 |
clpC1 | 4040362 | p.Glu115Lys | missense_variant | 0.17 |
clpC1 | 4040870 | c.-166T>A | upstream_gene_variant | 0.22 |
embC | 4239887 | p.Arg9Cys | missense_variant | 0.33 |
embC | 4239936 | p.Asn25Ser | missense_variant | 0.4 |
embC | 4240655 | p.Ala265Thr | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243190 | c.-43G>C | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4246372 | p.Arg1047His | missense_variant | 1.0 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269736 | p.Leu33Pro | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407600 | c.603C>A | synonymous_variant | 0.17 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408187 | p.Pro6Ala | missense_variant | 0.22 |