Run ID: SRR6257040
Sample name:
Date: 04-04-2023 13:24:10
Number of reads: 2180946
Percentage reads mapped: 98.48
Strain: lineage2.2.1
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 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9034 | p.Arg578Gln | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490756 | c.-27T>G | upstream_gene_variant | 0.3 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575860 | c.513G>A | synonymous_variant | 0.11 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576113 | c.766C>A | synonymous_variant | 0.25 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 762348 | p.Ser848Pro | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766110 | p.Pro914Leu | missense_variant | 0.15 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779597 | c.-693delA | 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 |
fbiC | 1302920 | c.-11G>T | upstream_gene_variant | 0.11 |
fbiC | 1304131 | p.Ala401Thr | missense_variant | 0.14 |
Rv1258c | 1406626 | p.Tyr239His | missense_variant | 0.15 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416222 | p.Phe376Leu | missense_variant | 0.11 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.12 |
atpE | 1461165 | c.121C>A | synonymous_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.42 |
inhA | 1673793 | c.-409G>T | upstream_gene_variant | 0.17 |
inhA | 1674099 | c.-103G>T | upstream_gene_variant | 0.12 |
inhA | 1674297 | p.Gln32His | missense_variant | 0.17 |
inhA | 1674911 | p.Pro237Gln | missense_variant | 0.17 |
rpsA | 1833876 | p.Ala112Asp | missense_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917802 | c.-138T>C | upstream_gene_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.13 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.13 |
PPE35 | 2169717 | p.Asn299Ile | missense_variant | 0.12 |
PPE35 | 2169719 | c.894C>T | synonymous_variant | 0.11 |
PPE35 | 2169840 | p.Gly258Val | missense_variant | 0.11 |
PPE35 | 2170415 | c.198A>C | synonymous_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518529 | p.Pro139Thr | missense_variant | 0.12 |
eis | 2714476 | p.Arg286His | missense_variant | 0.12 |
eis | 2715062 | p.His91Tyr | missense_variant | 0.15 |
eis | 2715146 | p.Leu63Met | missense_variant | 0.11 |
eis | 2715462 | c.-130G>T | upstream_gene_variant | 0.12 |
folC | 2746959 | p.Gly214Arg | missense_variant | 0.2 |
folC | 2747159 | p.Pro147Gln | missense_variant | 0.11 |
folC | 2747179 | c.420T>C | synonymous_variant | 0.11 |
pepQ | 2859532 | p.His296Arg | missense_variant | 0.12 |
pepQ | 2859621 | c.798G>T | synonymous_variant | 0.14 |
Rv2752c | 3064580 | p.Gly538Cys | missense_variant | 0.14 |
thyA | 3073772 | p.Asp234Tyr | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087081 | p.Gly88Trp | missense_variant | 0.14 |
ald | 3087789 | p.Leu324Ile | missense_variant | 0.12 |
fbiD | 3339094 | c.-24G>C | upstream_gene_variant | 0.11 |
fbiD | 3339561 | c.444C>A | synonymous_variant | 0.12 |
fbiD | 3339595 | p.Pro160Thr | missense_variant | 0.12 |
fprA | 3473998 | c.-9G>A | upstream_gene_variant | 1.0 |
fprA | 3473998 | c.-10_-9insA | upstream_gene_variant | 1.0 |
fprA | 3474144 | p.Trp46Cys | missense_variant | 0.12 |
fprA | 3474452 | p.Arg149Gln | missense_variant | 0.12 |
fprA | 3474747 | p.Gln247His | missense_variant | 0.11 |
fprA | 3475128 | c.1122C>T | synonymous_variant | 0.12 |
fprA | 3475258 | p.Val418Phe | missense_variant | 0.1 |
Rv3236c | 3612052 | c.1065C>A | synonymous_variant | 0.2 |
Rv3236c | 3612192 | p.Gly309Trp | missense_variant | 0.2 |
Rv3236c | 3612444 | p.Ile225Val | missense_variant | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641820 | p.Glu96* | stop_gained | 0.25 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.12 |
rpoA | 3878626 | c.-119A>G | upstream_gene_variant | 1.0 |
rpoA | 3878639 | c.-132C>G | upstream_gene_variant | 1.0 |
embC | 4240019 | p.Asn53Asp | missense_variant | 0.15 |
embC | 4240765 | c.903C>A | synonymous_variant | 0.17 |
embC | 4240843 | c.981C>T | synonymous_variant | 0.12 |
embC | 4240847 | p.Asp329Asn | missense_variant | 0.12 |
embC | 4242444 | p.Pro861Leu | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243065 | p.Pro1068His | missense_variant | 0.12 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245066 | p.Phe612Leu | missense_variant | 0.15 |
embB | 4245524 | c.-990G>T | upstream_gene_variant | 0.15 |
embA | 4245790 | p.Thr853Asn | missense_variant | 0.13 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.15 |
embB | 4246697 | p.Gly62Trp | missense_variant | 0.12 |
embB | 4247485 | c.972C>A | synonymous_variant | 0.1 |
embB | 4247594 | p.Cys361Gly | missense_variant | 0.22 |
embB | 4249411 | c.2898G>A | synonymous_variant | 0.11 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268414 | c.423C>T | synonymous_variant | 0.12 |
aftB | 4268825 | c.12C>A | synonymous_variant | 0.11 |
ethR | 4328044 | p.Leu166Met | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407642 | p.Arg187Ser | missense_variant | 0.15 |
gid | 4407814 | p.Gly130Asp | missense_variant | 0.12 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408436 | c.-234C>A | upstream_gene_variant | 0.17 |