Run ID: SRR21277803
Sample name:
Date: 04-04-2023 01:44:09
Number of reads: 14936507
Percentage reads mapped: 98.05
Strain: lineage2.2.1
Drug-resistance: Sensitive
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 |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 | 575407 | c.60C>A | synonymous_variant | 0.12 |
mshA | 575500 | c.153G>T | synonymous_variant | 0.12 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576253 | c.906G>T | synonymous_variant | 0.12 |
mshA | 576449 | p.Pro368Lys | missense_variant | 0.12 |
mshA | 576577 | c.1230C>A | synonymous_variant | 0.18 |
mshA | 576609 | p.Ala421Val | missense_variant | 0.11 |
ccsA | 619713 | c.-178C>A | upstream_gene_variant | 0.13 |
ccsA | 619723 | c.-168G>A | upstream_gene_variant | 0.27 |
ccsA | 619813 | c.-78C>T | upstream_gene_variant | 0.25 |
ccsA | 619977 | c.87G>A | synonymous_variant | 0.11 |
ccsA | 619998 | p.Phe36Leu | missense_variant | 0.17 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761658 | p.Pro618Thr | missense_variant | 0.12 |
rpoB | 762678 | p.Leu958Ile | missense_variant | 0.14 |
rpoB | 762684 | p.Ala960Thr | missense_variant | 0.14 |
rpoB | 762775 | p.Arg990Leu | missense_variant | 0.1 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.99 |
rpoC | 763926 | p.Ala186Asp | missense_variant | 0.15 |
rpoC | 766967 | p.Pro1200Thr | missense_variant | 0.14 |
rpoC | 766970 | p.Ala1201Thr | missense_variant | 0.27 |
rpoC | 766976 | p.Gly1203Cys | missense_variant | 0.29 |
rpoC | 766979 | p.Arg1204Cys | missense_variant | 0.12 |
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 | 777362 | p.Met373Ile | missense_variant | 0.15 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303122 | c.192G>T | synonymous_variant | 0.19 |
fbiC | 1304457 | c.1527C>T | synonymous_variant | 0.23 |
fbiC | 1305450 | c.2520C>A | synonymous_variant | 0.11 |
fbiC | 1305452 | p.Gly841Asp | missense_variant | 0.11 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407165 | p.Thr59Lys | missense_variant | 0.1 |
embR | 1416974 | p.Ala125Val | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674822 | c.621C>A | synonymous_variant | 0.12 |
rpsA | 1833410 | c.-132G>A | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834865 | p.Gly442Arg | missense_variant | 0.11 |
rpsA | 1834870 | c.1329C>A | synonymous_variant | 0.17 |
tlyA | 1917964 | p.Ala9Thr | missense_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.83 |
tlyA | 1918198 | p.Leu87Met | missense_variant | 0.12 |
tlyA | 1918570 | p.Val211Ile | missense_variant | 0.12 |
tlyA | 1918580 | p.Arg214Leu | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155743 | c.369G>T | synonymous_variant | 0.13 |
katG | 2155760 | p.Gly118Ser | missense_variant | 0.21 |
katG | 2155763 | p.Asp117Asn | missense_variant | 0.11 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170097 | c.516G>A | synonymous_variant | 0.25 |
PPE35 | 2170100 | c.513G>A | synonymous_variant | 0.18 |
PPE35 | 2170354 | p.Ala87Ser | missense_variant | 0.13 |
PPE35 | 2170357 | p.Ala86Ser | missense_variant | 0.22 |
PPE35 | 2170520 | p.Trp31* | stop_gained | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519008 | c.894C>A | synonymous_variant | 0.17 |
kasA | 2519159 | p.Ala349Ser | missense_variant | 0.12 |
eis | 2714865 | c.468C>T | synonymous_variant | 0.12 |
eis | 2714868 | c.465C>A | synonymous_variant | 0.12 |
eis | 2715037 | p.Ala99Val | missense_variant | 0.12 |
eis | 2715042 | c.291G>A | synonymous_variant | 0.19 |
folC | 2746309 | c.1290G>T | synonymous_variant | 0.11 |
folC | 2746590 | p.Gly337Cys | missense_variant | 0.11 |
pepQ | 2859603 | p.Gly272Cys | missense_variant | 0.12 |
pepQ | 2859924 | c.495G>T | synonymous_variant | 0.11 |
pepQ | 2859940 | p.Arg160His | missense_variant | 0.2 |
pepQ | 2860150 | p.Ala90Val | missense_variant | 0.12 |
pepQ | 2860182 | c.237C>T | synonymous_variant | 0.14 |
pepQ | 2860589 | c.-171G>T | upstream_gene_variant | 0.5 |
ribD | 2987306 | c.468C>A | synonymous_variant | 0.11 |
ribD | 2987307 | p.Ala157Thr | missense_variant | 0.1 |
ribD | 2987315 | c.477C>A | synonymous_variant | 0.2 |
Rv2752c | 3066291 | c.-100G>T | upstream_gene_variant | 0.14 |
Rv2752c | 3066302 | c.-111C>A | upstream_gene_variant | 0.1 |
thyX | 3067200 | p.Glu249Val | missense_variant | 0.12 |
thyX | 3067212 | p.Pro245Leu | missense_variant | 0.14 |
thyX | 3067222 | p.Ala242Ser | missense_variant | 0.5 |
thyX | 3067297 | p.Arg217Ser | missense_variant | 0.29 |
thyX | 3067298 | c.648G>A | synonymous_variant | 0.18 |
thyX | 3067302 | p.Cys215Tyr | missense_variant | 0.12 |
thyX | 3067418 | c.528C>T | synonymous_variant | 0.14 |
thyX | 3067541 | c.405C>A | synonymous_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087302 | c.483C>A | synonymous_variant | 0.11 |
ald | 3087303 | p.Gly162Arg | missense_variant | 0.14 |
ald | 3087332 | c.513C>T | synonymous_variant | 0.15 |
ald | 3087333 | p.Val172Leu | missense_variant | 0.11 |
fbiD | 3339332 | p.Ala72Glu | missense_variant | 0.11 |
fbiD | 3339558 | c.441C>A | synonymous_variant | 0.15 |
fbiD | 3339729 | c.612G>T | synonymous_variant | 0.22 |
fbiD | 3339747 | c.630G>T | synonymous_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474921 | c.915G>A | synonymous_variant | 0.12 |
fprA | 3474926 | p.Thr307Lys | missense_variant | 0.11 |
fprA | 3474983 | p.Gly326Val | missense_variant | 0.33 |
fprA | 3474989 | p.Pro328Leu | missense_variant | 0.14 |
fprA | 3475312 | p.Pro436Thr | missense_variant | 0.12 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.99 |
fbiB | 3641388 | c.-147C>T | upstream_gene_variant | 0.12 |
fbiB | 3641630 | c.96C>T | synonymous_variant | 0.1 |
fbiB | 3641907 | p.Pro125Thr | missense_variant | 0.11 |
fbiB | 3642173 | c.639G>A | synonymous_variant | 0.14 |
fbiB | 3642183 | p.Val217Met | missense_variant | 0.18 |
fbiB | 3642190 | p.Gly219Glu | missense_variant | 0.25 |
fbiB | 3642324 | p.Arg264Ser | missense_variant | 0.11 |
fbiB | 3642380 | p.Glu282Asp | missense_variant | 0.15 |
alr | 3840986 | c.435G>T | synonymous_variant | 0.12 |
alr | 3841003 | p.Glu140* | stop_gained | 0.14 |
clpC1 | 4038195 | p.Ala837Glu | missense_variant | 0.12 |
panD | 4044480 | c.-199G>T | upstream_gene_variant | 0.14 |
embC | 4242362 | p.Gly834Ser | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242687 | p.Gln942Leu | missense_variant | 0.12 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243615 | p.Arg128Leu | missense_variant | 0.18 |
embA | 4243934 | c.702C>T | synonymous_variant | 0.25 |
embA | 4244221 | p.Leu330Gln | missense_variant | 0.11 |
embA | 4244291 | c.1059G>T | synonymous_variant | 0.25 |
embA | 4244447 | c.1215G>A | synonymous_variant | 0.12 |
embA | 4244867 | c.1635C>A | synonymous_variant | 0.1 |
embA | 4244909 | c.1677C>T | synonymous_variant | 0.11 |
embA | 4245452 | c.2220G>A | synonymous_variant | 0.12 |
embA | 4245454 | p.Ala741Asp | missense_variant | 0.1 |
embA | 4245461 | c.2229C>A | synonymous_variant | 0.11 |
embB | 4246798 | c.285C>T | synonymous_variant | 0.17 |
embB | 4247108 | p.Gly199Cys | missense_variant | 0.25 |
embB | 4247645 | p.Glu378* | stop_gained | 0.18 |
embB | 4248593 | p.Gly694Ser | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267671 | p.Ala389Glu | missense_variant | 0.12 |
aftB | 4267919 | p.Gln306His | missense_variant | 0.1 |
aftB | 4267926 | p.Ala304Val | missense_variant | 0.11 |
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 |