Run ID: ERR8665609
Sample name:
Date: 02-04-2023 07:33:44
Number of reads: 323144
Percentage reads mapped: 99.5
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-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 |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288766 | p.Leu159Arg | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
embB | 4247703 | p.Pro397Gln | missense_variant | 0.38 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5081 | c.-159G>T | upstream_gene_variant | 0.2 |
gyrB | 5149 | c.-91G>T | upstream_gene_variant | 0.18 |
gyrB | 5158 | c.-82G>T | upstream_gene_variant | 0.2 |
gyrB | 5572 | c.333G>T | synonymous_variant | 0.29 |
gyrB | 5912 | p.Asp225Tyr | missense_variant | 0.29 |
gyrB | 6494 | p.Ala419Thr | missense_variant | 0.33 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7512 | p.Ala71Ser | missense_variant | 0.2 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7706 | c.405C>A | synonymous_variant | 0.33 |
gyrA | 7747 | p.Thr149Ile | missense_variant | 0.33 |
gyrA | 7751 | c.450C>A | synonymous_variant | 0.29 |
gyrA | 7982 | p.Asp227Glu | missense_variant | 0.33 |
gyrA | 8664 | p.Leu455Met | missense_variant | 0.29 |
gyrA | 9008 | p.Phe569Leu | missense_variant | 0.2 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9810 | p.Gly837Cys | missense_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575199 | c.-149G>A | upstream_gene_variant | 0.5 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576105 | p.Arg253Leu | missense_variant | 0.18 |
mshA | 576140 | p.Glu265* | stop_gained | 0.2 |
mshA | 576246 | p.Gly300Ala | missense_variant | 0.5 |
mshA | 576413 | p.Gly356Cys | missense_variant | 0.29 |
ccsA | 619953 | c.63C>A | synonymous_variant | 0.29 |
ccsA | 620316 | c.426G>T | synonymous_variant | 0.25 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620667 | p.Trp259Cys | missense_variant | 0.29 |
rpoB | 759849 | p.Pro15Thr | missense_variant | 0.19 |
rpoB | 759971 | p.Phe55Leu | missense_variant | 0.21 |
rpoB | 760229 | c.423C>A | synonymous_variant | 0.5 |
rpoB | 760977 | p.Glu391* | stop_gained | 0.33 |
rpoB | 761000 | p.Met398Ile | missense_variant | 0.29 |
rpoB | 761829 | p.Gly675Cys | missense_variant | 0.29 |
rpoB | 761891 | c.2085G>T | synonymous_variant | 0.33 |
rpoB | 762054 | p.Glu750* | stop_gained | 0.4 |
rpoB | 762215 | p.Lys803Asn | missense_variant | 0.2 |
rpoB | 762566 | p.Met920Ile | missense_variant | 0.29 |
rpoB | 762930 | p.Pro1042Thr | missense_variant | 0.14 |
rpoB | 763026 | p.Gly1074Cys | missense_variant | 0.29 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763556 | p.Gly63Cys | missense_variant | 0.25 |
rpoC | 763585 | c.216C>T | synonymous_variant | 0.4 |
rpoC | 764479 | p.Glu370Asp | missense_variant | 0.33 |
rpoC | 764817 | p.Val483Ala | missense_variant | 1.0 |
rpoC | 765262 | c.1893C>A | synonymous_variant | 0.2 |
rpoC | 766286 | p.Gly973Ser | missense_variant | 0.5 |
rpoC | 766346 | p.Glu993Lys | missense_variant | 0.25 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776045 | c.2436G>T | synonymous_variant | 0.25 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776150 | p.Met777Ile | missense_variant | 0.33 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776343 | p.Gly713Val | missense_variant | 0.2 |
mmpL5 | 777795 | p.Ser229* | stop_gained | 0.29 |
mmpL5 | 778010 | p.Gln157His | missense_variant | 0.25 |
mmpR5 | 779413 | p.Leu142Met | missense_variant | 0.25 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781716 | p.Ala53Ser | missense_variant | 0.17 |
rpsL | 781730 | p.Leu57Phe | missense_variant | 0.2 |
rplC | 800952 | c.144C>T | synonymous_variant | 0.25 |
fbiC | 1303375 | p.Asp149Tyr | missense_variant | 0.22 |
fbiC | 1304266 | c.1336C>A | synonymous_variant | 0.2 |
fbiC | 1304835 | c.1905G>T | synonymous_variant | 0.25 |
Rv1258c | 1406280 | p.Ser354* | stop_gained | 0.22 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407371 | c.-31C>A | upstream_gene_variant | 0.18 |
embR | 1416808 | c.540C>A | synonymous_variant | 0.2 |
atpE | 1461035 | c.-10G>T | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472548 | n.703A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472766 | n.921G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473515 | n.-143G>T | upstream_gene_variant | 0.21 |
rrl | 1473925 | n.268G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474063 | n.406G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474408 | n.751G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474757 | n.1100C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474928 | n.1271C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.2 |
inhA | 1673685 | c.-517C>A | upstream_gene_variant | 0.3 |
inhA | 1674939 | c.738G>T | synonymous_variant | 0.18 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.17 |
rpsA | 1833883 | c.342C>A | synonymous_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834480 | c.939C>A | synonymous_variant | 0.29 |
rpsA | 1834522 | c.981C>A | synonymous_variant | 0.25 |
rpsA | 1834598 | p.Leu353Met | missense_variant | 0.25 |
rpsA | 1834890 | p.Ser450* | stop_gained | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918686 | c.747G>T | synonymous_variant | 0.33 |
ndh | 2101746 | p.Asp433Tyr | missense_variant | 0.25 |
ndh | 2101987 | c.1056C>A | synonymous_variant | 0.25 |
ndh | 2102692 | c.351C>A | synonymous_variant | 0.33 |
katG | 2153975 | p.Ala713Thr | missense_variant | 0.33 |
katG | 2153988 | c.2124C>A | synonymous_variant | 0.4 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155166 | p.Gly316Cys | missense_variant | 0.29 |
katG | 2156050 | p.Pro21His | missense_variant | 0.33 |
katG | 2156244 | c.-133G>C | upstream_gene_variant | 0.15 |
katG | 2156283 | c.-172G>T | upstream_gene_variant | 0.4 |
katG | 2156534 | c.-423G>T | upstream_gene_variant | 0.25 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168642 | p.Phe657Leu | missense_variant | 0.23 |
PPE35 | 2169251 | c.1362C>A | synonymous_variant | 0.22 |
PPE35 | 2169804 | p.Ala270Glu | missense_variant | 0.29 |
PPE35 | 2170182 | p.Trp144Leu | missense_variant | 0.33 |
PPE35 | 2170555 | p.Gly20Cys | missense_variant | 0.22 |
Rv1979c | 2221797 | p.Phe456Leu | missense_variant | 0.42 |
Rv1979c | 2221816 | p.Ala450Asp | missense_variant | 0.15 |
Rv1979c | 2221929 | p.Phe412Leu | missense_variant | 0.22 |
Rv1979c | 2222016 | p.Phe383Leu | missense_variant | 0.29 |
Rv1979c | 2222022 | c.1143C>A | synonymous_variant | 0.29 |
Rv1979c | 2222245 | p.Gly307Val | missense_variant | 0.22 |
Rv1979c | 2222309 | p.Asp286Tyr | missense_variant | 0.18 |
Rv1979c | 2222339 | p.Leu276Met | missense_variant | 0.25 |
Rv1979c | 2222797 | p.Pro123His | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289270 | c.-29G>T | upstream_gene_variant | 0.22 |
pncA | 2290038 | c.-797G>T | upstream_gene_variant | 0.2 |
pncA | 2290062 | c.-821G>T | upstream_gene_variant | 0.22 |
kasA | 2518804 | p.Phe230Leu | missense_variant | 0.25 |
eis | 2714487 | c.846C>A | synonymous_variant | 0.29 |
eis | 2715156 | c.177C>A | synonymous_variant | 0.29 |
ahpC | 2726529 | p.Asp113Tyr | missense_variant | 0.4 |
folC | 2746636 | c.963C>A | synonymous_variant | 0.5 |
folC | 2747209 | p.Leu130Phe | missense_variant | 0.5 |
folC | 2747402 | p.Ser66* | stop_gained | 0.25 |
pepQ | 2859593 | p.Ala276Ser | missense_variant | 0.25 |
pepQ | 2859603 | p.Gly272Cys | missense_variant | 0.18 |
pepQ | 2859659 | p.Ala254Ser | missense_variant | 0.18 |
pepQ | 2859799 | p.Pro207Gln | missense_variant | 0.33 |
pepQ | 2860343 | p.Asp26Tyr | missense_variant | 0.22 |
pepQ | 2860369 | p.Ser17Tyr | missense_variant | 0.29 |
pepQ | 2860376 | p.Ala15Thr | missense_variant | 0.33 |
ribD | 2986794 | c.-45G>T | upstream_gene_variant | 0.2 |
ribD | 2986829 | c.-10A>G | upstream_gene_variant | 0.18 |
ribD | 2986911 | p.Asp25Tyr | missense_variant | 0.33 |
Rv2752c | 3065148 | c.1044C>A | synonymous_variant | 0.22 |
Rv2752c | 3065152 | p.Ala347Val | missense_variant | 0.22 |
Rv2752c | 3065228 | p.Glu322* | stop_gained | 0.43 |
Rv2752c | 3065301 | c.891C>A | synonymous_variant | 0.33 |
Rv2752c | 3065554 | p.Pro213Gln | missense_variant | 0.29 |
Rv2752c | 3065673 | p.Phe173Leu | missense_variant | 0.4 |
Rv2752c | 3065788 | p.Arg135Leu | missense_variant | 0.33 |
Rv2752c | 3066007 | p.Pro62Gln | missense_variant | 0.22 |
thyA | 3073862 | p.Gly204Cys | missense_variant | 0.25 |
thyA | 3074290 | p.Trp61Leu | missense_variant | 0.23 |
ald | 3086712 | c.-108C>A | upstream_gene_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087503 | c.684C>A | synonymous_variant | 0.25 |
ald | 3087676 | p.Pro286Arg | missense_variant | 0.12 |
fbiD | 3339382 | p.Pro89Thr | missense_variant | 0.18 |
Rv3083 | 3448476 | c.-28G>T | upstream_gene_variant | 0.25 |
Rv3083 | 3448489 | c.-15C>T | upstream_gene_variant | 0.29 |
Rv3083 | 3448731 | c.228C>A | synonymous_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474815 | p.Arg270Leu | missense_variant | 0.22 |
fprA | 3474835 | p.Glu277* | stop_gained | 0.25 |
fprA | 3475265 | p.Ser420* | stop_gained | 0.33 |
fprA | 3475313 | p.Pro436Gln | missense_variant | 0.33 |
whiB7 | 3568435 | p.Pro82Gln | missense_variant | 0.25 |
whiB7 | 3568463 | p.Gln73Lys | missense_variant | 0.22 |
whiB7 | 3568650 | c.30C>G | synonymous_variant | 0.33 |
whiB7 | 3568777 | c.-98C>A | upstream_gene_variant | 0.29 |
Rv3236c | 3611965 | c.1152G>T | synonymous_variant | 0.25 |
Rv3236c | 3612370 | c.747C>A | synonymous_variant | 0.25 |
Rv3236c | 3612550 | c.567C>T | synonymous_variant | 0.25 |
Rv3236c | 3612575 | p.Ala181Glu | missense_variant | 0.22 |
Rv3236c | 3612634 | c.483G>T | synonymous_variant | 0.25 |
Rv3236c | 3612646 | c.471C>A | synonymous_variant | 0.4 |
Rv3236c | 3612880 | c.237G>T | synonymous_variant | 0.67 |
fbiB | 3640887 | c.-648C>A | upstream_gene_variant | 0.22 |
alr | 3840340 | p.Asp361Asn | missense_variant | 0.22 |
alr | 3840383 | p.Phe346Leu | missense_variant | 0.29 |
alr | 3840763 | p.Ala220Ser | missense_variant | 0.67 |
rpoA | 3877532 | p.Ala326Thr | missense_variant | 0.25 |
rpoA | 3877533 | c.975C>A | synonymous_variant | 0.25 |
rpoA | 3878352 | c.156C>A | synonymous_variant | 0.2 |
rpoA | 3878355 | c.153C>A | synonymous_variant | 0.2 |
ddn | 3987260 | p.Trp139Cys | missense_variant | 0.18 |
clpC1 | 4038883 | p.Gly608Cys | missense_variant | 0.18 |
clpC1 | 4039025 | c.1680C>A | synonymous_variant | 0.2 |
clpC1 | 4039660 | p.Glu349* | stop_gained | 0.2 |
clpC1 | 4039690 | p.Glu339* | stop_gained | 0.22 |
clpC1 | 4039907 | p.Glu266Asp | missense_variant | 0.2 |
clpC1 | 4040746 | c.-42C>A | upstream_gene_variant | 0.25 |
panD | 4044065 | p.Gly73Cys | missense_variant | 0.2 |
panD | 4044089 | p.Gly65Cys | missense_variant | 0.22 |
embC | 4239899 | c.37C>A | synonymous_variant | 0.18 |
embC | 4240665 | p.Trp268Leu | missense_variant | 0.25 |
embC | 4240739 | p.Asp293Tyr | missense_variant | 0.4 |
embC | 4241709 | p.Arg616Leu | missense_variant | 0.33 |
embC | 4241981 | p.Pro707Thr | missense_variant | 0.22 |
embC | 4242426 | p.Arg855Leu | missense_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242816 | p.Trp985Leu | missense_variant | 0.25 |
embA | 4243238 | c.6C>A | synonymous_variant | 0.5 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243589 | c.357C>A | synonymous_variant | 0.5 |
embA | 4244124 | p.Gly298Cys | missense_variant | 0.29 |
embA | 4244239 | p.Trp336* | stop_gained | 0.29 |
embA | 4244672 | c.1440C>A | synonymous_variant | 0.29 |
embA | 4245029 | p.Ser599Arg | missense_variant | 0.17 |
embB | 4245794 | c.-720G>T | upstream_gene_variant | 0.33 |
embA | 4245962 | p.Gln910His | missense_variant | 0.67 |
embA | 4246065 | p.Asp945Tyr | missense_variant | 0.25 |
embA | 4246146 | p.Gly972Trp | missense_variant | 0.33 |
embA | 4246204 | p.Arg991Leu | missense_variant | 0.33 |
embB | 4247633 | p.Gly374Arg | missense_variant | 0.29 |
embB | 4247688 | p.Leu392Pro | missense_variant | 0.22 |
embB | 4249560 | p.Pro1016Gln | missense_variant | 0.2 |
embB | 4249796 | c.3283C>A | synonymous_variant | 0.4 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267735 | p.Gly368Cys | missense_variant | 0.22 |
aftB | 4268164 | p.Gln225* | stop_gained | 0.25 |
ubiA | 4269224 | p.Ala204Ser | missense_variant | 0.22 |
aftB | 4269228 | c.-392C>T | upstream_gene_variant | 0.22 |
ubiA | 4269294 | p.Met180Ile | missense_variant | 0.5 |
ethA | 4326141 | p.Glu445* | stop_gained | 0.4 |
ethA | 4326593 | p.Cys294Phe | missense_variant | 1.0 |
ethR | 4327781 | p.Arg78Gln | missense_variant | 0.22 |
ethR | 4328134 | p.Glu196* | stop_gained | 0.29 |
whiB6 | 4338175 | p.Ala116Val | missense_variant | 0.29 |
whiB6 | 4338450 | c.72C>A | synonymous_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338621 | c.-100G>T | upstream_gene_variant | 0.18 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407701 | p.His168Asn | missense_variant | 0.25 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4407970 | p.Pro78Gln | missense_variant | 0.18 |
gid | 4408089 | c.114C>A | synonymous_variant | 0.25 |
gid | 4408124 | p.Ala27Ser | missense_variant | 0.22 |