Run ID: ERR8665607
Sample name:
Date: 02-04-2023 07:33:45
Number of reads: 328105
Percentage reads mapped: 99.53
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761108 | p.Met434Ile | missense_variant | 0.29 | rifampicin |
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5301 | p.Glu21Gly | missense_variant | 0.1 |
gyrB | 6545 | p.Gly436Cys | missense_variant | 0.33 |
gyrB | 6650 | p.Arg471Ser | missense_variant | 0.5 |
gyrB | 6851 | p.Gln538Lys | missense_variant | 0.29 |
gyrB | 7097 | p.Glu620* | stop_gained | 0.22 |
gyrA | 7321 | p.Pro7Gln | missense_variant | 0.2 |
gyrA | 7324 | p.Pro8His | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7469 | c.168C>A | synonymous_variant | 0.25 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7624 | p.Pro108Gln | missense_variant | 0.18 |
gyrA | 7651 | p.Gly117Asp | missense_variant | 0.14 |
gyrA | 8450 | p.Lys383Asn | missense_variant | 0.18 |
gyrA | 8472 | p.Leu391Met | missense_variant | 0.2 |
gyrA | 8526 | c.1225C>A | synonymous_variant | 0.22 |
gyrA | 8578 | p.Asp426Val | missense_variant | 0.15 |
gyrA | 9222 | p.Asp641Tyr | missense_variant | 0.33 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9567 | p.Asp756Tyr | missense_variant | 0.25 |
gyrA | 9632 | c.2331C>A | synonymous_variant | 0.2 |
fgd1 | 490584 | c.-199C>A | upstream_gene_variant | 0.22 |
fgd1 | 490592 | c.-191C>A | upstream_gene_variant | 0.29 |
fgd1 | 490670 | c.-113G>T | upstream_gene_variant | 0.25 |
fgd1 | 491157 | p.Phe125Leu | missense_variant | 0.22 |
fgd1 | 491311 | p.Gly177Cys | missense_variant | 0.5 |
fgd1 | 491321 | p.Ala180Val | missense_variant | 0.5 |
fgd1 | 491580 | c.798C>A | synonymous_variant | 0.29 |
fgd1 | 491652 | c.870C>A | synonymous_variant | 0.25 |
fgd1 | 491685 | c.903G>T | synonymous_variant | 0.67 |
mshA | 575588 | p.Arg81Ser | missense_variant | 0.33 |
mshA | 575591 | c.244C>A | synonymous_variant | 0.22 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576322 | c.975G>T | synonymous_variant | 0.5 |
ccsA | 620026 | p.Pro46Thr | missense_variant | 0.5 |
ccsA | 620118 | c.228C>A | synonymous_variant | 0.5 |
ccsA | 620167 | p.Ala93Ser | missense_variant | 0.67 |
ccsA | 620171 | p.Cys94Tyr | missense_variant | 0.67 |
ccsA | 620384 | p.Pro165Gln | missense_variant | 0.22 |
ccsA | 620396 | p.Ser169Tyr | missense_variant | 0.2 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759662 | c.-145C>T | upstream_gene_variant | 0.22 |
rpoB | 760124 | p.Phe106Leu | missense_variant | 0.4 |
rpoB | 760301 | c.495C>A | synonymous_variant | 0.2 |
rpoB | 760400 | c.594G>T | synonymous_variant | 0.33 |
rpoB | 761573 | c.1767C>A | synonymous_variant | 0.33 |
rpoB | 761598 | p.Arg598Ser | missense_variant | 0.22 |
rpoB | 762651 | p.Trp949Arg | missense_variant | 0.29 |
rpoC | 762680 | c.-690C>A | upstream_gene_variant | 0.25 |
rpoC | 762794 | c.-576C>A | upstream_gene_variant | 0.29 |
rpoB | 763001 | p.Met1065Ile | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763116 | p.Glu1104* | stop_gained | 0.27 |
rpoC | 763637 | p.Glu90* | stop_gained | 0.29 |
rpoC | 763646 | p.Gly93Cys | missense_variant | 0.29 |
rpoC | 763834 | p.Met155Ile | missense_variant | 0.33 |
rpoC | 764449 | c.1080G>T | synonymous_variant | 0.4 |
rpoC | 764579 | p.Asp404Tyr | missense_variant | 0.22 |
rpoC | 764669 | p.Pro434Thr | missense_variant | 0.22 |
rpoC | 764770 | p.Gln467His | missense_variant | 0.18 |
rpoC | 764817 | p.Val483Ala | missense_variant | 1.0 |
rpoC | 764965 | p.Phe532Leu | missense_variant | 0.22 |
rpoC | 765343 | c.1974G>T | synonymous_variant | 0.4 |
rpoC | 765808 | p.Gln813His | missense_variant | 0.4 |
rpoC | 766199 | c.2830C>T | synonymous_variant | 0.2 |
rpoC | 766223 | p.Leu952Met | missense_variant | 0.25 |
rpoC | 766260 | p.Ser964* | stop_gained | 0.25 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 766744 | p.Gln1125His | missense_variant | 0.2 |
rpoC | 766982 | p.Pro1205Thr | missense_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776162 | c.2319C>A | synonymous_variant | 0.2 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776552 | p.Gln643His | missense_variant | 0.33 |
mmpL5 | 777260 | c.1221C>A | synonymous_variant | 0.29 |
mmpL5 | 777876 | p.Arg202Leu | missense_variant | 0.22 |
mmpL5 | 778621 | c.-141G>T | upstream_gene_variant | 0.33 |
mmpR5 | 779023 | p.Ala12Tyr | missense_variant | 0.22 |
mmpR5 | 779315 | p.Arg109Leu | missense_variant | 0.29 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781501 | c.-59C>A | upstream_gene_variant | 0.6 |
rpsL | 781651 | p.Arg31His | missense_variant | 0.25 |
rplC | 801219 | c.411C>A | synonymous_variant | 0.4 |
rplC | 801416 | p.Gly203Val | missense_variant | 0.17 |
rplC | 801444 | c.636C>A | synonymous_variant | 0.22 |
fbiC | 1302958 | p.Thr10Ser | missense_variant | 0.22 |
fbiC | 1303237 | p.His103Asp | missense_variant | 0.14 |
fbiC | 1304578 | p.Arg550Ser | missense_variant | 0.4 |
fbiC | 1304592 | p.Phe554Leu | missense_variant | 0.29 |
fbiC | 1305080 | p.Arg717Leu | missense_variant | 0.25 |
Rv1258c | 1406677 | p.Leu222Met | missense_variant | 0.33 |
Rv1258c | 1406722 | p.Gly207Trp | missense_variant | 0.25 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1417099 | c.249C>T | synonymous_variant | 0.25 |
embR | 1417160 | p.Trp63Leu | missense_variant | 0.2 |
embR | 1417257 | p.Gly31Cys | missense_variant | 0.29 |
embR | 1417439 | c.-92G>T | upstream_gene_variant | 0.2 |
atpE | 1461249 | p.Ala69Ser | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472343 | n.498C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472976 | n.1131G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474648 | n.991G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475034 | n.1377G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475047 | n.1390G>T | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673272 | c.-168C>T | upstream_gene_variant | 0.17 |
fabG1 | 1673436 | c.-4C>A | upstream_gene_variant | 0.33 |
inhA | 1674260 | p.Ser20* | stop_gained | 0.25 |
inhA | 1674957 | c.756G>T | synonymous_variant | 0.22 |
rpsA | 1833447 | c.-95C>A | upstream_gene_variant | 0.2 |
rpsA | 1834029 | p.Pro163His | missense_variant | 0.18 |
rpsA | 1834036 | c.495C>A | synonymous_variant | 0.27 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834519 | c.978G>T | synonymous_variant | 0.22 |
rpsA | 1834542 | p.Pro334His | missense_variant | 0.33 |
rpsA | 1834544 | p.Asp335Tyr | missense_variant | 0.22 |
rpsA | 1834752 | p.Leu404Pro | missense_variant | 0.33 |
tlyA | 1917923 | c.-17G>T | upstream_gene_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101810 | c.1233C>A | synonymous_variant | 0.2 |
ndh | 2101816 | c.1227C>A | synonymous_variant | 0.36 |
ndh | 2101846 | c.1197G>A | synonymous_variant | 0.2 |
ndh | 2101867 | c.1176C>A | synonymous_variant | 0.22 |
katG | 2154278 | p.Asp612Tyr | missense_variant | 0.27 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155663 | p.Pro150Gln | missense_variant | 0.5 |
katG | 2155957 | p.Pro52Gln | missense_variant | 0.18 |
katG | 2156256 | c.-145C>A | upstream_gene_variant | 0.29 |
katG | 2156341 | c.-230G>T | upstream_gene_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168240 | c.2373C>A | synonymous_variant | 0.25 |
PPE35 | 2169146 | c.1467G>T | synonymous_variant | 0.2 |
PPE35 | 2169283 | p.Arg444Ser | missense_variant | 0.22 |
Rv1979c | 2222695 | p.Arg157Leu | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289378 | c.-137G>T | upstream_gene_variant | 0.23 |
kasA | 2518418 | p.Glu102* | stop_gained | 0.29 |
kasA | 2518541 | p.Gln143Lys | missense_variant | 0.25 |
kasA | 2518549 | c.435C>A | synonymous_variant | 0.2 |
kasA | 2518564 | c.450C>A | synonymous_variant | 0.22 |
kasA | 2519308 | c.1194C>A | synonymous_variant | 0.2 |
ahpC | 2726232 | p.Gln14Lys | missense_variant | 0.23 |
ahpC | 2726513 | c.321C>A | synonymous_variant | 0.18 |
folC | 2746376 | p.Ser408* | stop_gained | 0.29 |
folC | 2747026 | c.573C>A | synonymous_variant | 0.25 |
folC | 2747103 | p.Ala166Ser | missense_variant | 0.17 |
folC | 2747273 | p.Ser109* | stop_gained | 0.22 |
folC | 2747287 | c.312G>T | synonymous_variant | 0.22 |
folC | 2747344 | c.255G>T | synonymous_variant | 0.25 |
pepQ | 2859599 | p.Asp274Tyr | missense_variant | 0.67 |
pepQ | 2859722 | p.Met233Val | missense_variant | 0.33 |
pepQ | 2860484 | c.-66G>T | upstream_gene_variant | 0.29 |
ribD | 2987138 | c.300C>A | synonymous_variant | 0.5 |
ribD | 2987285 | c.447C>A | synonymous_variant | 0.22 |
thyX | 3067590 | p.Pro119Gln | missense_variant | 0.29 |
thyX | 3067823 | c.123G>T | synonymous_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087758 | c.939G>T | synonymous_variant | 0.29 |
Rv3083 | 3449324 | p.Arg274Leu | missense_variant | 0.25 |
fprA | 3473836 | c.-171C>A | upstream_gene_variant | 0.38 |
fprA | 3473874 | c.-133C>A | upstream_gene_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474492 | c.486G>T | synonymous_variant | 0.18 |
fprA | 3475140 | c.1134C>A | synonymous_variant | 0.22 |
fprA | 3475294 | p.Glu430* | stop_gained | 0.4 |
whiB7 | 3568478 | p.Gly68Cys | missense_variant | 0.22 |
Rv3236c | 3612025 | c.1092C>A | synonymous_variant | 0.29 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641537 | c.3G>T | start_lost | 0.67 |
fbiB | 3641736 | p.Glu68* | stop_gained | 0.25 |
fbiB | 3641749 | p.Arg72Leu | missense_variant | 0.25 |
fbiB | 3641753 | p.Leu73Phe | missense_variant | 0.29 |
fbiB | 3642362 | c.828C>A | synonymous_variant | 0.33 |
fbiB | 3642470 | c.936G>T | synonymous_variant | 0.25 |
fbiB | 3642484 | p.Trp317Leu | missense_variant | 0.29 |
alr | 3840316 | p.Gly369Cys | missense_variant | 0.25 |
alr | 3840464 | p.Phe319Leu | missense_variant | 0.5 |
alr | 3840619 | p.Asp268Tyr | missense_variant | 0.29 |
alr | 3840646 | p.Gly259Trp | missense_variant | 0.2 |
rpoA | 3877691 | p.Gly273Cys | missense_variant | 0.33 |
rpoA | 3878582 | c.-75C>A | upstream_gene_variant | 0.25 |
ddn | 3987235 | p.Pro131Gln | missense_variant | 0.22 |
clpC1 | 4039475 | p.Met410Ile | missense_variant | 0.22 |
clpC1 | 4040549 | p.Leu52Phe | missense_variant | 0.2 |
embC | 4241274 | p.Pro471Gln | missense_variant | 0.29 |
embC | 4241318 | p.Pro486Thr | missense_variant | 0.25 |
embC | 4241330 | p.Asp490Tyr | missense_variant | 0.25 |
embC | 4241581 | c.1719C>A | synonymous_variant | 0.22 |
embC | 4242034 | c.2172C>A | synonymous_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243451 | c.219G>T | synonymous_variant | 0.29 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243763 | c.531G>T | synonymous_variant | 0.67 |
embA | 4243766 | p.Lys178Asn | missense_variant | 0.67 |
embA | 4244669 | c.1437G>T | synonymous_variant | 0.2 |
embA | 4245086 | c.1854C>A | synonymous_variant | 0.17 |
embA | 4245308 | c.2076G>T | synonymous_variant | 0.25 |
embA | 4245724 | p.Gly831Val | missense_variant | 0.22 |
embA | 4246153 | p.Ala974Val | missense_variant | 0.25 |
embB | 4246352 | c.-162G>T | upstream_gene_variant | 0.25 |
embA | 4246394 | p.Trp1054Cys | missense_variant | 0.2 |
embB | 4246403 | c.-111G>T | upstream_gene_variant | 0.18 |
embA | 4246417 | p.Arg1062Leu | missense_variant | 0.2 |
embB | 4246587 | p.Gly25Val | missense_variant | 0.29 |
embB | 4247215 | c.702C>A | synonymous_variant | 0.33 |
embB | 4247707 | p.Phe398Leu | missense_variant | 0.33 |
embB | 4248012 | p.Ser500* | stop_gained | 0.22 |
embB | 4248041 | p.Ala510Ser | missense_variant | 0.25 |
embB | 4248050 | p.Gly513Trp | missense_variant | 0.25 |
embB | 4248723 | p.Trp737Leu | missense_variant | 0.22 |
embB | 4248745 | c.2232C>T | synonymous_variant | 0.22 |
embB | 4248775 | c.2262C>A | synonymous_variant | 0.22 |
aftB | 4267131 | p.Pro569Arg | missense_variant | 0.17 |
aftB | 4267216 | p.Gly541* | stop_gained | 0.22 |
aftB | 4267219 | p.Asp540Tyr | missense_variant | 0.22 |
aftB | 4267238 | p.Phe533Leu | missense_variant | 0.33 |
aftB | 4267373 | c.1463delT | frameshift_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268610 | p.Pro76Gln | missense_variant | 0.22 |
aftB | 4268707 | p.Gly44Cys | missense_variant | 0.33 |
ethA | 4326383 | p.Thr364Asn | missense_variant | 0.15 |
ethA | 4326498 | p.Arg326Trp | missense_variant | 0.18 |
ethA | 4326503 | p.Gly324Val | missense_variant | 0.18 |
ethA | 4326593 | p.Cys294Phe | missense_variant | 1.0 |
ethR | 4326901 | c.-648C>A | upstream_gene_variant | 0.22 |
ethA | 4327471 | c.3G>T | start_lost | 0.2 |
ethR | 4327777 | p.Asp77Tyr | missense_variant | 0.2 |
ethR | 4327780 | p.Arg78Trp | missense_variant | 0.22 |
ethA | 4328133 | c.-660C>A | upstream_gene_variant | 0.18 |
ethA | 4328212 | c.-739G>T | upstream_gene_variant | 0.2 |
ethA | 4328226 | c.-753G>T | upstream_gene_variant | 0.22 |
ethA | 4328245 | c.-772C>A | upstream_gene_variant | 0.18 |
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 |
gid | 4408013 | c.190C>A | synonymous_variant | 0.18 |
gid | 4408093 | p.Gly37Val | missense_variant | 0.2 |
gid | 4408117 | p.Pro29His | missense_variant | 0.18 |
gid | 4408195 | p.Pro3Leu | missense_variant | 0.25 |
gid | 4408343 | c.-141C>A | upstream_gene_variant | 0.25 |