Run ID: SRR21277805
Sample name:
Date: 04-04-2023 01:44:09
Number of reads: 14188688
Percentage reads mapped: 98.24
Strain: lineage2.2.1.1
Drug-resistance: Other
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 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7572 | p.Ser91Pro | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
embB | 4247850 | p.Pro446His | missense_variant | 0.5 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7460 | c.159C>A | synonymous_variant | 0.14 |
gyrA | 7541 | c.240C>A | synonymous_variant | 0.1 |
gyrA | 7549 | p.Asn83Ile | missense_variant | 0.1 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7619 | c.318C>A | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9312 | p.Leu671Met | missense_variant | 0.12 |
fgd1 | 490682 | c.-101C>A | upstream_gene_variant | 0.33 |
fgd1 | 490694 | c.-89G>T | upstream_gene_variant | 0.16 |
fgd1 | 491311 | p.Gly177Ser | missense_variant | 0.19 |
fgd1 | 491347 | p.Gly189Cys | missense_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575287 | c.-61A>T | upstream_gene_variant | 0.12 |
mshA | 575534 | p.Gly63Cys | missense_variant | 0.11 |
mshA | 575655 | p.Val103Glu | missense_variant | 0.1 |
mshA | 575661 | p.Pro105His | missense_variant | 0.12 |
mshA | 575663 | p.Gly106Arg | missense_variant | 0.11 |
mshA | 575892 | p.Ala182Val | missense_variant | 0.22 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575919 | p.Gly191Val | missense_variant | 0.14 |
mshA | 576254 | p.Gly303Cys | missense_variant | 0.23 |
mshA | 576450 | p.Pro368Gln | missense_variant | 0.4 |
mshA | 576709 | c.1362C>A | synonymous_variant | 0.5 |
mshA | 576742 | c.1395G>T | synonymous_variant | 0.33 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.14 |
ccsA | 619818 | c.-73G>T | upstream_gene_variant | 0.14 |
ccsA | 619924 | p.Arg12Ser | missense_variant | 0.16 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760453 | p.Val216Asp | missense_variant | 0.12 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.14 |
rpoB | 761210 | c.1404C>T | synonymous_variant | 0.14 |
rpoB | 761458 | p.Pro551Gln | missense_variant | 0.11 |
rpoB | 761658 | p.Pro618Lys | missense_variant | 0.12 |
rpoB | 761691 | p.Ala629Ser | missense_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763969 | c.600C>T | synonymous_variant | 0.15 |
rpoC | 763971 | p.Gly201Val | missense_variant | 0.11 |
rpoC | 764547 | p.Gly393Glu | missense_variant | 0.15 |
rpoC | 764551 | c.1182G>A | synonymous_variant | 0.15 |
rpoC | 764560 | c.1191T>A | synonymous_variant | 0.4 |
rpoC | 765278 | p.Leu637Met | missense_variant | 0.11 |
rpoC | 765282 | p.Thr638Asn | missense_variant | 0.15 |
rpoC | 766136 | p.Arg923Trp | missense_variant | 0.13 |
rpoC | 766482 | p.Arg1038Gln | missense_variant | 0.12 |
rpoC | 766967 | p.Pro1200Thr | missense_variant | 0.17 |
rpoC | 766993 | p.Met1208Ile | missense_variant | 0.11 |
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 | 777283 | c.1198C>T | synonymous_variant | 0.1 |
mmpL5 | 777393 | p.Arg363Gln | missense_variant | 0.1 |
mmpL5 | 779352 | c.-872C>T | upstream_gene_variant | 0.11 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801234 | c.426G>A | synonymous_variant | 0.2 |
fbiC | 1303093 | p.Leu55Ile | missense_variant | 0.13 |
fbiC | 1303098 | c.168C>A | synonymous_variant | 0.27 |
fbiC | 1303134 | c.204G>T | synonymous_variant | 0.15 |
fbiC | 1303135 | p.Gly69Cys | missense_variant | 0.11 |
fbiC | 1304432 | p.Ser501* | stop_gained | 0.12 |
fbiC | 1304478 | c.1548G>T | synonymous_variant | 0.11 |
fbiC | 1305459 | c.2529G>A | synonymous_variant | 1.0 |
Rv1258c | 1406170 | p.Gly391Arg | missense_variant | 0.12 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.98 |
Rv1258c | 1406988 | p.Pro118Leu | missense_variant | 0.25 |
Rv1258c | 1407515 | c.-175G>T | upstream_gene_variant | 0.12 |
Rv1258c | 1407517 | c.-177G>T | upstream_gene_variant | 0.18 |
Rv1258c | 1407519 | c.-179C>T | upstream_gene_variant | 0.33 |
embR | 1416473 | p.Leu292Gln | missense_variant | 0.18 |
embR | 1416962 | p.Gly129Phe | missense_variant | 0.1 |
embR | 1416974 | p.Ala125Glu | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674430 | p.Arg77Trp | missense_variant | 0.13 |
inhA | 1674822 | c.621C>A | synonymous_variant | 0.13 |
inhA | 1674857 | p.Glu219Val | missense_variant | 0.13 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834862 | p.Ala441Thr | missense_variant | 0.12 |
rpsA | 1834920 | p.Ala460Val | missense_variant | 0.11 |
tlyA | 1917955 | p.Arg6Ser | missense_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918072 | p.Ala45Ser | missense_variant | 0.4 |
tlyA | 1918323 | c.384G>T | synonymous_variant | 0.21 |
tlyA | 1918333 | p.Glu132* | stop_gained | 0.17 |
tlyA | 1918555 | c.616C>A | synonymous_variant | 0.11 |
tlyA | 1918584 | c.645A>T | synonymous_variant | 0.38 |
tlyA | 1918610 | p.Gly224Val | missense_variant | 0.1 |
ndh | 2101684 | p.Gln453Tyr | missense_variant | 0.14 |
ndh | 2101699 | c.1344G>A | synonymous_variant | 0.12 |
ndh | 2102200 | c.843G>T | synonymous_variant | 0.18 |
ndh | 2102208 | p.Gly279Trp | missense_variant | 0.14 |
ndh | 2102230 | c.813G>A | synonymous_variant | 0.11 |
ndh | 2102374 | c.669G>A | synonymous_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155737 | p.Gly125Val | missense_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170025 | c.588G>T | synonymous_variant | 0.12 |
PPE35 | 2170032 | p.Gly194Val | missense_variant | 0.4 |
PPE35 | 2170349 | c.264C>T | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518593 | p.Ala160Asp | missense_variant | 0.15 |
kasA | 2518725 | p.Ala204Val | missense_variant | 0.13 |
kasA | 2518871 | p.His253Tyr | missense_variant | 1.0 |
kasA | 2519179 | c.1065G>T | synonymous_variant | 0.22 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
eis | 2714903 | c.430C>A | synonymous_variant | 0.25 |
eis | 2715025 | p.Glu103Val | missense_variant | 0.33 |
eis | 2715057 | p.Arg92Gln | missense_variant | 0.33 |
eis | 2715562 | c.-230G>T | upstream_gene_variant | 0.15 |
eis | 2715565 | c.-233C>T | upstream_gene_variant | 0.22 |
folC | 2746255 | c.1344C>T | synonymous_variant | 0.1 |
folC | 2746374 | p.Pro409Thr | missense_variant | 0.2 |
folC | 2746376 | p.Ser408* | stop_gained | 0.11 |
folC | 2746570 | c.1029C>T | synonymous_variant | 0.11 |
folC | 2746635 | p.Asp322Asn | missense_variant | 0.14 |
folC | 2746636 | c.963C>A | synonymous_variant | 0.11 |
folC | 2746827 | p.Arg258Trp | missense_variant | 0.1 |
folC | 2747119 | p.Phe160Leu | missense_variant | 0.12 |
folC | 2747344 | c.255G>A | synonymous_variant | 0.14 |
folC | 2747348 | p.Ala84Glu | missense_variant | 0.14 |
folC | 2747772 | c.-174C>T | upstream_gene_variant | 0.29 |
pepQ | 2859588 | c.831G>T | synonymous_variant | 0.1 |
pepQ | 2859596 | p.Ala275Ser | missense_variant | 0.14 |
pepQ | 2859623 | p.Pro266Thr | missense_variant | 0.17 |
pepQ | 2859954 | c.465C>A | synonymous_variant | 0.38 |
pepQ | 2859959 | p.Leu154Met | missense_variant | 0.15 |
pepQ | 2859965 | p.Ala152Thr | missense_variant | 0.17 |
pepQ | 2860583 | c.-165G>T | upstream_gene_variant | 0.13 |
pepQ | 2860585 | c.-167G>T | upstream_gene_variant | 0.11 |
pepQ | 2860589 | c.-171G>A | upstream_gene_variant | 0.75 |
ribD | 2987298 | p.Gln154Lys | missense_variant | 0.11 |
ribD | 2987378 | c.540C>T | synonymous_variant | 0.14 |
Rv2752c | 3066294 | c.-103C>T | upstream_gene_variant | 0.14 |
Rv2752c | 3066323 | c.-132G>A | upstream_gene_variant | 0.11 |
Rv2752c | 3066326 | c.-135C>A | upstream_gene_variant | 0.12 |
Rv2752c | 3067011 | c.-820C>T | upstream_gene_variant | 0.17 |
Rv2752c | 3067031 | c.-840G>A | upstream_gene_variant | 0.17 |
Rv2752c | 3067042 | c.-851C>A | upstream_gene_variant | 0.19 |
Rv2752c | 3067081 | c.-890T>A | upstream_gene_variant | 0.1 |
thyX | 3067851 | p.Gly32Val | missense_variant | 0.11 |
thyX | 3067993 | c.-48C>A | upstream_gene_variant | 0.67 |
thyA | 3074520 | c.-49G>T | upstream_gene_variant | 0.12 |
thyA | 3074523 | c.-52G>A | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087326 | c.507C>T | synonymous_variant | 0.25 |
ald | 3087345 | p.Ala176Ser | missense_variant | 0.1 |
fbiD | 3339048 | c.-70C>T | upstream_gene_variant | 0.12 |
fbiD | 3339308 | p.Pro64Gln | missense_variant | 0.14 |
fbiD | 3339319 | p.Ala68Thr | missense_variant | 0.18 |
fbiD | 3339339 | c.222G>T | synonymous_variant | 0.21 |
fbiD | 3339549 | c.432T>A | synonymous_variant | 0.11 |
fbiD | 3339554 | p.Thr146Asn | missense_variant | 0.11 |
fbiD | 3339556 | p.Gly147Ser | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474922 | p.Asp306Asn | missense_variant | 0.13 |
Rv3236c | 3612137 | p.Gly327Val | missense_variant | 0.12 |
Rv3236c | 3612171 | p.Glu316* | stop_gained | 0.15 |
Rv3236c | 3612177 | c.940C>A | synonymous_variant | 0.11 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.97 |
fbiB | 3640767 | c.-768C>T | upstream_gene_variant | 0.1 |
fbiA | 3641222 | p.Pro227His | missense_variant | 0.12 |
fbiB | 3641633 | c.99C>A | synonymous_variant | 0.14 |
fbiB | 3642392 | c.858G>T | synonymous_variant | 0.17 |
fbiB | 3642394 | p.Pro287Leu | missense_variant | 0.12 |
fbiB | 3642411 | p.Arg293Trp | missense_variant | 0.11 |
fbiB | 3642660 | p.Ala376Thr | missense_variant | 0.11 |
fbiB | 3642663 | p.Val377Ile | missense_variant | 0.13 |
alr | 3840966 | p.Ala152Val | missense_variant | 0.11 |
alr | 3841226 | c.195C>A | synonymous_variant | 0.14 |
clpC1 | 4038186 | p.Ala840Val | missense_variant | 0.14 |
clpC1 | 4038222 | p.Ala828Asp | missense_variant | 0.1 |
clpC1 | 4040226 | p.Gly160Val | missense_variant | 0.11 |
panD | 4044470 | c.-189C>T | upstream_gene_variant | 0.11 |
panD | 4044478 | c.-197G>T | upstream_gene_variant | 0.25 |
embC | 4240572 | p.Gly237Glu | missense_variant | 0.2 |
embC | 4240641 | p.Arg260Leu | missense_variant | 0.18 |
embC | 4240643 | p.Arg261Leu | missense_variant | 0.14 |
embC | 4240999 | p.Trp379* | stop_gained | 0.1 |
embC | 4241002 | c.1140G>A | synonymous_variant | 0.14 |
embC | 4241102 | p.Glu414Lys | missense_variant | 0.13 |
embC | 4241681 | p.Ala607Thr | missense_variant | 0.27 |
embC | 4241696 | p.Ala612Ser | missense_variant | 0.13 |
embC | 4242183 | p.Ala774Val | missense_variant | 0.18 |
embC | 4242195 | p.Gly778Val | missense_variant | 0.12 |
embC | 4242323 | p.Gly821Asn | missense_variant | 0.1 |
embC | 4242336 | p.Gly825Asp | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242761 | p.Arg967Trp | missense_variant | 0.14 |
embA | 4243171 | c.-62C>T | upstream_gene_variant | 0.12 |
embA | 4243190 | c.-43G>T | upstream_gene_variant | 0.1 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243554 | p.Arg108Ser | missense_variant | 0.25 |
embA | 4243630 | p.Ala133Val | missense_variant | 0.13 |
embA | 4243634 | c.402A>T | synonymous_variant | 0.11 |
embA | 4243896 | p.Ala222Asn | missense_variant | 0.21 |
embA | 4244211 | p.Pro327Thr | missense_variant | 0.1 |
embA | 4244221 | p.Leu330Gln | missense_variant | 0.18 |
embA | 4244432 | c.1200C>A | synonymous_variant | 0.13 |
embA | 4244601 | p.Ala457Ser | missense_variant | 0.21 |
embA | 4244840 | c.1608G>A | synonymous_variant | 0.12 |
embA | 4245437 | p.Met735Ile | missense_variant | 0.16 |
embA | 4245444 | p.Asp738Asn | missense_variant | 0.12 |
embB | 4245515 | c.-999C>T | upstream_gene_variant | 0.12 |
embB | 4245821 | c.-693C>T | upstream_gene_variant | 0.13 |
embB | 4246651 | c.138G>A | synonymous_variant | 0.33 |
embB | 4246800 | p.Gly96Val | missense_variant | 0.22 |
embB | 4247022 | p.Ala170Glu | missense_variant | 0.12 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.25 |
embB | 4247128 | c.615C>T | synonymous_variant | 0.17 |
embB | 4247298 | p.Pro262Leu | missense_variant | 0.11 |
embB | 4247672 | p.Ala387Ser | missense_variant | 0.13 |
embB | 4247832 | p.Phe440Tyr | missense_variant | 0.12 |
embB | 4247916 | p.Arg468Leu | missense_variant | 0.22 |
embB | 4247921 | p.His470Tyr | missense_variant | 0.11 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
embB | 4248588 | p.Gly692Asp | missense_variant | 0.17 |
embB | 4248591 | p.Ala693Asp | missense_variant | 0.4 |
embB | 4248629 | p.Pro706Ser | missense_variant | 0.1 |
embB | 4249169 | p.Asn886His | missense_variant | 0.94 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267907 | c.930C>T | synonymous_variant | 0.12 |
aftB | 4267966 | p.Arg291Ser | missense_variant | 0.17 |
aftB | 4267982 | c.855C>A | synonymous_variant | 0.15 |
aftB | 4268468 | c.369G>T | synonymous_variant | 0.11 |
aftB | 4268475 | p.Gly121Val | missense_variant | 0.1 |
aftB | 4268485 | p.Leu118Ile | missense_variant | 0.12 |
aftB | 4268885 | c.-49C>A | upstream_gene_variant | 0.5 |
aftB | 4268896 | c.-60G>A | upstream_gene_variant | 0.12 |
ubiA | 4269716 | c.106_117delCCGCTGGCCGCG | conservative_inframe_deletion | 0.18 |
ethA | 4326891 | p.Ala195Thr | missense_variant | 0.11 |
ethA | 4327599 | c.-126G>T | upstream_gene_variant | 0.12 |
ethR | 4327600 | p.Ala18Thr | missense_variant | 0.11 |
ethA | 4328023 | c.-550G>T | upstream_gene_variant | 0.14 |
ethA | 4328028 | c.-555G>T | upstream_gene_variant | 0.15 |
ethA | 4328046 | c.-573C>A | upstream_gene_variant | 0.17 |
ethR | 4328047 | p.Pro167Ser | missense_variant | 0.12 |
ethA | 4328421 | c.-948G>T | upstream_gene_variant | 0.11 |
whiB6 | 4338194 | p.Arg110Trp | missense_variant | 0.12 |
whiB6 | 4338201 | c.321C>T | synonymous_variant | 0.11 |
whiB6 | 4338207 | c.315G>T | synonymous_variant | 0.15 |
whiB6 | 4338313 | p.Ala70Val | missense_variant | 0.5 |
whiB6 | 4338334 | p.Ala63Glu | missense_variant | 0.13 |
whiB6 | 4338345 | c.177G>A | synonymous_variant | 0.1 |
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 | 4408104 | c.99G>T | synonymous_variant | 0.1 |
gid | 4408316 | c.-114C>A | upstream_gene_variant | 0.12 |