Run ID: SRR14334195
Sample name:
Date: 03-04-2023 10:33:06
Number of reads: 1716185
Percentage reads mapped: 48.46
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrA | 7572 | p.Ser91Pro | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.86 | streptomycin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.19 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.38 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.15 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2154550 | c.1561delC | frameshift_variant | 0.15 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289207 | p.Asp12Gly | missense_variant | 1.0 | pyrazinamide |
embB | 4248003 | p.Gln497Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5726 | p.Pro163Thr | missense_variant | 0.2 |
gyrB | 5819 | p.Leu194Met | missense_variant | 0.14 |
gyrB | 5968 | c.729G>A | synonymous_variant | 0.4 |
gyrB | 6051 | p.Ile271Thr | missense_variant | 0.2 |
gyrB | 6377 | p.Val380Ile | missense_variant | 0.18 |
gyrB | 6534 | p.Ala432Asp | missense_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7426 | p.Pro42Leu | missense_variant | 0.33 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7604 | c.306dupC | frameshift_variant | 0.13 |
gyrA | 8777 | p.Asp492Glu | missense_variant | 0.22 |
gyrA | 9117 | p.Glu606Tyr | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9594 | p.Ala765Ser | missense_variant | 0.18 |
gyrA | 9641 | c.2340C>T | synonymous_variant | 0.17 |
fgd1 | 490949 | p.Ser56Tyr | missense_variant | 0.2 |
fgd1 | 491094 | c.312C>A | synonymous_variant | 0.17 |
fgd1 | 491256 | p.Lys158Asn | missense_variant | 0.2 |
fgd1 | 491369 | p.Ser196Cys | missense_variant | 0.67 |
fgd1 | 491664 | c.882C>A | synonymous_variant | 0.14 |
fgd1 | 491717 | p.Ala312Glu | missense_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575191 | c.-157C>A | upstream_gene_variant | 0.14 |
mshA | 575659 | c.315dupC | frameshift_variant | 0.29 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576307 | c.960C>T | synonymous_variant | 0.25 |
mshA | 576315 | p.Ala323Val | missense_variant | 0.2 |
mshA | 576434 | p.Gln363Glu | missense_variant | 1.0 |
mshA | 576784 | c.1437C>A | synonymous_variant | 0.33 |
ccsA | 619819 | c.-72G>A | upstream_gene_variant | 0.18 |
ccsA | 620605 | p.Val239Phe | missense_variant | 0.18 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.91 |
rpoB | 760491 | p.Thr229Ala | missense_variant | 0.2 |
rpoB | 760519 | p.Thr238Asn | missense_variant | 0.33 |
rpoB | 760760 | c.954C>T | synonymous_variant | 0.33 |
rpoB | 761012 | p.Asp402Glu | missense_variant | 0.17 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.25 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.4 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.29 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.22 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.18 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.18 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.22 |
rpoB | 761282 | c.1476C>G | synonymous_variant | 0.22 |
rpoB | 761777 | p.Asp657Glu | missense_variant | 0.2 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.18 |
rpoB | 762815 | p.Met1003Ile | missense_variant | 0.25 |
rpoC | 762842 | c.-528G>T | upstream_gene_variant | 0.25 |
rpoB | 762951 | p.Gln1049Lys | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763083 | p.Arg1093Ser | missense_variant | 1.0 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.25 |
rpoB | 763250 | p.Asp1148Glu | missense_variant | 0.13 |
rpoC | 763772 | p.Val135Leu | missense_variant | 0.22 |
rpoC | 763934 | p.Ala189Ser | missense_variant | 0.14 |
rpoC | 764229 | p.Gln287Arg | missense_variant | 0.29 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.33 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.38 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.25 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.33 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.33 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.33 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.33 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.33 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.4 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.4 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.4 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.33 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.21 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.29 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.25 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.18 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.31 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.33 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.33 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.36 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.18 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.5 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.33 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.56 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.33 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.33 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.22 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.25 |
rpoC | 764781 | p.Ser471Thr | missense_variant | 0.17 |
rpoC | 764828 | p.Leu487Ile | missense_variant | 0.14 |
rpoC | 764854 | c.1485G>T | synonymous_variant | 0.17 |
rpoC | 764916 | p.Leu516Pro | missense_variant | 0.93 |
rpoC | 765722 | p.Val785Ile | missense_variant | 0.17 |
rpoC | 765891 | p.Arg841Leu | missense_variant | 0.18 |
rpoC | 766310 | p.Arg981Ser | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775691 | c.2790G>T | synonymous_variant | 0.14 |
mmpL5 | 775875 | p.Gly869Val | missense_variant | 0.5 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776266 | p.Lys739Glu | missense_variant | 0.29 |
mmpL5 | 776380 | p.Phe701Leu | missense_variant | 0.2 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.17 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.15 |
mmpL5 | 777830 | c.651G>T | synonymous_variant | 0.15 |
mmpS5 | 778562 | p.Arg115Leu | missense_variant | 0.2 |
mmpS5 | 778731 | p.Glu59* | stop_gained | 0.2 |
mmpL5 | 779223 | c.-743C>A | upstream_gene_variant | 0.15 |
mmpR5 | 779230 | p.Glu81* | stop_gained | 0.14 |
mmpR5 | 779264 | p.Tyr92Cys | missense_variant | 0.18 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.92 |
mmpS5 | 779666 | c.-761G>T | upstream_gene_variant | 0.18 |
mmpS5 | 779682 | c.-777G>T | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801041 | p.Arg78Leu | missense_variant | 0.22 |
rplC | 801103 | p.Gln99Lys | missense_variant | 0.25 |
rplC | 801141 | p.Tyr111* | stop_gained | 0.22 |
fbiC | 1302776 | c.-155C>A | upstream_gene_variant | 0.18 |
fbiC | 1304097 | c.1167G>A | synonymous_variant | 0.29 |
Rv1258c | 1406171 | c.1170C>T | synonymous_variant | 1.0 |
Rv1258c | 1406477 | c.864C>G | synonymous_variant | 0.2 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406832 | p.Gly170Asp | missense_variant | 0.22 |
Rv1258c | 1406848 | p.Ile165Val | missense_variant | 0.25 |
Rv1258c | 1406893 | p.Leu150Phe | missense_variant | 0.17 |
Rv1258c | 1407515 | c.-175G>A | upstream_gene_variant | 0.18 |
embR | 1416573 | p.Pro259Thr | missense_variant | 0.22 |
atpE | 1461167 | c.123G>T | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472430 | n.585C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472996 | n.1151T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473062 | n.1217T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473065 | n.1220C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473226 | n.1381C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473288 | n.1443C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473363 | n.1519_1520delGC | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474549 | n.892G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474644 | n.987G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474752 | n.1096delA | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474806 | n.1149A>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475158 | n.1501C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475645 | n.1988C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.34 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476566 | n.2909A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476588 | n.2931A>G | non_coding_transcript_exon_variant | 0.21 |
inhA | 1673524 | c.-678C>T | upstream_gene_variant | 0.22 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 1.0 |
rpsA | 1833627 | p.Thr29Arg | missense_variant | 0.15 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.29 |
rpsA | 1833700 | c.159C>G | synonymous_variant | 0.29 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.33 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.29 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.22 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.22 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 0.25 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834406 | p.Arg289Ser | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102228 | p.Ala272Val | missense_variant | 0.33 |
ndh | 2102593 | c.450C>A | synonymous_variant | 0.15 |
ndh | 2103037 | c.3_5delGAG | start_lost&disruptive_inframe_deletion | 0.15 |
katG | 2153993 | p.Leu707Ile | missense_variant | 0.18 |
katG | 2154003 | p.Glu703Asp | missense_variant | 0.15 |
katG | 2154057 | c.2055C>A | synonymous_variant | 0.2 |
katG | 2154659 | p.Gly485Ser | missense_variant | 0.33 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155396 | p.Pro239Leu | missense_variant | 0.2 |
katG | 2156065 | p.Ala16Asp | missense_variant | 0.18 |
katG | 2156553 | c.-442G>C | upstream_gene_variant | 0.12 |
PPE35 | 2167919 | c.2694T>C | synonymous_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167955 | c.2658A>C | synonymous_variant | 0.18 |
PPE35 | 2168208 | p.Asp802Gly | missense_variant | 0.12 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.12 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.12 |
PPE35 | 2170280 | c.333C>G | synonymous_variant | 0.18 |
PPE35 | 2170406 | c.207A>G | synonymous_variant | 0.33 |
Rv1979c | 2222357 | p.Thr270Ala | missense_variant | 0.29 |
Rv1979c | 2222913 | c.252C>A | synonymous_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288745 | p.Asp166Gly | missense_variant | 0.17 |
pncA | 2289368 | c.-127G>T | upstream_gene_variant | 0.14 |
kasA | 2518016 | c.-99A>G | upstream_gene_variant | 0.12 |
kasA | 2518264 | c.150C>T | synonymous_variant | 0.2 |
kasA | 2518323 | p.Ser70Asn | missense_variant | 0.14 |
kasA | 2518433 | p.Arg107Trp | missense_variant | 0.22 |
kasA | 2518683 | p.Ala190Asp | missense_variant | 0.2 |
kasA | 2519053 | c.939G>C | synonymous_variant | 0.12 |
eis | 2714138 | p.Ala399Pro | missense_variant | 0.17 |
eis | 2714377 | p.Thr319Lys | missense_variant | 0.15 |
ahpC | 2726152 | c.-41C>A | upstream_gene_variant | 0.14 |
folC | 2747136 | p.Leu155Ile | missense_variant | 0.22 |
pepQ | 2859519 | c.900G>A | synonymous_variant | 0.2 |
pepQ | 2860470 | c.-52G>A | upstream_gene_variant | 0.2 |
ribD | 2986733 | c.-106C>A | upstream_gene_variant | 0.2 |
ribD | 2986852 | p.Gly5Val | missense_variant | 0.15 |
ribD | 2987361 | p.Glu175* | stop_gained | 0.18 |
Rv2752c | 3064740 | c.1452C>A | synonymous_variant | 0.18 |
Rv2752c | 3065169 | c.1023C>T | synonymous_variant | 0.29 |
Rv2752c | 3065633 | p.Gly187Arg | missense_variant | 0.33 |
thyX | 3067716 | p.Ser77Ile | missense_variant | 0.17 |
thyA | 3073905 | c.567C>T | synonymous_variant | 0.18 |
thyA | 3074096 | c.376C>A | synonymous_variant | 0.22 |
thyA | 3074116 | p.Leu119Pro | missense_variant | 0.17 |
thyA | 3074150 | p.His108Asn | missense_variant | 0.14 |
thyA | 3074412 | p.Asp20Glu | missense_variant | 0.22 |
thyA | 3074446 | p.Arg9His | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086899 | p.Thr27Asn | missense_variant | 0.14 |
ald | 3086950 | p.Ala44Gly | missense_variant | 0.18 |
ald | 3087294 | p.Leu159Met | missense_variant | 0.15 |
ald | 3087419 | p.Asn200Lys | missense_variant | 0.18 |
Rv3083 | 3448361 | c.-143G>T | upstream_gene_variant | 0.17 |
Rv3083 | 3449835 | c.1332G>T | synonymous_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474176 | p.His57Pro | missense_variant | 0.17 |
fprA | 3474428 | p.Val141Glu | missense_variant | 0.15 |
fprA | 3474585 | p.Glu193Asp | missense_variant | 0.15 |
whiB7 | 3568614 | c.66C>A | synonymous_variant | 0.18 |
whiB7 | 3568622 | p.Cys20Arg | missense_variant | 0.15 |
Rv3236c | 3612388 | c.729T>C | synonymous_variant | 0.5 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641545 | p.Pro4Leu | missense_variant | 0.18 |
alr | 3840248 | c.1173C>A | synonymous_variant | 0.15 |
alr | 3840555 | p.Ala289Val | missense_variant | 0.15 |
alr | 3840913 | p.Ala170Thr | missense_variant | 0.13 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.28 |
rpoA | 3877471 | p.Gln346Arg | missense_variant | 0.17 |
rpoA | 3877591 | p.Leu306Pro | missense_variant | 0.14 |
rpoA | 3877839 | c.669G>T | synonymous_variant | 0.14 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.14 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.18 |
rpoA | 3877881 | c.627G>T | synonymous_variant | 0.18 |
rpoA | 3877884 | c.624G>C | synonymous_variant | 0.18 |
rpoA | 3877893 | c.615C>T | synonymous_variant | 0.22 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.22 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.22 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.22 |
rpoA | 3877926 | c.582G>C | synonymous_variant | 0.29 |
rpoA | 3877929 | c.579C>T | synonymous_variant | 0.29 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.2 |
ddn | 3986654 | c.-190C>A | upstream_gene_variant | 0.18 |
ddn | 3987026 | c.183C>A | synonymous_variant | 0.17 |
clpC1 | 4038286 | p.Trp807Arg | missense_variant | 0.33 |
clpC1 | 4038605 | p.Glu700Asp | missense_variant | 0.22 |
clpC1 | 4038882 | p.Gly608Asp | missense_variant | 0.2 |
clpC1 | 4039090 | c.1615C>T | synonymous_variant | 0.29 |
clpC1 | 4039259 | p.Glu482Asp | missense_variant | 0.33 |
clpC1 | 4039447 | p.Asp420Asn | missense_variant | 0.29 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.18 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.4 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.13 |
clpC1 | 4039874 | p.Asn277Lys | missense_variant | 0.12 |
clpC1 | 4039888 | p.Leu273Ile | missense_variant | 0.13 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.15 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.18 |
clpC1 | 4039949 | c.756G>T | synonymous_variant | 0.29 |
clpC1 | 4039975 | p.Asp244Asn | missense_variant | 0.22 |
embC | 4241072 | p.Leu404Met | missense_variant | 0.22 |
embC | 4241439 | p.Ser526Asn | missense_variant | 0.22 |
embC | 4241712 | p.Arg617Leu | missense_variant | 0.25 |
embC | 4241733 | p.Ala624Val | missense_variant | 0.18 |
embC | 4241864 | c.2002C>T | synonymous_variant | 0.25 |
embA | 4242307 | c.-926C>A | upstream_gene_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242826 | c.-407G>T | upstream_gene_variant | 0.29 |
embC | 4242900 | p.Pro1013Arg | missense_variant | 0.14 |
embC | 4242967 | p.Ile1035Met | missense_variant | 0.13 |
embA | 4243318 | p.Gly29Asp | missense_variant | 0.29 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244850 | p.Arg540Trp | missense_variant | 0.25 |
embA | 4244891 | c.1659C>T | synonymous_variant | 0.25 |
embA | 4245757 | p.Ser842Ile | missense_variant | 0.22 |
embA | 4246176 | p.Ala982Thr | missense_variant | 0.29 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.62 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.5 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4246718 | p.Ala69Pro | missense_variant | 0.25 |
embB | 4249676 | p.Arg1055Gly | missense_variant | 0.25 |
embB | 4249757 | p.Thr1082Ala | missense_variant | 1.0 |
aftB | 4267002 | p.Arg612Pro | missense_variant | 0.22 |
aftB | 4267025 | c.1812C>T | synonymous_variant | 0.14 |
aftB | 4267031 | c.1806C>A | synonymous_variant | 0.14 |
aftB | 4267370 | c.1467C>T | synonymous_variant | 0.25 |
aftB | 4267490 | c.1347G>A | synonymous_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269116 | p.Arg240Cys | missense_variant | 1.0 |
ubiA | 4269437 | p.Ala133Ser | missense_variant | 0.14 |
ethA | 4326405 | p.Asp357Tyr | missense_variant | 1.0 |
ethA | 4327353 | p.Met41Val | missense_variant | 0.14 |
ethA | 4327430 | p.Ser15Tyr | missense_variant | 0.18 |
ethA | 4327701 | c.-228G>T | upstream_gene_variant | 0.18 |
ethR | 4327933 | p.Ala129Thr | missense_variant | 0.25 |
whiB6 | 4338381 | p.Asp47Glu | missense_variant | 0.5 |
whiB6 | 4338399 | p.Trp41Cys | missense_variant | 0.5 |
whiB6 | 4338436 | p.Val29Pro | missense_variant | 0.33 |
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 | 4408085 | p.Glu40* | stop_gained | 0.17 |