Run ID: ERR5864140
Sample name:
Date: 01-04-2023 23:08:49
Number of reads: 288306
Percentage reads mapped: 99.35
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2154463 | p.Ala550Asp | missense_variant | 0.22 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289072 | p.His57Arg | missense_variant | 1.0 | pyrazinamide |
embA | 4243222 | c.-11C>A | upstream_gene_variant | 0.4 | ethambutol |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6005 | p.Gly256Cys | missense_variant | 0.27 |
gyrB | 6117 | p.Trp293Leu | missense_variant | 0.22 |
gyrB | 6139 | c.900G>T | synonymous_variant | 0.33 |
gyrB | 6175 | p.Glu312Asp | missense_variant | 0.25 |
gyrB | 7156 | p.Asp639Glu | missense_variant | 0.2 |
gyrA | 7296 | c.-6G>T | upstream_gene_variant | 0.22 |
gyrA | 7321 | p.Pro7Gln | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7521 | p.Ala74Thr | missense_variant | 0.22 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7973 | c.672A>G | synonymous_variant | 0.13 |
gyrA | 8333 | p.Asn344Lys | missense_variant | 0.18 |
gyrA | 8689 | p.Ala463Asp | missense_variant | 0.29 |
gyrA | 8694 | p.Leu465Met | missense_variant | 0.29 |
gyrA | 9183 | p.Arg628Ser | missense_variant | 0.22 |
gyrA | 9192 | p.Leu631Met | missense_variant | 0.22 |
gyrA | 9286 | p.Ala662Glu | missense_variant | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9356 | c.2055G>T | synonymous_variant | 0.25 |
gyrA | 9513 | p.Glu738* | stop_gained | 0.4 |
fgd1 | 490738 | c.-45C>T | upstream_gene_variant | 0.29 |
fgd1 | 491037 | c.255C>A | synonymous_variant | 0.2 |
fgd1 | 491422 | p.Gly214Cys | missense_variant | 0.4 |
fgd1 | 491719 | p.Pro313Thr | missense_variant | 0.29 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575379 | p.Gly11Val | missense_variant | 0.29 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575917 | c.570C>T | synonymous_variant | 0.5 |
mshA | 576101 | c.754C>A | synonymous_variant | 0.25 |
mshA | 576148 | c.801G>T | synonymous_variant | 0.33 |
mshA | 576228 | p.Arg294Leu | missense_variant | 0.25 |
mshA | 576450 | p.Pro368Gln | missense_variant | 0.4 |
ccsA | 619750 | c.-141C>A | upstream_gene_variant | 0.18 |
ccsA | 620000 | p.Ala37Asp | missense_variant | 0.33 |
ccsA | 620233 | p.Asn115Tyr | missense_variant | 0.4 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620678 | p.Pro263His | missense_variant | 0.5 |
ccsA | 620767 | p.Ala293Thr | missense_variant | 0.33 |
ccsA | 620824 | p.Leu312Met | missense_variant | 0.4 |
rpoB | 759889 | p.Gly28Val | missense_variant | 0.22 |
rpoB | 760011 | p.Ala69Thr | missense_variant | 0.25 |
rpoB | 760124 | p.Phe106Leu | missense_variant | 0.22 |
rpoB | 760165 | p.Asp120Val | missense_variant | 0.17 |
rpoB | 760330 | p.Arg175Leu | missense_variant | 0.22 |
rpoB | 760768 | p.Pro321His | missense_variant | 0.22 |
rpoB | 760935 | p.Glu377* | stop_gained | 0.29 |
rpoB | 761031 | p.Gln409Lys | missense_variant | 0.25 |
rpoB | 761184 | p.Glu460Lys | missense_variant | 0.29 |
rpoB | 761372 | c.1566C>A | synonymous_variant | 0.67 |
rpoB | 761419 | p.Ala538Asp | missense_variant | 0.67 |
rpoB | 761516 | c.1710G>T | synonymous_variant | 0.5 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.29 |
rpoB | 761872 | p.Arg689Gln | missense_variant | 0.33 |
rpoB | 762168 | p.Ala788Ser | missense_variant | 0.2 |
rpoB | 762539 | p.Leu911Phe | missense_variant | 0.25 |
rpoB | 762549 | p.Gly915Cys | missense_variant | 0.29 |
rpoB | 762691 | p.Pro962Gln | missense_variant | 0.25 |
rpoC | 762698 | c.-672C>A | upstream_gene_variant | 0.25 |
rpoB | 762881 | p.Met1025Ile | missense_variant | 0.25 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764030 | p.Asp221Tyr | missense_variant | 0.23 |
rpoC | 764233 | p.Lys288Asn | missense_variant | 0.18 |
rpoC | 764654 | p.Val429Phe | missense_variant | 0.2 |
rpoC | 764802 | p.Arg478Leu | missense_variant | 0.29 |
rpoC | 765345 | p.Gly659Val | missense_variant | 0.25 |
rpoC | 765521 | p.Asp718Tyr | missense_variant | 0.22 |
rpoC | 766177 | c.2808C>A | synonymous_variant | 0.2 |
rpoC | 766249 | c.2880C>A | synonymous_variant | 0.25 |
rpoC | 766737 | p.Arg1123Gln | missense_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775862 | c.2619G>T | synonymous_variant | 0.2 |
mmpL5 | 776066 | c.2415C>A | synonymous_variant | 0.4 |
mmpL5 | 776089 | p.Val798Ile | missense_variant | 0.5 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776136 | p.Ser782Tyr | missense_variant | 0.25 |
mmpL5 | 776145 | p.Ala779Asp | missense_variant | 0.29 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776445 | p.Ala679Val | missense_variant | 0.18 |
mmpL5 | 776520 | p.Ser654Ile | missense_variant | 0.17 |
mmpL5 | 777024 | p.Arg486Leu | missense_variant | 0.18 |
mmpL5 | 777032 | c.1449C>A | synonymous_variant | 0.18 |
mmpL5 | 777118 | p.Asp455Tyr | missense_variant | 0.25 |
mmpL5 | 777434 | c.1047C>A | synonymous_variant | 0.25 |
mmpL5 | 777705 | p.Ser259* | stop_gained | 0.4 |
mmpL5 | 777752 | c.729C>A | synonymous_variant | 0.33 |
mmpL5 | 777761 | c.720G>A | synonymous_variant | 0.33 |
mmpL5 | 777795 | p.Ser229* | stop_gained | 0.3 |
mmpL5 | 777807 | p.Ser225* | stop_gained | 0.22 |
mmpL5 | 777821 | c.660G>A | synonymous_variant | 0.2 |
mmpL5 | 777880 | p.Asp201Tyr | missense_variant | 0.22 |
mmpL5 | 777891 | p.Gln197Leu | missense_variant | 0.2 |
mmpR5 | 778373 | c.-617G>T | upstream_gene_variant | 0.29 |
mmpS5 | 778554 | p.Val118Ile | missense_variant | 0.29 |
mmpL5 | 778558 | c.-78C>A | upstream_gene_variant | 0.29 |
mmpR5 | 779006 | p.Gly6Val | missense_variant | 0.2 |
mmpS5 | 779515 | c.-610C>A | upstream_gene_variant | 0.29 |
mmpS5 | 779568 | c.-663C>A | upstream_gene_variant | 0.17 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
mmpS5 | 779625 | c.-720G>T | upstream_gene_variant | 0.2 |
mmpS5 | 779676 | c.-771C>A | upstream_gene_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781599 | p.Asp14Tyr | missense_variant | 0.33 |
rplC | 800651 | c.-158G>T | upstream_gene_variant | 0.2 |
rplC | 800775 | c.-34G>T | upstream_gene_variant | 0.25 |
rplC | 801223 | p.His139Asn | missense_variant | 0.29 |
rplC | 801387 | c.579G>T | synonymous_variant | 0.38 |
rplC | 801426 | c.618C>A | synonymous_variant | 0.2 |
fbiC | 1302956 | p.Ser9Tyr | missense_variant | 0.5 |
fbiC | 1303114 | p.Ala62Ser | missense_variant | 0.2 |
fbiC | 1303154 | p.Arg75Leu | missense_variant | 0.18 |
fbiC | 1303170 | c.240C>A | synonymous_variant | 0.22 |
fbiC | 1303627 | p.Ser233Gly | missense_variant | 0.18 |
fbiC | 1303942 | p.Val338Leu | missense_variant | 0.29 |
fbiC | 1304013 | c.1083G>T | synonymous_variant | 0.4 |
fbiC | 1304225 | p.Gly432Asp | missense_variant | 0.17 |
fbiC | 1304275 | p.Leu449Met | missense_variant | 0.22 |
fbiC | 1304382 | c.1452G>T | synonymous_variant | 0.2 |
fbiC | 1304675 | p.Gly582Val | missense_variant | 0.29 |
fbiC | 1304807 | p.Pro626His | missense_variant | 0.4 |
fbiC | 1305222 | c.2292C>A | synonymous_variant | 0.29 |
fbiC | 1305285 | p.Gln785His | missense_variant | 0.22 |
Rv1258c | 1406094 | p.Gly416Val | missense_variant | 0.25 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406963 | c.378G>T | synonymous_variant | 0.4 |
Rv1258c | 1407329 | p.Ser4Arg | missense_variant | 0.2 |
Rv1258c | 1407354 | c.-14C>A | upstream_gene_variant | 0.22 |
Rv1258c | 1407410 | c.-70C>A | upstream_gene_variant | 0.33 |
embR | 1416240 | p.Arg370Ser | missense_variant | 0.25 |
embR | 1416314 | p.Arg345Leu | missense_variant | 0.29 |
embR | 1416321 | p.Asp343Tyr | missense_variant | 0.29 |
embR | 1416554 | p.Ser265Tyr | missense_variant | 0.25 |
embR | 1416708 | p.Ala214Ser | missense_variant | 0.29 |
embR | 1416815 | p.Ala178Glu | missense_variant | 0.33 |
embR | 1416934 | c.414G>A | synonymous_variant | 0.33 |
embR | 1417138 | c.210G>T | synonymous_variant | 0.4 |
embR | 1417212 | p.Arg46Ser | missense_variant | 0.2 |
embR | 1417216 | c.132C>A | synonymous_variant | 0.22 |
embR | 1417228 | c.120C>A | synonymous_variant | 0.2 |
embR | 1417421 | c.-74G>T | upstream_gene_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472049 | n.204G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472098 | n.253G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472190 | n.345G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472270 | n.425T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472568 | n.723C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473435 | n.-223C>A | upstream_gene_variant | 0.25 |
rrl | 1473525 | n.-133C>A | upstream_gene_variant | 0.25 |
rrl | 1474198 | n.541G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474277 | n.620C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474470 | n.813G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474566 | n.909G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474827 | n.1170C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475186 | n.1529C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475396 | n.1739C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475400 | n.1743C>A | non_coding_transcript_exon_variant | 0.6 |
fabG1 | 1673411 | c.-29C>T | upstream_gene_variant | 0.4 |
fabG1 | 1673489 | p.Ser17* | stop_gained | 0.33 |
fabG1 | 1673501 | p.Thr21Asn | missense_variant | 0.33 |
fabG1 | 1673858 | p.Ser140* | stop_gained | 0.29 |
fabG1 | 1673971 | p.Ala178Ser | missense_variant | 0.17 |
inhA | 1674222 | c.21C>A | synonymous_variant | 0.33 |
inhA | 1674276 | c.75C>A | synonymous_variant | 0.22 |
inhA | 1674364 | p.Pro55Ser | missense_variant | 0.33 |
inhA | 1674373 | p.Ala58Ser | missense_variant | 0.22 |
inhA | 1674414 | c.213G>T | synonymous_variant | 0.22 |
inhA | 1674454 | p.Gly85Cys | missense_variant | 0.2 |
inhA | 1674551 | p.Ser117Tyr | missense_variant | 0.3 |
inhA | 1674763 | p.Leu188Ile | missense_variant | 0.23 |
inhA | 1674775 | p.Gly192Cys | missense_variant | 0.15 |
rpsA | 1833424 | c.-118C>A | upstream_gene_variant | 0.22 |
rpsA | 1833658 | c.117C>A | synonymous_variant | 0.25 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834397 | p.His286Asn | missense_variant | 0.33 |
rpsA | 1834499 | p.Leu320Met | missense_variant | 0.4 |
rpsA | 1834741 | c.1200C>A | synonymous_variant | 0.33 |
tlyA | 1917771 | c.-169G>T | upstream_gene_variant | 0.29 |
tlyA | 1917813 | c.-127C>A | upstream_gene_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918080 | c.141C>A | synonymous_variant | 0.29 |
tlyA | 1918180 | p.Val81Met | missense_variant | 0.4 |
tlyA | 1918287 | c.348C>A | synonymous_variant | 0.2 |
ndh | 2101655 | p.Ser463Ile | missense_variant | 0.25 |
ndh | 2101880 | p.Ser388Ile | missense_variant | 0.17 |
ndh | 2102065 | c.978G>A | synonymous_variant | 0.25 |
ndh | 2102981 | p.Gly21Val | missense_variant | 0.25 |
katG | 2154037 | p.Ser692Ile | missense_variant | 0.18 |
katG | 2154417 | c.1695G>T | synonymous_variant | 0.22 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154804 | c.1308G>A | synonymous_variant | 0.2 |
katG | 2154842 | p.Ala424Ser | missense_variant | 0.2 |
katG | 2155310 | p.Gly268Cys | missense_variant | 0.29 |
katG | 2155495 | p.Gly206Val | missense_variant | 0.22 |
katG | 2155656 | p.Lys152Asn | missense_variant | 0.2 |
katG | 2155659 | c.453C>A | synonymous_variant | 0.18 |
katG | 2155863 | c.249G>T | synonymous_variant | 0.25 |
katG | 2155871 | p.Glu81* | stop_gained | 0.25 |
katG | 2155877 | p.Asp79Tyr | missense_variant | 0.25 |
katG | 2156220 | c.-109G>T | upstream_gene_variant | 0.25 |
katG | 2156235 | c.-124G>T | upstream_gene_variant | 0.25 |
PPE35 | 2167712 | c.2901C>A | synonymous_variant | 0.3 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167954 | p.Tyr887His | missense_variant | 0.13 |
PPE35 | 2168045 | p.Leu856Phe | missense_variant | 0.29 |
PPE35 | 2168084 | p.Glu843Asp | missense_variant | 0.22 |
PPE35 | 2168354 | c.2259G>T | synonymous_variant | 0.67 |
PPE35 | 2169751 | p.Gly288* | stop_gained | 0.43 |
PPE35 | 2169964 | p.Leu217Ile | missense_variant | 0.29 |
PPE35 | 2170018 | p.Ala199Ser | missense_variant | 0.33 |
PPE35 | 2170025 | c.588G>T | synonymous_variant | 0.33 |
PPE35 | 2170032 | p.Gly194Val | missense_variant | 0.33 |
PPE35 | 2170210 | p.Ala135Thr | missense_variant | 0.2 |
Rv1979c | 2221755 | c.1410C>A | synonymous_variant | 0.23 |
Rv1979c | 2222022 | c.1143C>A | synonymous_variant | 0.2 |
Rv1979c | 2222209 | p.Ala319Asp | missense_variant | 0.27 |
Rv1979c | 2222334 | c.831C>A | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288728 | p.Leu172Met | missense_variant | 0.18 |
pncA | 2289221 | c.21C>A | synonymous_variant | 0.25 |
pncA | 2289527 | c.-286C>A | upstream_gene_variant | 0.25 |
pncA | 2289563 | c.-322G>T | upstream_gene_variant | 0.22 |
pncA | 2290222 | c.-981C>A | upstream_gene_variant | 0.22 |
kasA | 2517977 | c.-138C>T | upstream_gene_variant | 0.22 |
kasA | 2518167 | p.Ala18Asp | missense_variant | 0.18 |
kasA | 2518413 | p.Ser100Ile | missense_variant | 0.4 |
kasA | 2518424 | p.Asp104Tyr | missense_variant | 0.4 |
kasA | 2518467 | p.Gly118Val | missense_variant | 0.4 |
kasA | 2519158 | c.1044C>T | synonymous_variant | 0.25 |
eis | 2714179 | p.Arg385Leu | missense_variant | 0.22 |
eis | 2714308 | p.Pro342Gln | missense_variant | 0.43 |
eis | 2714411 | p.Arg308Ser | missense_variant | 0.29 |
eis | 2714459 | p.Asp292Tyr | missense_variant | 0.29 |
eis | 2714546 | p.Glu263* | stop_gained | 0.3 |
eis | 2714668 | p.Gly222Val | missense_variant | 0.18 |
eis | 2715400 | c.-68C>A | upstream_gene_variant | 0.25 |
eis | 2715495 | c.-163G>T | upstream_gene_variant | 0.22 |
eis | 2715585 | c.-253C>A | upstream_gene_variant | 0.29 |
ahpC | 2726084 | c.-109C>A | upstream_gene_variant | 0.22 |
ahpC | 2726316 | p.Glu42* | stop_gained | 0.2 |
ahpC | 2726586 | p.Asp132Tyr | missense_variant | 0.22 |
folC | 2747731 | c.-133C>A | upstream_gene_variant | 0.25 |
folC | 2747779 | c.-181G>A | upstream_gene_variant | 0.25 |
pepQ | 2859324 | p.Phe365Leu | missense_variant | 0.29 |
pepQ | 2859477 | c.942T>C | synonymous_variant | 0.29 |
pepQ | 2859928 | p.Arg164Leu | missense_variant | 0.29 |
pepQ | 2860160 | p.Ala87Ser | missense_variant | 0.33 |
pepQ | 2860181 | p.Gly80Trp | missense_variant | 0.25 |
pepQ | 2860484 | c.-66G>A | upstream_gene_variant | 0.67 |
ribD | 2986654 | c.-185C>A | upstream_gene_variant | 0.2 |
ribD | 2986668 | c.-171C>A | upstream_gene_variant | 0.2 |
ribD | 2987292 | p.Thr152Ala | missense_variant | 0.15 |
ribD | 2987375 | c.537G>T | synonymous_variant | 0.2 |
Rv2752c | 3064584 | c.1608G>T | synonymous_variant | 0.29 |
Rv2752c | 3064755 | c.1437C>A | synonymous_variant | 0.33 |
Rv2752c | 3064773 | c.1419C>A | synonymous_variant | 0.33 |
Rv2752c | 3064786 | p.Ser469* | stop_gained | 0.29 |
Rv2752c | 3064911 | c.1281C>A | synonymous_variant | 0.36 |
Rv2752c | 3065290 | p.Val301Ala | missense_variant | 0.12 |
Rv2752c | 3065413 | p.Ser260* | stop_gained | 0.22 |
Rv2752c | 3065420 | c.772C>A | synonymous_variant | 0.22 |
Rv2752c | 3066282 | c.-91G>T | upstream_gene_variant | 0.22 |
Rv2752c | 3067083 | c.-892C>A | upstream_gene_variant | 0.25 |
Rv2752c | 3067166 | c.-975G>A | upstream_gene_variant | 0.2 |
Rv2752c | 3067182 | c.-991C>A | upstream_gene_variant | 0.27 |
thyX | 3067310 | c.636C>A | synonymous_variant | 0.2 |
thyX | 3067408 | p.Glu180* | stop_gained | 0.25 |
thyX | 3067468 | p.Ala160Ser | missense_variant | 1.0 |
thyX | 3067955 | c.-10G>T | upstream_gene_variant | 0.25 |
thyX | 3067990 | c.-45C>T | upstream_gene_variant | 0.2 |
thyX | 3068046 | c.-101G>T | upstream_gene_variant | 0.22 |
thyA | 3073860 | c.612C>A | synonymous_variant | 0.2 |
thyA | 3074260 | p.Trp71Leu | missense_variant | 0.2 |
thyA | 3074337 | c.135C>A | synonymous_variant | 0.2 |
thyA | 3074438 | p.Leu12Phe | missense_variant | 0.25 |
thyA | 3074523 | c.-52G>T | upstream_gene_variant | 0.25 |
thyA | 3074536 | c.-65G>T | upstream_gene_variant | 0.25 |
ald | 3086650 | c.-170C>A | upstream_gene_variant | 0.33 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086879 | c.60G>T | synonymous_variant | 0.29 |
ald | 3087123 | p.Ala102Thr | missense_variant | 0.4 |
ald | 3087286 | p.Arg156Leu | missense_variant | 0.25 |
ald | 3087322 | p.Pro168Gln | missense_variant | 0.29 |
ald | 3087544 | p.Pro242Gln | missense_variant | 0.2 |
ald | 3087874 | p.Ser352Tyr | missense_variant | 0.33 |
fbiD | 3339423 | c.306G>T | synonymous_variant | 0.33 |
fbiD | 3339735 | c.618G>T | synonymous_variant | 0.29 |
Rv3083 | 3448794 | p.Lys97Asn | missense_variant | 0.29 |
Rv3083 | 3448809 | c.306G>T | synonymous_variant | 0.29 |
Rv3083 | 3449032 | p.Gly177Cys | missense_variant | 0.33 |
Rv3083 | 3449207 | p.Pro235Gln | missense_variant | 0.33 |
Rv3083 | 3449454 | c.951G>T | synonymous_variant | 0.67 |
Rv3083 | 3449518 | p.Ala339Ser | missense_variant | 0.67 |
Rv3083 | 3449554 | p.Gln351Lys | missense_variant | 1.0 |
Rv3083 | 3449776 | p.Asp425Asn | missense_variant | 0.29 |
fprA | 3473833 | c.-174G>T | upstream_gene_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474255 | c.249C>A | synonymous_variant | 0.33 |
fprA | 3474279 | c.273C>A | synonymous_variant | 0.22 |
fprA | 3474660 | c.654C>A | synonymous_variant | 0.5 |
fprA | 3475059 | p.Ser351Arg | missense_variant | 0.4 |
fprA | 3475064 | p.Asn353Ser | missense_variant | 0.33 |
fprA | 3475104 | c.1098G>T | synonymous_variant | 0.4 |
fprA | 3475294 | p.Glu430* | stop_gained | 0.22 |
whiB7 | 3568574 | p.Leu36Ile | missense_variant | 0.18 |
whiB7 | 3568716 | c.-37G>T | upstream_gene_variant | 0.27 |
Rv3236c | 3612450 | p.Leu223Met | missense_variant | 0.2 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3612946 | p.Phe57Leu | missense_variant | 0.22 |
Rv3236c | 3613043 | p.Ala25Glu | missense_variant | 0.22 |
fbiA | 3640522 | c.-21C>A | upstream_gene_variant | 0.33 |
fbiB | 3640554 | c.-981C>A | upstream_gene_variant | 0.18 |
fbiB | 3640665 | c.-870G>T | upstream_gene_variant | 0.3 |
fbiA | 3640932 | p.Glu130Asp | missense_variant | 0.33 |
fbiB | 3641325 | c.-210G>A | upstream_gene_variant | 0.5 |
fbiB | 3641475 | c.-60C>T | upstream_gene_variant | 0.5 |
fbiB | 3641737 | p.Glu68Val | missense_variant | 0.67 |
fbiB | 3642223 | p.Arg230Leu | missense_variant | 0.21 |
fbiB | 3642484 | p.Trp317Leu | missense_variant | 0.22 |
fbiB | 3642490 | p.Ser319Tyr | missense_variant | 0.25 |
alr | 3840420 | p.Arg334Leu | missense_variant | 0.25 |
alr | 3840423 | p.Arg333Ile | missense_variant | 0.25 |
alr | 3840451 | p.Gly324Trp | missense_variant | 0.4 |
alr | 3840530 | c.891C>T | synonymous_variant | 0.2 |
alr | 3840535 | p.Gly296Trp | missense_variant | 0.2 |
alr | 3840619 | p.Asp268Tyr | missense_variant | 0.18 |
alr | 3840673 | p.Leu250Met | missense_variant | 0.2 |
alr | 3840790 | p.Gln211Lys | missense_variant | 0.22 |
alr | 3841187 | c.234C>A | synonymous_variant | 0.25 |
alr | 3841194 | p.Arg76Leu | missense_variant | 0.25 |
alr | 3841297 | p.Leu42Met | missense_variant | 0.2 |
alr | 3841313 | c.108C>A | synonymous_variant | 0.22 |
alr | 3841366 | p.Gly19Cys | missense_variant | 0.25 |
alr | 3841371 | p.Gly17Val | missense_variant | 0.25 |
rpoA | 3877620 | p.Glu296Asp | missense_variant | 0.22 |
rpoA | 3877665 | c.843C>A | synonymous_variant | 0.27 |
rpoA | 3877801 | p.Pro236Gln | missense_variant | 0.22 |
rpoA | 3877821 | c.687C>A | synonymous_variant | 0.2 |
rpoA | 3878088 | c.420C>A | synonymous_variant | 0.29 |
rpoA | 3878172 | c.336G>T | synonymous_variant | 0.25 |
rpoA | 3878416 | p.Gly31Asp | missense_variant | 0.25 |
rpoA | 3878463 | c.45C>A | synonymous_variant | 0.2 |
ddn | 3986758 | c.-86G>T | upstream_gene_variant | 0.22 |
ddn | 3987200 | c.357C>T | synonymous_variant | 0.33 |
clpC1 | 4038226 | p.Pro827Ser | missense_variant | 0.5 |
clpC1 | 4038317 | c.2388G>T | synonymous_variant | 0.4 |
clpC1 | 4038933 | p.Ala591Glu | missense_variant | 0.4 |
clpC1 | 4039028 | p.Lys559Asn | missense_variant | 0.4 |
clpC1 | 4039294 | p.Gly471Cys | missense_variant | 0.18 |
clpC1 | 4039541 | c.1164C>A | synonymous_variant | 0.22 |
clpC1 | 4039682 | c.1023C>A | synonymous_variant | 0.29 |
clpC1 | 4039761 | p.Gly315Val | missense_variant | 0.33 |
clpC1 | 4039763 | c.942C>T | synonymous_variant | 0.33 |
clpC1 | 4039996 | p.Glu237* | stop_gained | 0.22 |
clpC1 | 4040880 | c.-176G>T | upstream_gene_variant | 0.29 |
panD | 4044048 | p.Leu78Phe | missense_variant | 0.4 |
panD | 4044069 | c.213C>A | synonymous_variant | 0.4 |
panD | 4044224 | p.Leu20Met | missense_variant | 0.5 |
panD | 4044326 | c.-45C>A | upstream_gene_variant | 0.22 |
panD | 4044434 | c.-153G>T | upstream_gene_variant | 0.22 |
embC | 4239671 | c.-192C>A | upstream_gene_variant | 0.22 |
embC | 4239758 | c.-105C>A | upstream_gene_variant | 0.5 |
embC | 4240093 | c.231C>T | synonymous_variant | 0.2 |
embC | 4240139 | p.Gly93* | stop_gained | 0.18 |
embC | 4240847 | p.Asp329Tyr | missense_variant | 0.29 |
embC | 4241106 | p.Arg415Leu | missense_variant | 0.33 |
embC | 4241392 | c.1530G>T | synonymous_variant | 0.2 |
embC | 4241514 | p.Ser551* | stop_gained | 0.33 |
embC | 4241575 | c.1713C>A | synonymous_variant | 0.4 |
embC | 4241764 | p.Phe634Leu | missense_variant | 0.29 |
embC | 4241773 | c.1911C>A | synonymous_variant | 0.29 |
embC | 4241853 | p.Ala664Glu | missense_variant | 0.22 |
embC | 4241937 | p.Arg692Met | missense_variant | 0.15 |
embC | 4241980 | c.2118C>A | synonymous_variant | 0.44 |
embC | 4242354 | p.Gly831Val | missense_variant | 0.5 |
embC | 4242572 | p.Glu904* | stop_gained | 0.22 |
embC | 4242588 | p.Gly909Val | missense_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243565 | p.Gln111His | missense_variant | 0.33 |
embA | 4243580 | c.348G>T | synonymous_variant | 0.33 |
embA | 4243770 | p.Gly180* | stop_gained | 0.22 |
embA | 4243800 | p.Asp190Tyr | missense_variant | 0.22 |
embA | 4243844 | c.612G>A | synonymous_variant | 0.2 |
embA | 4243862 | c.630C>A | synonymous_variant | 0.25 |
embA | 4243866 | p.Leu212Met | missense_variant | 0.22 |
embA | 4245056 | c.1824C>A | synonymous_variant | 0.33 |
embA | 4245585 | p.Pro785Thr | missense_variant | 0.2 |
embA | 4245708 | p.Ala826Ser | missense_variant | 0.18 |
embA | 4245799 | p.Trp856Leu | missense_variant | 0.22 |
embA | 4245847 | p.Ser872Tyr | missense_variant | 0.29 |
embB | 4245851 | c.-663G>A | upstream_gene_variant | 0.29 |
embA | 4245868 | p.Ser879Tyr | missense_variant | 0.5 |
embB | 4245899 | c.-615C>A | upstream_gene_variant | 0.33 |
embB | 4245908 | c.-606G>T | upstream_gene_variant | 0.5 |
embA | 4245958 | p.Gly909Val | missense_variant | 0.4 |
embB | 4246307 | c.-207G>T | upstream_gene_variant | 0.5 |
embA | 4246311 | p.Gly1027Cys | missense_variant | 0.33 |
embA | 4246428 | p.Ala1066Thr | missense_variant | 0.29 |
embB | 4246682 | p.Asp57Tyr | missense_variant | 0.25 |
embB | 4246762 | c.249G>T | synonymous_variant | 0.29 |
embB | 4246954 | c.441C>T | synonymous_variant | 0.29 |
embB | 4246960 | p.Glu149Asp | missense_variant | 0.29 |
embB | 4247009 | p.Asp166Tyr | missense_variant | 0.29 |
embB | 4247027 | p.Leu172Met | missense_variant | 0.25 |
embB | 4247398 | c.885G>T | synonymous_variant | 0.25 |
embB | 4247408 | p.Asp299Tyr | missense_variant | 0.25 |
embB | 4247428 | c.915C>A | synonymous_variant | 0.29 |
embB | 4247726 | p.Glu405* | stop_gained | 0.29 |
embB | 4248076 | p.Glu521Asp | missense_variant | 0.29 |
embB | 4248460 | c.1947C>A | synonymous_variant | 0.25 |
embB | 4248493 | p.Met660Ile | missense_variant | 0.22 |
embB | 4248571 | c.2058G>T | synonymous_variant | 0.22 |
embB | 4248976 | c.2463G>T | synonymous_variant | 0.21 |
embB | 4249340 | p.Ala943Thr | missense_variant | 0.22 |
embB | 4249378 | c.2865G>T | synonymous_variant | 0.2 |
embB | 4249489 | p.Leu992Phe | missense_variant | 0.29 |
embB | 4249510 | c.2997G>T | synonymous_variant | 0.29 |
embB | 4249647 | p.Arg1045Leu | missense_variant | 0.4 |
embB | 4249679 | p.Asp1056Tyr | missense_variant | 0.25 |
embB | 4249770 | p.Ser1086Ile | missense_variant | 0.25 |
aftB | 4267080 | p.Arg586Leu | missense_variant | 0.5 |
aftB | 4267123 | c.1714C>A | synonymous_variant | 0.5 |
aftB | 4267274 | c.1563G>T | synonymous_variant | 0.22 |
aftB | 4267403 | p.Pro478Gln | missense_variant | 0.18 |
aftB | 4267583 | c.1254C>A | synonymous_variant | 0.33 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267670 | c.1167G>T | synonymous_variant | 0.5 |
aftB | 4268097 | p.Gly247Asp | missense_variant | 0.2 |
aftB | 4268231 | c.606C>T | synonymous_variant | 0.4 |
aftB | 4268251 | p.Ala196Ser | missense_variant | 0.67 |
aftB | 4268543 | c.294C>A | synonymous_variant | 0.67 |
aftB | 4268831 | c.6C>T | synonymous_variant | 0.29 |
ubiA | 4269029 | p.Gly269Cys | missense_variant | 0.25 |
ubiA | 4269367 | p.Ala156Glu | missense_variant | 0.25 |
ubiA | 4269397 | p.Ala146Glu | missense_variant | 0.33 |
ubiA | 4269672 | p.Lys54Asn | missense_variant | 0.2 |
ubiA | 4269710 | p.Gly42Cys | missense_variant | 0.18 |
aftB | 4269711 | c.-875C>T | upstream_gene_variant | 0.17 |
aftB | 4269780 | c.-944C>A | upstream_gene_variant | 0.25 |
aftB | 4269792 | c.-956C>A | upstream_gene_variant | 0.29 |
ethA | 4326181 | p.Phe431Leu | missense_variant | 0.21 |
ethA | 4326350 | p.Ser375Phe | missense_variant | 0.17 |
ethA | 4326714 | p.Gln254Lys | missense_variant | 0.2 |
ethR | 4326868 | c.-681G>T | upstream_gene_variant | 0.38 |
ethR | 4327159 | c.-390G>A | upstream_gene_variant | 0.29 |
ethA | 4327191 | p.Asp95Tyr | missense_variant | 0.2 |
ethR | 4327390 | c.-159C>A | upstream_gene_variant | 0.33 |
ethR | 4327601 | p.Ala18Val | missense_variant | 0.18 |
ethR | 4327862 | p.Thr105Ile | missense_variant | 0.2 |
ethA | 4328064 | c.-591G>T | upstream_gene_variant | 0.22 |
whiB6 | 4338371 | p.Thr51Pro | missense_variant | 1.0 |
whiB6 | 4338464 | p.Asp20Tyr | missense_variant | 0.18 |
whiB6 | 4338489 | c.33C>A | synonymous_variant | 0.17 |
whiB6 | 4338585 | c.-64G>T | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407531 | c.672G>T | synonymous_variant | 0.22 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407813 | c.390C>A | synonymous_variant | 0.17 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408091 | p.Pro38Thr | missense_variant | 0.14 |