Run ID: ERR6336752
Sample name:
Date: 02-04-2023 02:02:09
Number of reads: 1282011
Percentage reads mapped: 98.78
Strain: lineage1.2.1.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 1.0 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155786 | p.Ala109Val | missense_variant | 0.2 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7445 | c.144C>T | synonymous_variant | 0.25 |
gyrA | 7446 | p.Lys49Glu | missense_variant | 0.25 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7635 | p.Gly112Ser | missense_variant | 0.2 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9071 | c.1770_1771insC | frameshift_variant | 0.12 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9189 | p.Gly630Arg | missense_variant | 0.11 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9293 | c.1992G>A | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490715 | c.-68A>G | upstream_gene_variant | 0.14 |
fgd1 | 490872 | c.90C>T | synonymous_variant | 0.14 |
fgd1 | 491152 | p.Glu124Lys | missense_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575194 | c.-153delC | upstream_gene_variant | 0.13 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 575398 | c.51T>C | synonymous_variant | 0.4 |
mshA | 575418 | p.Ala24Gly | missense_variant | 0.29 |
mshA | 575752 | c.405G>A | synonymous_variant | 0.12 |
mshA | 576160 | c.813C>T | synonymous_variant | 0.29 |
mshA | 576502 | c.1155C>T | synonymous_variant | 0.5 |
mshA | 576774 | p.Arg476His | missense_variant | 0.12 |
ccsA | 620123 | p.Arg78Leu | missense_variant | 0.33 |
ccsA | 620743 | p.Ala285Pro | missense_variant | 0.14 |
rpoB | 761647 | p.Arg614His | missense_variant | 0.22 |
rpoB | 761701 | p.Ala632Val | missense_variant | 0.29 |
rpoB | 761710 | p.Val635Asp | missense_variant | 0.33 |
rpoB | 761713 | p.Val636Asp | missense_variant | 0.36 |
rpoB | 762131 | c.2325C>T | synonymous_variant | 0.13 |
rpoB | 762208 | p.Thr801Ile | missense_variant | 0.22 |
rpoB | 762223 | p.Thr806Ile | missense_variant | 0.14 |
rpoB | 762945 | p.Thr1047Ala | missense_variant | 0.25 |
rpoB | 762952 | p.Gln1049Arg | missense_variant | 0.19 |
rpoB | 762955 | p.Pro1050Leu | missense_variant | 0.19 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.16 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763610 | p.Glu81Lys | missense_variant | 0.12 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 763965 | p.Asp199Val | missense_variant | 1.0 |
rpoC | 764710 | p.Met447Ile | missense_variant | 1.0 |
rpoC | 765532 | c.2163C>T | synonymous_variant | 0.18 |
rpoC | 766074 | p.Ala902Gly | missense_variant | 0.18 |
rpoC | 766102 | c.2733C>T | synonymous_variant | 0.29 |
rpoC | 766658 | p.Arg1097Trp | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778594 | c.-114C>T | upstream_gene_variant | 0.25 |
mmpR5 | 779279 | p.Pro97Leu | missense_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304082 | c.1152C>T | synonymous_variant | 1.0 |
fbiC | 1304503 | c.1573C>T | synonymous_variant | 0.17 |
fbiC | 1305251 | p.Arg774Leu | missense_variant | 0.15 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406538 | p.Ala268Gly | missense_variant | 0.29 |
Rv1258c | 1406952 | p.Glu130Thr | missense_variant | 0.2 |
Rv1258c | 1407437 | c.-97A>G | upstream_gene_variant | 0.13 |
embR | 1416517 | c.831C>T | synonymous_variant | 0.18 |
embR | 1416960 | p.Arg130Trp | missense_variant | 0.18 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
inhA | 1673643 | c.-559C>T | upstream_gene_variant | 0.12 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
inhA | 1674690 | c.489C>G | synonymous_variant | 0.12 |
inhA | 1674769 | p.Ala190Thr | missense_variant | 0.13 |
rpsA | 1833387 | c.-155G>A | upstream_gene_variant | 0.15 |
rpsA | 1833975 | p.Arg145His | missense_variant | 0.12 |
rpsA | 1834922 | p.Gly461Ser | missense_variant | 0.2 |
tlyA | 1917834 | c.-106A>G | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918177 | p.Ala80Thr | missense_variant | 0.4 |
ndh | 2102149 | c.894C>T | synonymous_variant | 0.25 |
ndh | 2102257 | c.786C>T | synonymous_variant | 0.4 |
ndh | 2102449 | c.594G>A | synonymous_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155304 | p.His270Tyr | missense_variant | 0.17 |
katG | 2155744 | p.Gly123Ala | missense_variant | 1.0 |
katG | 2156362 | c.-251C>T | upstream_gene_variant | 0.15 |
katG | 2156365 | c.-254C>T | upstream_gene_variant | 0.15 |
katG | 2156408 | c.-297C>T | upstream_gene_variant | 0.18 |
katG | 2156422 | c.-311C>T | upstream_gene_variant | 0.17 |
katG | 2156427 | c.-316G>A | upstream_gene_variant | 0.17 |
katG | 2156435 | c.-324G>A | upstream_gene_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170322 | c.291C>T | synonymous_variant | 0.12 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288708 | c.534C>T | synonymous_variant | 0.2 |
pncA | 2288774 | c.468G>C | synonymous_variant | 0.11 |
pncA | 2289216 | p.Val9Thr | missense_variant | 0.15 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518581 | p.Leu156Pro | missense_variant | 0.22 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
eis | 2714344 | p.Ala330Val | missense_variant | 0.25 |
eis | 2714777 | p.Val186Leu | missense_variant | 0.2 |
eis | 2714864 | p.Gly157Ser | missense_variant | 0.33 |
ahpC | 2726002 | c.-191G>A | upstream_gene_variant | 0.14 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746201 | c.1398C>T | synonymous_variant | 0.15 |
folC | 2747531 | p.Glu23Ala | missense_variant | 0.11 |
ribD | 2987437 | p.Gly200Glu | missense_variant | 0.14 |
ribD | 2987532 | p.Gly232Trp | missense_variant | 0.13 |
Rv2752c | 3064668 | c.1524G>A | synonymous_variant | 0.14 |
Rv2752c | 3064988 | p.Met402Val | missense_variant | 0.11 |
Rv2752c | 3065002 | p.His397Arg | missense_variant | 0.18 |
Rv2752c | 3065026 | p.Arg389Gln | missense_variant | 0.15 |
Rv2752c | 3065551 | p.Ser214Leu | missense_variant | 0.14 |
Rv2752c | 3066209 | c.-18C>T | upstream_gene_variant | 0.13 |
thyX | 3067330 | p.Val206Met | missense_variant | 0.2 |
thyX | 3067997 | c.-52T>C | upstream_gene_variant | 0.25 |
thyX | 3068026 | c.-81G>A | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086957 | c.138C>T | synonymous_variant | 0.15 |
ald | 3087230 | c.411C>G | synonymous_variant | 0.22 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449354 | p.Ser284Ile | missense_variant | 0.12 |
fprA | 3473965 | c.-42A>G | upstream_gene_variant | 0.13 |
fprA | 3473984 | c.-23G>A | upstream_gene_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474698 | p.Asp231Gly | missense_variant | 0.11 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568478 | p.Gly68Ser | missense_variant | 0.2 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
Rv3236c | 3612368 | p.Thr250Met | missense_variant | 0.2 |
Rv3236c | 3612418 | c.699C>T | synonymous_variant | 0.17 |
Rv3236c | 3612599 | p.Ala173Val | missense_variant | 0.4 |
Rv3236c | 3612619 | c.498G>A | synonymous_variant | 0.18 |
Rv3236c | 3613267 | c.-151G>A | upstream_gene_variant | 0.14 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiB | 3641184 | c.-351T>C | upstream_gene_variant | 0.17 |
fbiA | 3641368 | p.Tyr276His | missense_variant | 0.33 |
fbiB | 3641418 | c.-117C>T | upstream_gene_variant | 0.2 |
fbiA | 3641438 | p.Asp299Gly | missense_variant | 0.25 |
fbiB | 3641866 | p.Ser111Phe | missense_variant | 0.22 |
fbiB | 3642210 | p.Gly226Ser | missense_variant | 0.67 |
alr | 3841171 | p.Ala84Thr | missense_variant | 1.0 |
alr | 3841253 | c.168C>T | synonymous_variant | 0.2 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.14 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.5 |
ddn | 3987045 | p.Arg68Cys | missense_variant | 0.2 |
clpC1 | 4038233 | c.2472C>T | synonymous_variant | 0.33 |
clpC1 | 4039603 | p.Ala368Pro | missense_variant | 0.15 |
clpC1 | 4040185 | p.Phe174Leu | missense_variant | 0.12 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040898 | c.-194C>T | upstream_gene_variant | 0.12 |
embC | 4239992 | p.Ala44Thr | missense_variant | 0.13 |
embC | 4240492 | c.630G>A | synonymous_variant | 0.17 |
embC | 4240553 | p.Met231Val | missense_variant | 0.25 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241290 | c.1428C>T | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242808 | c.-425C>T | upstream_gene_variant | 0.12 |
embA | 4243372 | p.Gln47Arg | missense_variant | 0.11 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4243679 | c.447C>T | synonymous_variant | 0.15 |
embA | 4243681 | p.Ala150Asp | missense_variant | 0.15 |
embA | 4243736 | c.505delC | frameshift_variant | 0.15 |
embA | 4243744 | p.Gly171Asp | missense_variant | 0.13 |
embA | 4244398 | p.Val389Gly | missense_variant | 0.2 |
embA | 4244403 | p.Val391Ile | missense_variant | 0.2 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.4 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.44 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.39 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.39 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.35 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.32 |
embB | 4246613 | p.Gly34Arg | missense_variant | 0.2 |
embB | 4247559 | p.Trp349Leu | missense_variant | 0.13 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4249347 | p.Ala945Val | missense_variant | 0.33 |
embB | 4249359 | p.Val949Glu | missense_variant | 0.25 |
aftB | 4267718 | c.1119C>T | synonymous_variant | 0.33 |
aftB | 4267759 | p.Gly360Ser | missense_variant | 0.14 |
aftB | 4267872 | p.Gln322Leu | missense_variant | 0.25 |
aftB | 4268218 | p.Trp207Gly | missense_variant | 0.18 |
aftB | 4268257 | p.Gly194Arg | missense_variant | 0.22 |
aftB | 4268441 | c.396C>T | synonymous_variant | 0.12 |
aftB | 4268516 | c.321A>G | synonymous_variant | 0.11 |
aftB | 4268869 | c.-34delG | upstream_gene_variant | 0.22 |
aftB | 4268894 | c.-58G>A | upstream_gene_variant | 0.18 |
aftB | 4268897 | c.-61G>A | upstream_gene_variant | 0.17 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
ubiA | 4270011 | c.-178A>G | upstream_gene_variant | 0.18 |
ubiA | 4270016 | c.-183G>A | upstream_gene_variant | 0.18 |
ubiA | 4270021 | c.-188T>C | upstream_gene_variant | 0.22 |
ubiA | 4270026 | c.-193C>T | upstream_gene_variant | 0.22 |
ethA | 4326903 | p.Val191Met | missense_variant | 0.2 |
whiB6 | 4338349 | p.Arg58His | missense_variant | 0.2 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4408068 | p.Trp45Cys | missense_variant | 0.12 |
gid | 4408316 | c.-114C>T | upstream_gene_variant | 0.12 |