Run ID: ERR6336753
Sample name:
Date: 02-04-2023 02:02:09
Number of reads: 1391481
Percentage reads mapped: 99.05
Strain: lineage1.2.1.2.1
Drug-resistance: RR-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 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoC | 765572 | p.Asp735Asn | missense_variant | 0.17 | rifampicin |
pncA | 2288779 | p.Val155Met | missense_variant | 0.13 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7930 | p.Ala210Gly | missense_variant | 0.11 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9287 | c.1986G>A | synonymous_variant | 0.15 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490870 | p.His30Tyr | missense_variant | 0.2 |
fgd1 | 490918 | p.His46Tyr | missense_variant | 0.4 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575344 | c.-4A>G | upstream_gene_variant | 0.1 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 575464 | c.117G>A | synonymous_variant | 0.15 |
mshA | 575863 | c.516G>A | synonymous_variant | 0.13 |
rpoB | 760889 | c.1083C>T | synonymous_variant | 0.2 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.33 |
rpoB | 761535 | p.Pro577Ser | missense_variant | 0.22 |
rpoB | 761602 | p.Ala599Val | missense_variant | 0.25 |
rpoB | 761710 | p.Val635Asp | missense_variant | 0.14 |
rpoB | 761713 | p.Val636Asp | missense_variant | 0.14 |
rpoB | 762264 | p.Gly820Ser | missense_variant | 0.13 |
rpoC | 762741 | c.-629C>T | upstream_gene_variant | 0.2 |
rpoB | 762777 | p.Asp991Asn | missense_variant | 0.25 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763682 | p.Trp105Arg | missense_variant | 0.1 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764299 | p.Met310Ile | missense_variant | 0.14 |
rpoC | 766092 | p.Gly908Ala | missense_variant | 0.4 |
rpoC | 766276 | c.2907C>G | synonymous_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777616 | p.Arg289Cys | missense_variant | 0.15 |
mmpL5 | 778437 | p.Pro15Leu | missense_variant | 0.29 |
mmpS5 | 778649 | p.Leu86Pro | missense_variant | 0.12 |
mmpR5 | 779177 | p.Ser63Ile | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781759 | p.Ile67Thr | missense_variant | 0.17 |
rplC | 801010 | p.Gly68Ser | missense_variant | 0.17 |
fbiC | 1304103 | c.1173G>A | synonymous_variant | 0.13 |
fbiC | 1304302 | p.Arg458Cys | missense_variant | 1.0 |
Rv1258c | 1406142 | c.1197_1198delGC | frameshift_variant | 0.25 |
Rv1258c | 1406311 | c.1030C>T | synonymous_variant | 0.18 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406729 | c.610_611delCG | frameshift_variant | 0.12 |
embR | 1416423 | p.Arg309Gly | missense_variant | 0.15 |
embR | 1416982 | c.366C>T | synonymous_variant | 0.29 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417028 | p.Asp107Val | missense_variant | 0.14 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673554 | p.Gly39Arg | missense_variant | 0.25 |
fabG1 | 1673560 | p.Lys41Leu | missense_variant | 0.29 |
fabG1 | 1673636 | p.Asp66Gly | missense_variant | 0.13 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
inhA | 1674403 | p.Glu68Lys | missense_variant | 0.17 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.11 |
rpsA | 1834815 | p.His425Pro | missense_variant | 0.13 |
rpsA | 1834908 | p.Ser456Trp | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102092 | c.951G>A | synonymous_variant | 0.13 |
ndh | 2102106 | p.Gly313Arg | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156376 | c.-265C>T | upstream_gene_variant | 0.13 |
katG | 2156443 | c.-332C>T | upstream_gene_variant | 0.13 |
katG | 2156484 | c.-373A>G | upstream_gene_variant | 0.11 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288734 | p.Ala170Thr | missense_variant | 0.14 |
pncA | 2289357 | c.-116G>A | upstream_gene_variant | 0.14 |
pncA | 2289845 | c.-604G>C | upstream_gene_variant | 0.11 |
pncA | 2289879 | c.-638G>T | upstream_gene_variant | 0.22 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
eis | 2714812 | p.Glu174Ala | missense_variant | 0.14 |
eis | 2715491 | c.-159G>A | upstream_gene_variant | 0.18 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746136 | c.1463G>A | splice_region_variant&stop_retained_variant | 0.15 |
pepQ | 2859914 | p.Glu169Lys | missense_variant | 0.18 |
pepQ | 2859971 | p.Ala150Thr | missense_variant | 0.13 |
pepQ | 2860221 | c.198G>T | synonymous_variant | 0.33 |
ribD | 2986691 | c.-148G>A | upstream_gene_variant | 0.14 |
ribD | 2987113 | p.Gly92Ala | missense_variant | 0.11 |
ribD | 2987338 | p.Gly167Asp | missense_variant | 0.4 |
ribD | 2987394 | p.Gly186Ser | missense_variant | 0.5 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.13 |
Rv2752c | 3064822 | p.Val457Ala | missense_variant | 0.17 |
Rv2752c | 3064825 | p.Asp456Val | missense_variant | 0.17 |
Rv2752c | 3064828 | p.Gly455Asp | missense_variant | 0.2 |
Rv2752c | 3065622 | c.570G>A | synonymous_variant | 0.17 |
thyX | 3067441 | p.Gln169Lys | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087761 | c.942C>T | synonymous_variant | 0.15 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449126 | p.Thr208Met | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474099 | c.93C>T | synonymous_variant | 0.2 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.98 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.29 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
Rv3236c | 3612578 | p.Glu180Val | missense_variant | 0.15 |
Rv3236c | 3612682 | c.435C>T | synonymous_variant | 0.14 |
Rv3236c | 3612809 | p.Pro103Leu | missense_variant | 0.12 |
Rv3236c | 3612818 | c.297_298delCA | frameshift_variant | 0.14 |
Rv3236c | 3612854 | p.His88Pro | missense_variant | 0.22 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiB | 3641624 | p.Ser30Arg | missense_variant | 0.2 |
fbiB | 3642166 | p.Ala211Gly | missense_variant | 0.15 |
alr | 3840443 | c.978G>A | synonymous_variant | 0.22 |
alr | 3841104 | p.Thr106Ile | missense_variant | 0.13 |
rpoA | 3877631 | p.Ser293Thr | missense_variant | 0.12 |
rpoA | 3877748 | c.760C>T | synonymous_variant | 0.2 |
rpoA | 3877896 | c.612G>A | synonymous_variant | 0.2 |
clpC1 | 4038851 | c.1854G>A | synonymous_variant | 0.14 |
clpC1 | 4038887 | c.1818G>A | synonymous_variant | 0.2 |
clpC1 | 4038914 | c.1791G>A | synonymous_variant | 0.2 |
clpC1 | 4039048 | p.Gly553Ser | missense_variant | 0.17 |
clpC1 | 4039746 | p.Ile320Ser | missense_variant | 0.17 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.11 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.1 |
clpC1 | 4040181 | p.Gly175Asp | missense_variant | 0.17 |
clpC1 | 4040183 | c.522C>T | synonymous_variant | 0.14 |
clpC1 | 4040257 | p.Ala150Thr | missense_variant | 0.22 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240481 | p.Pro207Ser | missense_variant | 0.15 |
embC | 4240571 | p.Gly237Trp | missense_variant | 0.14 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240962 | p.Leu367Pro | missense_variant | 0.14 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242175 | c.2313G>C | synonymous_variant | 0.22 |
embC | 4242525 | p.Ala888Val | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4243939 | p.Trp236* | stop_gained | 0.2 |
embA | 4243941 | p.Leu237Met | missense_variant | 0.18 |
embA | 4244184 | p.Ser318Arg | missense_variant | 0.14 |
embA | 4244194 | p.Gly321Ala | missense_variant | 0.2 |
embA | 4244350 | p.Leu373Pro | missense_variant | 0.12 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4245427 | p.Ser732Thr | missense_variant | 0.13 |
embA | 4245829 | p.Arg866Pro | missense_variant | 0.25 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.42 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.41 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.38 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.3 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.29 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.17 |
embB | 4247244 | p.Gly244Glu | missense_variant | 0.13 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247704 | c.1191G>A | synonymous_variant | 0.12 |
embB | 4248323 | p.Ala604Thr | missense_variant | 0.18 |
embB | 4248745 | c.2232C>G | synonymous_variant | 0.14 |
embB | 4249384 | c.2871G>A | synonymous_variant | 0.67 |
aftB | 4267454 | c.1383C>T | synonymous_variant | 0.25 |
aftB | 4267736 | c.1101C>T | synonymous_variant | 0.12 |
aftB | 4268020 | p.Ser273Pro | missense_variant | 0.12 |
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 |
ethA | 4326764 | p.Ala237Val | missense_variant | 0.18 |
ethA | 4326777 | p.Met233Leu | missense_variant | 0.12 |
ethR | 4327583 | p.Pro12Leu | missense_variant | 0.15 |
ethR | 4327630 | p.Ala28Thr | missense_variant | 0.13 |
ethR | 4327994 | p.Thr149Met | missense_variant | 0.12 |
ethA | 4328385 | c.-912G>A | upstream_gene_variant | 0.12 |
whiB6 | 4338239 | c.283C>T | synonymous_variant | 0.2 |
whiB6 | 4338289 | p.Gly78Glu | missense_variant | 0.33 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338599 | c.-78A>C | 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 | 4407624 | c.579G>C | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |