Run ID: ERR6336761
Sample name:
Date: 02-04-2023 02:02:22
Number of reads: 721471
Percentage reads mapped: 99.09
Strain: lineage1.2.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 0.99 |
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 |
---|---|---|---|---|---|
embB | 4247583 | p.Ala357Val | missense_variant | 0.25 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 7158 | c.1931_1933dupCCG | disruptive_inframe_insertion | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7575 | p.Ile92Val | missense_variant | 0.25 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8745 | p.Glu482Lys | missense_variant | 0.25 |
gyrA | 9055 | p.Pro585Leu | missense_variant | 0.12 |
gyrA | 9063 | c.1765delC | frameshift_variant | 0.2 |
gyrA | 9076 | p.Arg592Pro | missense_variant | 0.2 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9336 | p.Gln679* | stop_gained | 0.14 |
fgd1 | 490852 | p.Ala24Thr | missense_variant | 0.18 |
fgd1 | 491109 | c.327G>A | synonymous_variant | 0.33 |
fgd1 | 491172 | c.390C>T | synonymous_variant | 0.4 |
fgd1 | 491247 | c.465C>T | synonymous_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.4 |
mshA | 576450 | p.Pro368Arg | missense_variant | 0.25 |
mshA | 576766 | c.1419G>C | synonymous_variant | 0.22 |
mshA | 576772 | c.1425T>A | synonymous_variant | 0.22 |
ccsA | 620072 | p.Pro61Leu | missense_variant | 0.29 |
ccsA | 620348 | p.Gly153Glu | missense_variant | 0.22 |
rpoB | 759893 | c.87G>A | synonymous_variant | 0.12 |
rpoB | 760707 | p.Asp301Asn | missense_variant | 0.12 |
rpoB | 761073 | p.Glu423Lys | missense_variant | 0.13 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.33 |
rpoB | 761280 | p.Gly492Ser | missense_variant | 0.2 |
rpoB | 761848 | p.Cys681Tyr | missense_variant | 0.5 |
rpoB | 762813 | p.Met1003Leu | missense_variant | 0.33 |
rpoC | 762848 | c.-522G>A | upstream_gene_variant | 0.25 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.2 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764068 | c.699G>A | synonymous_variant | 0.12 |
rpoC | 764526 | p.Arg386His | missense_variant | 0.14 |
rpoC | 765374 | p.Gly669Ser | missense_variant | 0.13 |
rpoC | 765683 | p.Glu772Lys | missense_variant | 0.14 |
rpoC | 766074 | p.Ala902Val | missense_variant | 0.2 |
rpoC | 766292 | p.Cys975Arg | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777671 | c.810G>A | synonymous_variant | 0.18 |
mmpR5 | 778037 | c.-953G>A | upstream_gene_variant | 0.17 |
mmpL5 | 778131 | p.Gln117Arg | missense_variant | 0.12 |
mmpR5 | 778223 | c.-767G>A | upstream_gene_variant | 0.12 |
mmpS5 | 778574 | p.Ser111Phe | missense_variant | 0.13 |
mmpL5 | 779178 | c.-698G>A | upstream_gene_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801160 | p.Ser118Pro | missense_variant | 0.12 |
fbiC | 1302763 | c.-168G>A | upstream_gene_variant | 0.13 |
fbiC | 1302995 | p.Asn22Ile | missense_variant | 0.12 |
fbiC | 1303490 | p.Leu187Pro | missense_variant | 0.33 |
fbiC | 1304183 | p.Ala418Glu | missense_variant | 0.2 |
fbiC | 1304675 | p.Gly582Glu | missense_variant | 0.15 |
fbiC | 1304679 | c.1749G>A | synonymous_variant | 0.15 |
fbiC | 1304892 | c.1962C>T | synonymous_variant | 0.2 |
fbiC | 1304931 | c.2001C>T | synonymous_variant | 0.13 |
fbiC | 1305248 | p.Ala773Val | missense_variant | 0.13 |
Rv1258c | 1406117 | c.1224A>G | synonymous_variant | 0.29 |
Rv1258c | 1406227 | p.Asp372Asn | missense_variant | 0.33 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406539 | p.Ala268Thr | missense_variant | 0.17 |
embR | 1416751 | p.Phe199Leu | missense_variant | 0.12 |
embR | 1416905 | p.Pro148Leu | missense_variant | 0.17 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
atpE | 1461169 | p.Gln42Arg | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
inhA | 1674388 | p.Leu63Phe | missense_variant | 0.29 |
inhA | 1674816 | c.615T>C | synonymous_variant | 0.33 |
rpsA | 1834388 | p.Pro283Ser | missense_variant | 0.17 |
rpsA | 1834392 | p.Trp284Leu | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918399 | p.Asp154His | missense_variant | 0.22 |
tlyA | 1918415 | p.Ser159Leu | missense_variant | 0.29 |
ndh | 2103227 | c.-185T>C | upstream_gene_variant | 0.25 |
katG | 2153901 | p.Phe737Leu | missense_variant | 0.17 |
katG | 2154012 | c.2100C>T | synonymous_variant | 0.18 |
katG | 2154281 | p.Leu611Phe | missense_variant | 0.13 |
katG | 2154284 | c.1828C>T | synonymous_variant | 0.13 |
katG | 2154346 | p.Pro589Leu | missense_variant | 0.12 |
katG | 2154538 | p.Gln525Arg | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154822 | c.1290G>A | synonymous_variant | 0.12 |
katG | 2155884 | c.228G>A | synonymous_variant | 0.25 |
katG | 2155914 | c.198G>A | synonymous_variant | 0.18 |
katG | 2156337 | c.-226G>A | upstream_gene_variant | 0.29 |
katG | 2156386 | c.-275G>A | upstream_gene_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.18 |
PPE35 | 2170210 | p.Ala135Thr | missense_variant | 0.14 |
Rv1979c | 2222051 | c.1114C>T | synonymous_variant | 0.14 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222366 | p.Tyr267His | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288857 | p.Asp129Asn | missense_variant | 0.12 |
pncA | 2289008 | c.234C>T | synonymous_variant | 0.13 |
pncA | 2289272 | c.-31C>T | upstream_gene_variant | 0.33 |
pncA | 2289534 | c.-293G>A | upstream_gene_variant | 0.15 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518323 | p.Ser70Asn | missense_variant | 0.12 |
kasA | 2518531 | c.417G>A | synonymous_variant | 0.12 |
kasA | 2518841 | p.Gly243Ser | missense_variant | 0.4 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
kasA | 2519306 | p.Val398Ile | missense_variant | 0.22 |
eis | 2714197 | p.Asp379Gly | missense_variant | 0.12 |
eis | 2714209 | p.Leu375Ser | missense_variant | 0.14 |
eis | 2714949 | c.384G>A | synonymous_variant | 1.0 |
ahpC | 2726027 | c.-166C>T | upstream_gene_variant | 0.13 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
folC | 2746324 | c.1275C>T | synonymous_variant | 0.5 |
pepQ | 2859415 | p.Gly335Asp | missense_variant | 0.15 |
pepQ | 2859794 | p.Asp209Asn | missense_variant | 0.14 |
pepQ | 2859857 | p.Val188Met | missense_variant | 0.18 |
ribD | 2986740 | c.-99A>G | upstream_gene_variant | 0.25 |
ribD | 2987573 | c.735C>T | synonymous_variant | 0.17 |
ribD | 2987612 | c.774C>T | synonymous_variant | 0.17 |
Rv2752c | 3064822 | p.Val457Ala | missense_variant | 0.29 |
Rv2752c | 3064828 | p.Gly455Asp | missense_variant | 0.29 |
Rv2752c | 3065067 | c.1125C>T | synonymous_variant | 0.12 |
Rv2752c | 3065485 | p.Ala236Val | missense_variant | 0.25 |
Rv2752c | 3065663 | p.Pro177Ser | missense_variant | 0.12 |
thyA | 3073866 | c.606C>T | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087293 | c.474G>T | synonymous_variant | 0.29 |
ald | 3087330 | p.Val171Ile | missense_variant | 0.33 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.45 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449441 | p.Ala313Val | missense_variant | 0.12 |
Rv3083 | 3449779 | p.Ala426Thr | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474015 | c.9C>T | synonymous_variant | 0.29 |
fprA | 3474082 | p.Ala26Thr | missense_variant | 0.29 |
fprA | 3474377 | p.Ala124Val | missense_variant | 0.13 |
fprA | 3474389 | p.Phe128Ser | missense_variant | 0.11 |
fprA | 3474526 | p.Ala174Thr | missense_variant | 0.17 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474901 | p.Ser299Arg | missense_variant | 0.4 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
whiB7 | 3568524 | c.156C>T | synonymous_variant | 0.12 |
Rv3236c | 3612432 | p.Val229Met | missense_variant | 0.12 |
Rv3236c | 3612682 | c.435C>T | synonymous_variant | 0.5 |
Rv3236c | 3612716 | p.Ala134Val | missense_variant | 0.14 |
Rv3236c | 3612772 | c.345T>A | synonymous_variant | 0.14 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiA | 3640724 | p.Asp61Val | missense_variant | 0.22 |
fbiA | 3640804 | p.Ala88Ser | missense_variant | 0.13 |
fbiA | 3640948 | p.Trp136Arg | missense_variant | 0.25 |
fbiA | 3640972 | p.Pro144Ser | missense_variant | 0.13 |
fbiB | 3641397 | c.-138G>A | upstream_gene_variant | 0.18 |
fbiB | 3641469 | c.-66G>A | upstream_gene_variant | 0.12 |
fbiB | 3642028 | p.Val165Gly | missense_variant | 0.4 |
fbiB | 3642687 | c.1153C>T | synonymous_variant | 0.13 |
alr | 3840397 | p.Cys342Arg | missense_variant | 0.14 |
rpoA | 3877737 | c.771G>A | synonymous_variant | 0.18 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.12 |
rpoA | 3878649 | c.-142T>A | upstream_gene_variant | 0.25 |
clpC1 | 4038822 | p.Glu628Gly | missense_variant | 0.11 |
clpC1 | 4038999 | p.Phe569Tyr | missense_variant | 0.13 |
clpC1 | 4040089 | p.Arg206Trp | missense_variant | 0.13 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 0.29 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
panD | 4044158 | p.Glu42Lys | missense_variant | 0.14 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4240953 | p.Ile364Thr | missense_variant | 0.13 |
embC | 4240992 | p.Ala377Val | missense_variant | 0.4 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241683 | c.1821G>A | synonymous_variant | 0.2 |
embC | 4241701 | p.Met613Ile | missense_variant | 0.17 |
embC | 4242128 | c.2266C>T | synonymous_variant | 0.17 |
embA | 4242265 | c.-968A>G | upstream_gene_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4243607 | c.375G>A | synonymous_variant | 0.2 |
embA | 4243681 | p.Ala150Val | missense_variant | 0.2 |
embA | 4244084 | c.852C>T | synonymous_variant | 0.15 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4244889 | p.Ile553Phe | missense_variant | 0.4 |
embB | 4245686 | c.-828G>C | upstream_gene_variant | 0.4 |
embA | 4245750 | p.Met840Val | missense_variant | 0.15 |
embB | 4245908 | c.-606G>A | upstream_gene_variant | 0.18 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embA | 4246194 | p.Pro988Ser | missense_variant | 0.14 |
embA | 4246311 | p.Gly1027Ser | missense_variant | 0.17 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.17 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.18 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.22 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.22 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.36 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.33 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4247667 | p.Trp385* | stop_gained | 0.67 |
embB | 4247973 | p.Thr487Ile | missense_variant | 0.14 |
embB | 4248747 | p.Gly745Val | missense_variant | 0.25 |
embB | 4248752 | p.Cys747Arg | missense_variant | 0.25 |
embB | 4248857 | p.Gly782Arg | missense_variant | 0.33 |
embB | 4248872 | p.Gly787Ser | missense_variant | 0.18 |
embB | 4248919 | c.2406C>T | synonymous_variant | 0.2 |
embB | 4249617 | p.Gly1035Asp | missense_variant | 0.13 |
embB | 4249687 | c.3174C>T | synonymous_variant | 0.18 |
aftB | 4267172 | c.1665C>T | synonymous_variant | 0.13 |
aftB | 4267393 | p.Pro482Ser | missense_variant | 0.25 |
aftB | 4267401 | p.Ala479Gly | missense_variant | 0.29 |
aftB | 4267517 | c.1320A>G | synonymous_variant | 0.17 |
aftB | 4268089 | p.Trp250Arg | missense_variant | 0.11 |
aftB | 4268148 | p.Gly230Val | missense_variant | 0.18 |
aftB | 4268703 | p.Asn45Ile | missense_variant | 0.12 |
ubiA | 4268944 | c.889delG | frameshift_variant | 0.15 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269641 | p.Ala65Thr | missense_variant | 0.2 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
ubiA | 4269875 | c.-42G>A | upstream_gene_variant | 0.18 |
ethA | 4326108 | p.Arg456Cys | missense_variant | 0.12 |
ethA | 4327608 | c.-135C>T | upstream_gene_variant | 0.22 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338440 | p.Glu28Lys | missense_variant | 0.14 |
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 | 4407808 | p.Asp132Gly | missense_variant | 0.18 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4407945 | c.258C>T | synonymous_variant | 0.2 |