Run ID: ERR1949994
Sample name:
Date: 31-03-2023 15:36:52
Number of reads: 284811
Percentage reads mapped: 99.13
Strain: lineage4
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761136 | p.Thr444Pro | missense_variant | 0.67 | rifampicin |
rpoB | 761154 | p.Ser450Ala | missense_variant | 0.5 | rifampicin |
katG | 2155859 | p.Thr85Pro | missense_variant | 0.67 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5086 | c.-154A>C | upstream_gene_variant | 0.4 |
gyrB | 5686 | c.447T>A | synonymous_variant | 0.6 |
gyrB | 6314 | p.Ser359Thr | missense_variant | 0.33 |
gyrB | 6353 | p.Lys372* | stop_gained | 0.67 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8075 | p.Glu258Asp | missense_variant | 0.4 |
gyrA | 8316 | p.Thr339Pro | missense_variant | 0.29 |
gyrA | 8404 | p.His368Leu | missense_variant | 0.33 |
gyrA | 9807 | p.Thr836Ala | missense_variant | 0.18 |
mshA | 575590 | c.243T>C | synonymous_variant | 0.33 |
mshA | 575604 | p.Val86Ala | missense_variant | 0.22 |
mshA | 575757 | p.Leu137Arg | missense_variant | 0.25 |
ccsA | 619943 | p.Phe18Ser | missense_variant | 0.22 |
ccsA | 620056 | p.Thr56Pro | missense_variant | 0.5 |
ccsA | 620117 | p.Val76Gly | missense_variant | 0.75 |
rpoB | 760770 | p.Ile322Phe | missense_variant | 0.4 |
rpoB | 761283 | p.Ser493Ala | missense_variant | 0.22 |
rpoB | 761398 | p.Asp531Ala | missense_variant | 0.4 |
rpoB | 761491 | p.Val562Gly | missense_variant | 0.33 |
rpoC | 763532 | p.Thr55Pro | missense_variant | 0.5 |
rpoC | 766283 | p.Thr972Ala | missense_variant | 0.33 |
rpoC | 766301 | p.Cys978Ser | missense_variant | 0.29 |
rpoC | 766442 | p.Thr1025Pro | missense_variant | 0.25 |
rpoC | 766712 | p.Ser1115Ala | missense_variant | 0.25 |
rpoC | 766865 | p.Thr1166Pro | missense_variant | 0.43 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775677 | p.Lys935Met | missense_variant | 0.4 |
mmpL5 | 777354 | p.Val376Gly | missense_variant | 0.22 |
mmpL5 | 777378 | p.Leu368Arg | missense_variant | 0.27 |
mmpL5 | 778011 | p.Gln157Leu | missense_variant | 0.29 |
mmpR5 | 778034 | c.-956A>T | upstream_gene_variant | 0.29 |
mmpL5 | 778078 | p.Thr135Pro | missense_variant | 0.29 |
mmpS5 | 778566 | p.Cys114Ser | missense_variant | 0.33 |
mmpS5 | 778793 | p.Leu38* | stop_gained | 0.3 |
mmpL5 | 778816 | c.-336T>A | upstream_gene_variant | 0.25 |
rpsL | 781365 | c.-195T>A | upstream_gene_variant | 0.29 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781512 | c.-48A>T | upstream_gene_variant | 0.33 |
fbiC | 1303525 | p.Ser199Ala | missense_variant | 0.5 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304699 | p.Glu590Ala | missense_variant | 0.25 |
fbiC | 1305433 | p.Ala835Ser | missense_variant | 0.25 |
embR | 1416514 | p.Asp278Glu | missense_variant | 0.5 |
embR | 1416847 | p.Val167Gly | missense_variant | 0.29 |
embR | 1416925 | c.423A>T | synonymous_variant | 0.4 |
atpE | 1461285 | p.Lys81* | stop_gained | 0.75 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471844 | n.-2G>T | upstream_gene_variant | 0.25 |
rrs | 1471862 | n.17T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472249 | n.404T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472528 | n.683T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473170 | n.1325A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473183 | n.1338A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473824 | n.167A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474017 | n.360A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474033 | n.376A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474298 | n.641T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474927 | n.1270T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476190 | n.2533C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476335 | n.2678C>A | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1833406 | c.-136A>T | upstream_gene_variant | 0.4 |
rpsA | 1833506 | c.-36C>A | upstream_gene_variant | 0.5 |
rpsA | 1833988 | c.447C>A | synonymous_variant | 0.33 |
rpsA | 1834240 | c.699T>G | synonymous_variant | 0.22 |
rpsA | 1834308 | p.Asp256Gly | missense_variant | 0.22 |
rpsA | 1834791 | p.Arg417Leu | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101718 | p.Leu442Arg | missense_variant | 0.5 |
ndh | 2101957 | p.Phe362Leu | missense_variant | 0.4 |
katG | 2154243 | p.Glu623Asp | missense_variant | 0.67 |
katG | 2154696 | c.1416A>T | synonymous_variant | 0.4 |
katG | 2155086 | c.1026G>A | synonymous_variant | 1.0 |
katG | 2155200 | p.Tyr304* | stop_gained | 0.4 |
katG | 2155521 | p.Tyr197* | stop_gained | 0.4 |
katG | 2155945 | p.Asp56Ala | missense_variant | 0.29 |
katG | 2156343 | c.-232A>T | upstream_gene_variant | 0.67 |
PPE35 | 2168552 | c.2061T>A | synonymous_variant | 0.33 |
PPE35 | 2168596 | p.Phe673Ile | missense_variant | 0.2 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169019 | p.Leu532Met | missense_variant | 0.33 |
PPE35 | 2169104 | c.1509G>A | synonymous_variant | 0.4 |
PPE35 | 2169379 | p.Phe412Ile | missense_variant | 0.22 |
PPE35 | 2170432 | p.Ser61Ala | missense_variant | 0.4 |
Rv1979c | 2221922 | p.Lys415* | stop_gained | 0.33 |
Rv1979c | 2223013 | p.Tyr51Phe | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288862 | p.Glu127Val | missense_variant | 0.25 |
pncA | 2288865 | p.Asp126Val | missense_variant | 0.22 |
kasA | 2518314 | p.Pro67Gln | missense_variant | 0.67 |
kasA | 2518607 | p.Met165Leu | missense_variant | 0.33 |
kasA | 2518625 | p.Cys171Gly | missense_variant | 0.33 |
kasA | 2518707 | p.Val198Gly | missense_variant | 0.5 |
kasA | 2519012 | c.898T>C | synonymous_variant | 0.33 |
eis | 2714312 | p.Thr341Pro | missense_variant | 0.29 |
eis | 2714884 | p.His150Leu | missense_variant | 0.3 |
eis | 2715086 | p.Ser83Cys | missense_variant | 0.29 |
eis | 2715103 | p.Leu77Arg | missense_variant | 0.22 |
folC | 2746262 | p.Leu446Gln | missense_variant | 0.4 |
folC | 2746285 | p.Asp438Glu | missense_variant | 0.5 |
folC | 2746485 | p.Phe372Ile | missense_variant | 0.33 |
folC | 2746551 | p.Ile350Leu | missense_variant | 0.5 |
folC | 2747442 | c.157T>C | synonymous_variant | 1.0 |
folC | 2747677 | c.-79T>G | upstream_gene_variant | 0.33 |
pepQ | 2859313 | p.Leu369Gln | missense_variant | 0.29 |
pepQ | 2859834 | c.585T>G | synonymous_variant | 0.4 |
pepQ | 2860114 | p.Val102Gly | missense_variant | 0.29 |
pepQ | 2860129 | p.Phe97Cys | missense_variant | 0.33 |
ribD | 2987192 | c.354A>T | synonymous_variant | 0.29 |
ribD | 2987453 | c.615T>G | synonymous_variant | 0.5 |
Rv2752c | 3065213 | p.Thr327Ala | missense_variant | 0.33 |
Rv2752c | 3065215 | p.Ile326Ser | missense_variant | 0.4 |
Rv2752c | 3066224 | c.-33T>G | upstream_gene_variant | 0.5 |
Rv2752c | 3067041 | c.-850C>A | upstream_gene_variant | 0.5 |
thyX | 3067249 | p.Thr233Pro | missense_variant | 0.4 |
thyA | 3073777 | p.Leu232Gln | missense_variant | 0.29 |
ald | 3087183 | p.Thr122Pro | missense_variant | 0.38 |
ald | 3087825 | p.Asn336Asp | missense_variant | 0.33 |
fprA | 3473837 | c.-170A>T | upstream_gene_variant | 0.4 |
fprA | 3474059 | p.Ala18Gly | missense_variant | 0.33 |
fprA | 3475151 | p.Leu382* | stop_gained | 0.29 |
fprA | 3475163 | p.Leu386His | missense_variant | 0.29 |
whiB7 | 3568687 | c.-8A>T | upstream_gene_variant | 0.5 |
Rv3236c | 3612186 | p.Phe311Ile | missense_variant | 0.67 |
Rv3236c | 3612572 | p.Val182Gly | missense_variant | 0.22 |
Rv3236c | 3612605 | p.Val171Gly | missense_variant | 0.4 |
Rv3236c | 3612986 | p.Gly44Val | missense_variant | 0.4 |
fbiA | 3641021 | p.Val160Asp | missense_variant | 0.33 |
fbiA | 3641086 | p.Thr182Pro | missense_variant | 0.29 |
fbiA | 3641239 | p.Leu233Val | missense_variant | 0.5 |
fbiB | 3642062 | p.Tyr176* | stop_gained | 0.22 |
fbiB | 3642280 | p.Leu249Arg | missense_variant | 0.5 |
alr | 3840217 | p.Tyr402Asn | missense_variant | 0.22 |
alr | 3840408 | p.Val338Ala | missense_variant | 0.17 |
alr | 3840429 | p.Asn331Thr | missense_variant | 0.29 |
alr | 3840543 | p.Val293Gly | missense_variant | 0.25 |
alr | 3840588 | p.Lys278Ile | missense_variant | 0.36 |
alr | 3841269 | p.Val51Ala | missense_variant | 0.17 |
alr | 3841572 | c.-152T>A | upstream_gene_variant | 0.4 |
rpoA | 3878463 | c.45C>A | synonymous_variant | 0.4 |
clpC1 | 4039121 | c.1584T>G | synonymous_variant | 0.29 |
clpC1 | 4039335 | p.Leu457Gln | missense_variant | 0.22 |
clpC1 | 4039498 | p.Ile403Val | missense_variant | 0.21 |
clpC1 | 4039897 | p.Lys270Glu | missense_variant | 0.18 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.25 |
clpC1 | 4040522 | p.Ser61Arg | missense_variant | 0.5 |
clpC1 | 4040877 | c.-173T>G | upstream_gene_variant | 0.25 |
clpC1 | 4040890 | c.-186A>G | upstream_gene_variant | 0.33 |
embC | 4240017 | p.Val52Gly | missense_variant | 0.25 |
embC | 4240069 | p.Ser69Arg | missense_variant | 0.33 |
embC | 4240712 | p.Trp284Arg | missense_variant | 0.4 |
embC | 4240979 | p.Thr373Pro | missense_variant | 0.25 |
embC | 4242468 | p.Tyr869Cys | missense_variant | 0.22 |
embC | 4242479 | p.Thr873Ala | missense_variant | 0.44 |
embC | 4242486 | p.Glu875Ala | missense_variant | 0.43 |
embC | 4242602 | p.Ser914Ala | missense_variant | 0.33 |
embA | 4242625 | c.-608T>C | upstream_gene_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243138 | c.-95C>A | upstream_gene_variant | 0.22 |
embA | 4243208 | c.-25A>C | upstream_gene_variant | 0.25 |
embA | 4243398 | p.Thr56Pro | missense_variant | 0.33 |
embA | 4243849 | p.Val206Gly | missense_variant | 0.25 |
embA | 4244608 | p.Leu459Arg | missense_variant | 0.25 |
embA | 4244880 | p.Trp550Gly | missense_variant | 0.5 |
embA | 4245949 | p.Gln906Pro | missense_variant | 0.25 |
embB | 4246911 | p.Leu133* | stop_gained | 0.25 |
embB | 4247141 | p.Phe210Val | missense_variant | 0.5 |
embB | 4247219 | p.Leu236Val | missense_variant | 0.5 |
embB | 4247742 | p.Leu410Arg | missense_variant | 0.29 |
embB | 4248395 | p.Phe628Val | missense_variant | 0.44 |
embB | 4248587 | p.Gly692Ser | missense_variant | 0.29 |
aftB | 4267685 | c.1152T>G | synonymous_variant | 0.4 |
ubiA | 4269988 | c.-155T>A | upstream_gene_variant | 0.4 |
ethA | 4327083 | p.Cys131Ser | missense_variant | 0.6 |
ethA | 4327127 | p.Trp116Leu | missense_variant | 0.4 |
ethR | 4327817 | p.Leu90His | missense_variant | 0.5 |
ethR | 4328058 | p.Glu170Asp | missense_variant | 0.67 |
ethA | 4328345 | c.-872T>A | upstream_gene_variant | 0.29 |
ethA | 4328352 | c.-879T>C | upstream_gene_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407552 | c.651G>T | synonymous_variant | 0.5 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |