Run ID: SRR6650299
Sample name:
Date: 15-08-2023 08:22:05
Number of reads: 1423973
Percentage reads mapped: 99.35
Strain: lineage1.1.3.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | R | pncA p.Ser18* (1.00) |
Streptomycin | ||
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | ||
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 1.0 |
lineage1.1.3.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289189 | p.Ser18* | stop_gained | 1.0 | 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 | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9629 | c.2328C>T | synonymous_variant | 1.0 |
fgd1 | 490979 | p.Asn66Thr | missense_variant | 0.27 |
fgd1 | 491008 | p.Thr76Pro | missense_variant | 0.31 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.36 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.34 |
fgd1 | 491661 | c.879C>G | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575852 | p.Trp169Gly | missense_variant | 0.15 |
mshA | 575856 | p.Ala170Gly | missense_variant | 0.16 |
mshA | 575873 | p.Thr176Pro | missense_variant | 0.22 |
mshA | 575886 | p.Leu180Arg | missense_variant | 0.17 |
mshA | 575926 | c.579A>C | synonymous_variant | 0.17 |
mshA | 576723 | p.Val459Gly | missense_variant | 0.4 |
ccsA | 619707 | c.-184T>G | upstream_gene_variant | 0.22 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.19 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.21 |
ccsA | 620770 | p.Trp294Arg | missense_variant | 0.14 |
rpoB | 759610 | c.-197T>C | upstream_gene_variant | 0.2 |
rpoB | 759611 | c.-196G>C | upstream_gene_variant | 0.27 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.27 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.19 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777427 | p.Thr352Pro | missense_variant | 0.19 |
mmpL5 | 777572 | c.909C>T | synonymous_variant | 1.0 |
mmpR5 | 778226 | c.-764T>C | upstream_gene_variant | 0.19 |
mmpL5 | 778239 | p.Val81Gly | missense_variant | 0.19 |
mmpL5 | 778252 | p.His77Asn | missense_variant | 0.17 |
mmpL5 | 778907 | c.-427C>G | upstream_gene_variant | 0.16 |
mmpR5 | 779336 | p.Asp116Ala | missense_variant | 0.29 |
mmpR5 | 779346 | p.Asp119Glu | missense_variant | 0.18 |
mmpR5 | 779348 | p.Val120Gly | missense_variant | 0.22 |
mmpR5 | 779362 | p.Leu125Gly | missense_variant | 0.18 |
mmpR5 | 779371 | p.Ala128Pro | missense_variant | 0.22 |
rpsL | 781363 | c.-197T>G | upstream_gene_variant | 0.3 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781524 | c.-36C>A | upstream_gene_variant | 0.21 |
rpsL | 781526 | c.-34G>A | upstream_gene_variant | 0.14 |
rpsL | 781536 | c.-24G>A | upstream_gene_variant | 0.16 |
rplC | 800981 | p.Ser58Thr | missense_variant | 0.19 |
rplC | 800988 | c.180C>A | synonymous_variant | 0.15 |
rplC | 800997 | p.Asn63Lys | missense_variant | 0.28 |
rplC | 801019 | p.Thr71Pro | missense_variant | 0.18 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.36 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.24 |
fbiC | 1303023 | c.93A>G | synonymous_variant | 0.31 |
fbiC | 1304438 | p.Glu503Gly | missense_variant | 0.2 |
Rv1258c | 1406452 | p.Thr297Pro | missense_variant | 0.2 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1461086 | c.42A>G | synonymous_variant | 0.21 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473921 | n.264A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473923 | n.266C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473932 | n.275C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473948 | n.291C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473953 | n.296T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473959 | n.302T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473973 | n.316T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474489 | n.832T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475029 | n.1372T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475066 | n.1409C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476176 | n.2519C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476200 | n.2543A>G | non_coding_transcript_exon_variant | 0.18 |
fabG1 | 1673668 | p.Glu77Lys | missense_variant | 0.14 |
inhA | 1673679 | c.-523T>G | upstream_gene_variant | 0.23 |
fabG1 | 1673690 | p.Val84Gly | missense_variant | 0.22 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.23 |
tlyA | 1917805 | c.-135C>T | upstream_gene_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918044 | p.Asp35Glu | missense_variant | 0.15 |
tlyA | 1918052 | p.Pro38Arg | missense_variant | 0.21 |
tlyA | 1918061 | p.Lys41Thr | missense_variant | 0.15 |
tlyA | 1918066 | p.Ala43Pro | missense_variant | 0.2 |
tlyA | 1918410 | c.471C>T | synonymous_variant | 0.17 |
ndh | 2103222 | c.-180A>C | upstream_gene_variant | 0.19 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.21 |
ndh | 2103235 | c.-193C>G | upstream_gene_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155856 | p.Thr86Pro | missense_variant | 0.31 |
PPE35 | 2167859 | c.2754T>G | synonymous_variant | 0.26 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>G | synonymous_variant | 0.2 |
PPE35 | 2169285 | p.Tyr443Phe | missense_variant | 0.24 |
PPE35 | 2169293 | c.1320T>G | synonymous_variant | 0.2 |
PPE35 | 2169299 | p.Asn438Lys | missense_variant | 0.2 |
PPE35 | 2169308 | c.1305C>G | synonymous_variant | 0.27 |
PPE35 | 2169317 | c.1296C>T | synonymous_variant | 0.33 |
PPE35 | 2169854 | c.759T>G | synonymous_variant | 0.17 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289386 | c.-145A>C | upstream_gene_variant | 0.17 |
pncA | 2289900 | c.-659A>C | upstream_gene_variant | 0.15 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518147 | c.33C>T | synonymous_variant | 0.4 |
kasA | 2518151 | p.Ser13Arg | missense_variant | 0.4 |
kasA | 2518605 | p.Val164Gly | missense_variant | 0.36 |
eis | 2715560 | c.-228T>G | upstream_gene_variant | 0.19 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
pepQ | 2859377 | p.Thr348Ala | missense_variant | 0.33 |
pepQ | 2859438 | c.981T>G | synonymous_variant | 0.19 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.96 |
Rv2752c | 3064745 | p.Thr483Pro | missense_variant | 0.18 |
thyX | 3068042 | c.-97T>C | upstream_gene_variant | 0.32 |
thyA | 3073811 | p.Ser221Gly | missense_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087909 | p.Thr364Pro | missense_variant | 0.2 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.37 |
fbiD | 3339279 | c.162T>G | synonymous_variant | 0.25 |
fbiD | 3339289 | p.Ser58Pro | missense_variant | 0.15 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.18 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448819 | p.Thr106Pro | missense_variant | 0.2 |
Rv3083 | 3449079 | p.Leu192Phe | missense_variant | 0.29 |
Rv3083 | 3449083 | p.Pro194Ser | missense_variant | 0.17 |
Rv3083 | 3449107 | p.Gly202Arg | missense_variant | 0.19 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3611974 | c.1143A>C | synonymous_variant | 0.2 |
Rv3236c | 3612835 | c.282T>G | synonymous_variant | 0.22 |
fbiB | 3642740 | c.1206C>T | synonymous_variant | 0.22 |
fbiB | 3642744 | p.Ala404Ser | missense_variant | 0.29 |
fbiB | 3642751 | p.Asp406Ala | missense_variant | 0.26 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.37 |
alr | 3841253 | c.168C>T | synonymous_variant | 0.97 |
alr | 3841277 | c.144C>T | synonymous_variant | 0.97 |
alr | 3841506 | c.-86A>C | upstream_gene_variant | 0.23 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4239973 | c.111T>G | synonymous_variant | 0.33 |
embC | 4240001 | p.Thr47Pro | missense_variant | 0.18 |
embC | 4240006 | c.144A>C | synonymous_variant | 0.19 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242220 | c.2358A>C | synonymous_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243350 | p.Thr40Pro | missense_variant | 0.19 |
embA | 4243372 | p.Gln47Arg | missense_variant | 0.18 |
embA | 4243380 | p.Thr50Pro | missense_variant | 0.17 |
embA | 4243398 | p.Thr56Pro | missense_variant | 0.23 |
embA | 4243848 | p.Val206Met | missense_variant | 1.0 |
embA | 4243930 | p.Leu233Pro | missense_variant | 0.16 |
embA | 4244748 | p.Thr506Pro | missense_variant | 0.23 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247623 | c.1110G>C | synonymous_variant | 0.22 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249403 | p.Thr964Pro | missense_variant | 0.2 |
aftB | 4268758 | p.Ile27Val | missense_variant | 0.2 |
aftB | 4268776 | p.Ser21Gly | missense_variant | 0.18 |
aftB | 4268799 | p.Val13Gly | missense_variant | 0.21 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269486 | c.-650T>G | upstream_gene_variant | 0.2 |
ubiA | 4269502 | p.Val111Gly | missense_variant | 0.19 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269848 | c.-15A>G | upstream_gene_variant | 0.23 |
ubiA | 4269864 | c.-31C>G | upstream_gene_variant | 0.24 |
ethA | 4326887 | p.Asp196Gly | missense_variant | 0.21 |
ethA | 4326905 | p.Leu190Pro | missense_variant | 0.17 |
ethR | 4327597 | p.Thr17Pro | missense_variant | 0.2 |
ethR | 4327624 | p.Glu26Lys | missense_variant | 0.18 |
ethR | 4327642 | p.Thr32Pro | missense_variant | 0.42 |
ethR | 4327768 | p.Thr74Pro | missense_variant | 0.18 |
ethR | 4327813 | p.Thr89Pro | missense_variant | 0.23 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407780 | c.423G>A | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
whiB6 | 4338429 | c.-218_92del | frameshift_variant&start_lost | 1.0 |