Run ID: SRR6650127
Sample name:
Date: 15-08-2023 07:56:13
Number of reads: 646521
Percentage reads mapped: 99.27
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
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 |
---|---|---|---|---|
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 0.98 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 1.0 |
gyrB | 5530 | c.291C>T | synonymous_variant | 1.0 |
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 | 9585 | p.Leu762Val | missense_variant | 0.25 |
fgd1 | 491008 | p.Thr76Pro | missense_variant | 0.2 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.29 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575886 | p.Leu180Arg | missense_variant | 0.2 |
mshA | 576489 | p.Val381Gly | missense_variant | 0.25 |
mshA | 576723 | p.Val459Gly | missense_variant | 0.33 |
ccsA | 619707 | c.-184T>G | upstream_gene_variant | 0.3 |
ccsA | 619738 | c.-153T>G | upstream_gene_variant | 0.25 |
ccsA | 619831 | c.-60T>G | upstream_gene_variant | 0.29 |
ccsA | 619844 | c.-47T>G | upstream_gene_variant | 0.33 |
ccsA | 620135 | p.Ala82Gly | missense_variant | 0.22 |
ccsA | 620545 | p.Leu219Val | missense_variant | 0.33 |
ccsA | 620586 | c.696C>T | synonymous_variant | 1.0 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.38 |
ccsA | 620752 | p.Arg288Gly | missense_variant | 0.29 |
ccsA | 620756 | p.Asp289Gly | missense_variant | 0.22 |
rpoB | 759792 | c.-15C>T | upstream_gene_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763849 | c.480G>A | synonymous_variant | 0.17 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764147 | p.Ser260Ala | missense_variant | 0.17 |
rpoC | 765889 | c.2520C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777155 | c.1326G>C | synonymous_variant | 1.0 |
mmpL5 | 778239 | p.Val81Gly | missense_variant | 0.2 |
mmpL5 | 778252 | p.His77Asn | missense_variant | 0.15 |
mmpS5 | 778899 | p.Gly3* | stop_gained | 0.15 |
mmpR5 | 779346 | p.Asp119Glu | missense_variant | 0.15 |
mmpR5 | 779348 | p.Val120Gly | missense_variant | 0.25 |
mmpR5 | 779356 | p.Arg123Gly | missense_variant | 0.27 |
mmpR5 | 779363 | p.Leu125Arg | missense_variant | 0.33 |
mmpR5 | 779369 | p.Asp127Ala | missense_variant | 0.2 |
mmpR5 | 779371 | p.Ala128Pro | missense_variant | 0.4 |
rpsL | 781363 | c.-197T>G | upstream_gene_variant | 0.57 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801276 | c.468G>C | synonymous_variant | 0.2 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.25 |
fbiC | 1302948 | c.18T>G | synonymous_variant | 1.0 |
Rv1258c | 1406452 | p.Thr297Pro | missense_variant | 0.43 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417480 | c.-133G>T | upstream_gene_variant | 0.67 |
atpE | 1461083 | c.39T>G | synonymous_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673668 | p.Glu77Lys | missense_variant | 0.29 |
inhA | 1673679 | c.-523T>G | upstream_gene_variant | 0.29 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.42 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918403 | p.Leu155Pro | missense_variant | 0.17 |
tlyA | 1918410 | c.471C>T | synonymous_variant | 0.27 |
tlyA | 1918431 | p.Leu164Phe | missense_variant | 0.25 |
tlyA | 1918435 | p.Ala166Pro | missense_variant | 0.15 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.18 |
ndh | 2103235 | c.-193C>G | upstream_gene_variant | 0.18 |
katG | 2153914 | p.Asn733Thr | missense_variant | 0.2 |
katG | 2153925 | p.Asp729Glu | missense_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155856 | p.Thr86Pro | missense_variant | 0.19 |
PPE35 | 2167828 | p.Ala929Pro | missense_variant | 1.0 |
PPE35 | 2167859 | c.2754T>G | synonymous_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2169285 | p.Tyr443Phe | missense_variant | 0.17 |
PPE35 | 2169317 | c.1296C>T | synonymous_variant | 0.25 |
PPE35 | 2169854 | c.759T>G | synonymous_variant | 0.3 |
PPE35 | 2169934 | p.Ile227Val | missense_variant | 1.0 |
PPE35 | 2170082 | c.531T>G | synonymous_variant | 0.18 |
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 | 0.23 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518138 | p.Asn8Lys | missense_variant | 0.17 |
eis | 2715103 | p.Leu77Pro | missense_variant | 0.21 |
eis | 2715396 | c.-64G>T | upstream_gene_variant | 0.25 |
eis | 2715411 | c.-79A>C | upstream_gene_variant | 0.2 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726269 | p.Val26Gly | missense_variant | 0.67 |
ahpC | 2726277 | p.Lys29Gln | missense_variant | 0.6 |
ahpC | 2726286 | p.Gly32Arg | missense_variant | 0.29 |
ahpC | 2726502 | p.Lys104Gln | missense_variant | 0.22 |
ahpC | 2726506 | p.Thr105Lys | missense_variant | 0.17 |
ahpC | 2726519 | c.327G>C | synonymous_variant | 0.17 |
folC | 2747753 | c.-155G>A | upstream_gene_variant | 1.0 |
pepQ | 2859377 | p.Thr348Ala | missense_variant | 0.27 |
pepQ | 2859414 | c.1005T>G | synonymous_variant | 0.18 |
pepQ | 2859425 | p.Gly332Arg | missense_variant | 0.18 |
pepQ | 2859454 | p.Val322Gly | missense_variant | 0.23 |
pepQ | 2859495 | p.Ile308Met | missense_variant | 0.15 |
pepQ | 2860068 | c.351G>A | synonymous_variant | 0.15 |
Rv2752c | 3064889 | p.Lys435Glu | missense_variant | 1.0 |
Rv2752c | 3066103 | p.Asn30Ser | missense_variant | 1.0 |
thyA | 3073829 | p.Gln215Lys | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.42 |
fbiD | 3339279 | c.162T>G | synonymous_variant | 0.31 |
fbiD | 3339281 | p.Ser55Leu | missense_variant | 0.23 |
fbiD | 3339291 | c.174G>C | synonymous_variant | 0.17 |
fbiD | 3339310 | p.Asp65His | missense_variant | 0.18 |
fbiD | 3339328 | p.Ala71Thr | missense_variant | 1.0 |
fbiD | 3339583 | p.Thr156Pro | missense_variant | 0.25 |
fbiD | 3339593 | p.His159Pro | missense_variant | 0.38 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3449079 | p.Leu192Phe | missense_variant | 0.29 |
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 |
fprA | 3475280 | p.Val425Gly | missense_variant | 0.25 |
Rv3236c | 3611974 | p.Ala381Pro | missense_variant | 0.21 |
Rv3236c | 3611988 | p.Leu377Val | missense_variant | 0.25 |
Rv3236c | 3612384 | p.Phe245Val | missense_variant | 0.22 |
Rv3236c | 3612388 | c.729T>G | synonymous_variant | 0.22 |
Rv3236c | 3612422 | p.Val232Gly | missense_variant | 0.2 |
Rv3236c | 3612541 | p.Leu192Phe | missense_variant | 0.18 |
fbiA | 3641336 | p.Val265Ala | missense_variant | 0.14 |
fbiB | 3642751 | p.Asp406Ala | missense_variant | 1.0 |
fbiB | 3642769 | p.Leu412Arg | missense_variant | 1.0 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 1.0 |
alr | 3841506 | c.-86A>C | upstream_gene_variant | 0.23 |
alr | 3841509 | c.-89A>C | upstream_gene_variant | 0.38 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 1.0 |
ddn | 3986919 | p.Thr26Pro | missense_variant | 0.23 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.5 |
clpC1 | 4038880 | p.Gln609Lys | missense_variant | 0.29 |
clpC1 | 4039916 | c.789T>G | synonymous_variant | 0.23 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4239973 | c.111T>G | synonymous_variant | 0.36 |
embC | 4240001 | p.Thr47Pro | missense_variant | 0.3 |
embC | 4240006 | c.144A>C | synonymous_variant | 0.36 |
embC | 4240008 | p.Leu49Pro | missense_variant | 0.22 |
embC | 4240017 | p.Val52Gly | missense_variant | 0.22 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4242170 | p.Thr770Pro | missense_variant | 0.25 |
embC | 4242180 | p.Leu773Trp | missense_variant | 0.29 |
embC | 4242186 | p.Asp775Ala | missense_variant | 0.29 |
embC | 4242220 | c.2358A>C | synonymous_variant | 0.4 |
embC | 4242223 | c.2361C>A | synonymous_variant | 0.33 |
embC | 4242390 | p.Leu843Arg | missense_variant | 0.15 |
embC | 4242393 | p.Asp844Ala | missense_variant | 0.18 |
embA | 4242406 | c.-827A>C | upstream_gene_variant | 0.2 |
embC | 4242414 | p.Leu851Arg | missense_variant | 0.3 |
embC | 4242422 | p.Trp854Gly | missense_variant | 0.2 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.25 |
embA | 4242901 | c.-332G>C | upstream_gene_variant | 0.18 |
embC | 4242908 | p.Phe1016Val | missense_variant | 0.18 |
embA | 4242931 | c.-302G>C | upstream_gene_variant | 0.15 |
embA | 4244653 | p.Gln474Pro | missense_variant | 0.15 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247616 | p.Glu368Gly | missense_variant | 0.21 |
embB | 4247623 | c.1110G>C | synonymous_variant | 0.27 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248799 | c.2286T>G | synonymous_variant | 0.27 |
embB | 4249305 | p.Asn931Thr | missense_variant | 0.22 |
embB | 4249314 | p.Phe934Ser | missense_variant | 0.22 |
embB | 4249322 | p.Ala937Lys | missense_variant | 0.38 |
embB | 4249330 | p.Met939Ile | missense_variant | 0.25 |
aftB | 4267637 | c.1200C>T | synonymous_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269828 | p.Ser2Arg | missense_variant | 0.33 |
ubiA | 4269833 | c.1A>G | start_lost | 0.2 |
ubiA | 4269848 | c.-15A>G | upstream_gene_variant | 0.31 |
ubiA | 4269856 | c.-23G>A | upstream_gene_variant | 0.17 |
ubiA | 4269864 | c.-31C>G | upstream_gene_variant | 0.55 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
ethA | 4326876 | p.Lys200Gln | missense_variant | 0.17 |
ethA | 4326887 | p.Asp196Gly | missense_variant | 0.42 |
ethA | 4326903 | p.Val191Leu | missense_variant | 0.21 |
ethA | 4326905 | p.Leu190Pro | missense_variant | 0.29 |
ethR | 4327624 | p.Glu26Lys | missense_variant | 0.15 |
ethR | 4327634 | p.Ile29Thr | missense_variant | 0.2 |
ethR | 4327637 | p.Leu30Pro | missense_variant | 0.33 |
ethR | 4327642 | p.Thr32Pro | missense_variant | 0.33 |
ethR | 4327813 | p.Thr89Pro | missense_variant | 0.36 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338635 | c.-114A>C | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |