Run ID: SRR6650106
Sample name:
Date: 15-08-2023 08:19:47
Number of reads: 961235
Percentage reads mapped: 99.4
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | ||
Fluoroquinolones | R | gyrA p.Asp94Gly (1.00) |
Moxifloxacin | R | gyrA p.Asp94Gly (1.00) |
Ofloxacin | R | gyrA p.Asp94Gly (1.00) |
Levofloxacin | R | gyrA p.Asp94Gly (1.00) |
Ciprofloxacin | R | gyrA p.Asp94Gly (1.00) |
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | ||
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6654 | p.Asp472Gly | missense_variant | 0.17 |
gyrA | 6898 | c.-404G>C | upstream_gene_variant | 0.2 |
gyrA | 6910 | c.-392G>A | upstream_gene_variant | 0.18 |
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.18 |
gyrB | 6927 | p.Leu563Trp | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8044 | p.Arg248Pro | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490975 | p.Thr65Pro | missense_variant | 0.25 |
fgd1 | 491008 | p.Thr76Pro | missense_variant | 0.33 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.44 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.3 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576705 | p.Gln453Pro | missense_variant | 0.18 |
mshA | 576723 | p.Val459Gly | missense_variant | 0.3 |
ccsA | 619707 | c.-184T>G | upstream_gene_variant | 0.23 |
ccsA | 620532 | c.642T>G | synonymous_variant | 0.23 |
ccsA | 620537 | p.Val216Gly | missense_variant | 0.18 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.19 |
ccsA | 620752 | p.Arg288Gly | missense_variant | 0.17 |
ccsA | 620756 | p.Asp289Gly | missense_variant | 0.24 |
rpoB | 759611 | c.-196G>C | upstream_gene_variant | 0.17 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.2 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.2 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763849 | c.480G>A | synonymous_variant | 0.17 |
rpoC | 766900 | c.3531T>G | synonymous_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781531 | c.-29T>G | upstream_gene_variant | 0.15 |
rplC | 801274 | p.Thr156Pro | missense_variant | 0.21 |
rplC | 801279 | c.471G>C | synonymous_variant | 0.19 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.29 |
rplC | 801316 | p.Met170Val | missense_variant | 0.19 |
fbiC | 1302903 | c.-28T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.25 |
atpE | 1461087 | p.Leu15Val | missense_variant | 0.2 |
atpE | 1461108 | p.Ile22Leu | missense_variant | 0.2 |
atpE | 1461131 | c.87T>G | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673679 | c.-523T>G | upstream_gene_variant | 0.18 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.27 |
ndh | 2103235 | c.-193C>G | upstream_gene_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169317 | c.1296C>T | synonymous_variant | 0.16 |
PPE35 | 2170066 | p.Ala183Pro | missense_variant | 0.27 |
PPE35 | 2170072 | p.Gly181Arg | missense_variant | 0.15 |
PPE35 | 2170383 | p.Ala77Gly | missense_variant | 0.17 |
PPE35 | 2170390 | p.Trp75Gly | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
eis | 2715032 | p.Cys101Gly | missense_variant | 0.15 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726265 | p.Lys25Gln | missense_variant | 0.15 |
ahpC | 2726277 | p.Lys29Gln | missense_variant | 0.21 |
ahpC | 2726286 | p.Gly32Arg | missense_variant | 0.21 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.15 |
pepQ | 2859358 | p.Thr354Asn | missense_variant | 0.15 |
pepQ | 2859377 | p.Thr348Ala | missense_variant | 0.18 |
pepQ | 2859414 | c.1005T>G | synonymous_variant | 0.22 |
pepQ | 2859421 | p.Arg333Pro | missense_variant | 0.2 |
pepQ | 2859454 | p.Val322Gly | missense_variant | 0.25 |
ribD | 2987323 | p.Val162Gly | missense_variant | 0.21 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.18 |
fbiD | 3339626 | p.His170Pro | missense_variant | 0.33 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612835 | c.282T>G | synonymous_variant | 0.25 |
fbiB | 3641633 | c.99C>G | synonymous_variant | 0.14 |
alr | 3841349 | c.72C>T | synonymous_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243264 | p.Arg11Gln | missense_variant | 0.94 |
embA | 4243372 | p.Gln47Arg | missense_variant | 0.15 |
embA | 4243398 | p.Thr56Pro | missense_variant | 0.18 |
embA | 4246365 | p.Tyr1045Asp | missense_variant | 0.12 |
embB | 4247616 | p.Glu368Gly | missense_variant | 0.24 |
embB | 4249403 | p.Thr964Pro | missense_variant | 0.15 |
ubiA | 4269455 | p.Val127Leu | missense_variant | 0.12 |
ubiA | 4269848 | c.-15A>G | upstream_gene_variant | 0.19 |
ethA | 4326905 | p.Leu190Pro | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |