Run ID: SRR6650235
Sample name:
Date: 15-08-2023 07:58:17
Number of reads: 492014
Percentage reads mapped: 99.45
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | ||
Fluoroquinolones | R | gyrA p.Asp94Tyr (0.42) |
Moxifloxacin | R | gyrA p.Asp94Tyr (0.42) |
Ofloxacin | R | gyrA p.Asp94Tyr (0.42) |
Levofloxacin | R | gyrA p.Asp94Tyr (0.42) |
Ciprofloxacin | R | gyrA p.Asp94Tyr (0.42) |
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 | 0.77 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7581 | p.Asp94Tyr | missense_variant | 0.42 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.15 |
gyrB | 6912 | p.Asn558Arg | missense_variant | 0.29 |
gyrB | 6918 | p.His560Leu | missense_variant | 0.29 |
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.33 |
gyrB | 6929 | p.Ala564Pro | missense_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.17 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490979 | p.Asn66Thr | missense_variant | 0.29 |
fgd1 | 491008 | p.Thr76Pro | missense_variant | 0.29 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.36 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.23 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576689 | p.Tyr448Asp | missense_variant | 0.29 |
mshA | 576723 | p.Val459Gly | missense_variant | 0.33 |
ccsA | 619713 | c.-178C>G | upstream_gene_variant | 0.2 |
ccsA | 619835 | c.-56G>T | upstream_gene_variant | 0.2 |
ccsA | 619839 | c.-52C>G | upstream_gene_variant | 0.22 |
ccsA | 619844 | c.-47T>G | upstream_gene_variant | 0.2 |
ccsA | 619851 | c.-40A>G | upstream_gene_variant | 0.18 |
ccsA | 619870 | c.-21A>C | upstream_gene_variant | 0.17 |
ccsA | 619884 | c.-7A>G | upstream_gene_variant | 0.18 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.38 |
ccsA | 620752 | p.Arg288Gly | missense_variant | 0.25 |
ccsA | 620756 | p.Asp289Gly | missense_variant | 0.3 |
ccsA | 620761 | p.Lys291Gln | missense_variant | 0.22 |
ccsA | 620770 | p.Trp294Arg | missense_variant | 0.22 |
ccsA | 620779 | p.Val297Ile | missense_variant | 0.18 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.57 |
rpoB | 759754 | c.-53A>C | upstream_gene_variant | 0.22 |
rpoB | 759808 | c.2T>G | start_lost | 0.18 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.88 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763849 | c.480G>A | synonymous_variant | 0.25 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 0.43 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 0.43 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775643 | c.2838A>C | synonymous_variant | 0.29 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777431 | c.1050A>C | synonymous_variant | 0.22 |
mmpR5 | 779336 | p.Asp116Ala | missense_variant | 0.5 |
mmpR5 | 779348 | p.Val120Gly | missense_variant | 0.43 |
mmpR5 | 779356 | p.Arg123Gly | missense_variant | 0.5 |
mmpR5 | 779363 | p.Leu125Arg | missense_variant | 0.45 |
mmpR5 | 779371 | p.Ala128Pro | missense_variant | 0.45 |
rpsL | 781363 | c.-197T>G | upstream_gene_variant | 0.43 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800988 | c.180C>A | synonymous_variant | 0.27 |
rplC | 800997 | p.Asn63Lys | missense_variant | 0.27 |
embR | 1416816 | p.Ala178Thr | missense_variant | 0.73 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.57 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474489 | n.832T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475029 | n.1372T>G | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1673668 | p.Glu77Lys | missense_variant | 0.33 |
fabG1 | 1673690 | p.Val84Gly | missense_variant | 0.29 |
fabG1 | 1674049 | p.Gln204Lys | missense_variant | 0.15 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.36 |
inhA | 1674892 | p.Asn231Asp | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918391 | p.Val151Gly | missense_variant | 0.33 |
tlyA | 1918403 | p.Leu155Pro | missense_variant | 0.27 |
tlyA | 1918419 | p.Leu160Phe | missense_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154726 | c.1386C>A | synonymous_variant | 0.29 |
katG | 2155856 | p.Thr86Pro | missense_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.38 |
PPE35 | 2169266 | c.1347C>G | synonymous_variant | 0.22 |
PPE35 | 2169278 | c.1335T>G | synonymous_variant | 0.25 |
PPE35 | 2169285 | p.Tyr443Phe | missense_variant | 0.29 |
PPE35 | 2169293 | c.1320T>G | synonymous_variant | 0.67 |
PPE35 | 2169296 | p.Asn439Lys | missense_variant | 0.25 |
PPE35 | 2169299 | p.Asn438Lys | missense_variant | 0.38 |
PPE35 | 2169303 | p.Met437Lys | missense_variant | 0.25 |
PPE35 | 2169306 | p.Asp436Gly | missense_variant | 0.25 |
PPE35 | 2169314 | p.Asn433Lys | missense_variant | 0.25 |
PPE35 | 2169317 | c.1296C>T | synonymous_variant | 0.5 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.22 |
PPE35 | 2169854 | c.759T>G | synonymous_variant | 0.2 |
PPE35 | 2170390 | p.Trp75Gly | missense_variant | 0.25 |
PPE35 | 2170407 | p.Ala69Gly | missense_variant | 0.22 |
PPE35 | 2170422 | p.Ala64Gly | missense_variant | 0.22 |
PPE35 | 2170425 | p.Val63Gly | missense_variant | 0.2 |
PPE35 | 2170436 | c.177T>G | synonymous_variant | 0.2 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.23 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223361 | c.-197C>T | upstream_gene_variant | 0.83 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.83 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.77 |
kasA | 2518147 | c.33C>T | synonymous_variant | 0.33 |
kasA | 2518151 | p.Ser13Arg | missense_variant | 0.25 |
eis | 2715103 | p.Leu77Pro | missense_variant | 0.6 |
eis | 2715117 | c.216T>G | synonymous_variant | 0.29 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.83 |
ahpC | 2726640 | p.Thr150Pro | missense_variant | 0.2 |
folC | 2746655 | p.Ala315Gly | missense_variant | 0.9 |
folC | 2746714 | c.885T>G | synonymous_variant | 0.22 |
folC | 2746745 | p.Val285Gly | missense_variant | 0.25 |
pepQ | 2859438 | c.981T>G | synonymous_variant | 0.25 |
pepQ | 2859502 | p.Pro306Arg | missense_variant | 0.18 |
pepQ | 2859904 | p.Val172Gly | missense_variant | 0.33 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.45 |
Rv2752c | 3064677 | p.Glu505Asp | missense_variant | 0.44 |
thyX | 3068024 | c.-79A>C | upstream_gene_variant | 0.25 |
thyX | 3068031 | c.-86A>C | upstream_gene_variant | 0.27 |
thyX | 3068042 | c.-97T>C | upstream_gene_variant | 0.22 |
thyX | 3068051 | c.-106A>C | upstream_gene_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339188 | p.Thr24Asn | missense_variant | 0.15 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.38 |
fbiD | 3339279 | c.162T>G | synonymous_variant | 0.25 |
fbiD | 3339281 | p.Ser55Leu | missense_variant | 0.38 |
Rv3083 | 3449079 | p.Leu192Phe | missense_variant | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.5 |
Rv3236c | 3612113 | p.Glu335Gly | missense_variant | 0.29 |
Rv3236c | 3612752 | p.Ala122Gly | missense_variant | 0.25 |
Rv3236c | 3612772 | c.345T>G | synonymous_variant | 0.33 |
Rv3236c | 3612776 | p.Asp114Gly | missense_variant | 0.38 |
Rv3236c | 3612780 | p.Leu113Val | missense_variant | 0.25 |
Rv3236c | 3612784 | p.Leu111Phe | missense_variant | 0.25 |
Rv3236c | 3612789 | p.Leu110Val | missense_variant | 0.25 |
Rv3236c | 3612793 | c.324C>G | synonymous_variant | 0.57 |
Rv3236c | 3612800 | p.Val106Gly | missense_variant | 0.29 |
Rv3236c | 3612805 | c.312T>G | synonymous_variant | 0.38 |
fbiB | 3641817 | p.Thr95Pro | missense_variant | 0.17 |
fbiB | 3642738 | p.Ile402Phe | missense_variant | 0.17 |
fbiB | 3642744 | p.Ala404Ser | missense_variant | 0.27 |
fbiB | 3642751 | p.Asp406Ala | missense_variant | 0.36 |
fbiB | 3642753 | c.1219C>T | synonymous_variant | 0.25 |
fbiB | 3642764 | p.Asp410Glu | missense_variant | 0.14 |
alr | 3841253 | c.168C>T | synonymous_variant | 0.47 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 0.71 |
alr | 3841506 | c.-86A>C | upstream_gene_variant | 0.29 |
alr | 3841528 | c.-108A>C | upstream_gene_variant | 0.19 |
clpC1 | 4039916 | c.789T>G | synonymous_variant | 0.25 |
embC | 4239973 | c.111T>G | synonymous_variant | 0.27 |
embC | 4239995 | p.Ile45Leu | missense_variant | 0.2 |
embC | 4240001 | p.Thr47Pro | missense_variant | 0.22 |
embC | 4240006 | c.144A>C | synonymous_variant | 0.38 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.43 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.7 |
embC | 4242212 | p.Ala784Pro | missense_variant | 0.29 |
embC | 4242220 | c.2358A>C | synonymous_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.27 |
embC | 4242893 | p.Ile1011Val | missense_variant | 0.33 |
embC | 4242903 | p.Asp1014Gly | missense_variant | 0.29 |
embA | 4243361 | c.129C>T | synonymous_variant | 0.2 |
embA | 4243365 | p.Trp45Gly | missense_variant | 0.2 |
embA | 4243699 | p.Pro156Leu | missense_variant | 0.7 |
embA | 4243848 | p.Val206Met | missense_variant | 0.33 |
embA | 4243971 | p.Gly247* | stop_gained | 0.14 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.5 |
embB | 4247623 | c.1110G>C | synonymous_variant | 0.3 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.3 |
embB | 4248663 | p.Val717Gly | missense_variant | 0.27 |
embB | 4248677 | p.Met722Leu | missense_variant | 0.17 |
embB | 4248689 | p.Ile726Val | missense_variant | 0.18 |
embB | 4248725 | p.Ser738Ala | missense_variant | 0.23 |
embB | 4248728 | p.Asn739His | missense_variant | 0.18 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.2 |
ubiA | 4269848 | c.-15A>G | upstream_gene_variant | 0.21 |
ubiA | 4269856 | c.-23G>A | upstream_gene_variant | 0.2 |
ubiA | 4269864 | c.-31C>G | upstream_gene_variant | 0.4 |
ethR | 4326874 | c.-675C>T | upstream_gene_variant | 0.33 |
ethA | 4326887 | p.Asp196Gly | missense_variant | 0.25 |
ethR | 4326898 | c.-651C>G | upstream_gene_variant | 0.22 |
ethR | 4327628 | p.Leu27Arg | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407780 | c.423G>A | synonymous_variant | 0.4 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.22 |
gid | 4407955 | p.Arg83Leu | missense_variant | 0.14 |