Run ID: SRR6650401
Sample name:
Date: 15-08-2023 08:23:53
Number of reads: 652993
Percentage reads mapped: 99.28
Strain: lineage1.2.2.2
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 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 1.0 |
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 | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrB | 6645 | p.Ser469Asn | missense_variant | 0.18 |
gyrA | 7268 | c.-34C>T | upstream_gene_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 | 9289 | p.Val663Gly | missense_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491008 | p.Thr76Pro | missense_variant | 0.36 |
fgd1 | 491014 | p.Thr78Pro | missense_variant | 0.5 |
fgd1 | 491018 | p.Phe79Ser | missense_variant | 0.2 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.33 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576321 | p.Val325Gly | missense_variant | 0.22 |
mshA | 576723 | p.Val459Gly | missense_variant | 0.3 |
ccsA | 619835 | c.-56G>T | upstream_gene_variant | 0.25 |
ccsA | 619839 | c.-52C>G | upstream_gene_variant | 0.18 |
ccsA | 620752 | p.Arg288Gly | missense_variant | 0.22 |
ccsA | 620756 | p.Asp289Gly | missense_variant | 0.22 |
rpoB | 759795 | c.-12G>A | upstream_gene_variant | 0.18 |
rpoB | 759811 | p.Ala2Glu | missense_variant | 0.2 |
rpoB | 759816 | p.Ser4Pro | missense_variant | 0.2 |
rpoB | 762824 | p.Asp1006Glu | missense_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.86 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
mmpL5 | 775603 | p.Thr960Pro | missense_variant | 0.33 |
mmpL5 | 775625 | p.Trp952Cys | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775643 | c.2838A>C | synonymous_variant | 0.21 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777427 | p.Thr352Pro | missense_variant | 0.25 |
mmpR5 | 779336 | p.Asp116Ala | missense_variant | 0.23 |
mmpR5 | 779346 | p.Asp119Glu | missense_variant | 0.38 |
mmpR5 | 779348 | p.Val120Gly | missense_variant | 0.46 |
mmpR5 | 779354 | p.Leu122Arg | missense_variant | 0.19 |
mmpR5 | 779356 | p.Arg123Gly | missense_variant | 0.38 |
mmpR5 | 779363 | p.Leu125Arg | missense_variant | 0.38 |
mmpR5 | 779371 | p.Ala128Pro | missense_variant | 0.33 |
rpsL | 781363 | c.-197T>G | upstream_gene_variant | 0.35 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801274 | p.Thr156Pro | missense_variant | 0.29 |
rplC | 801287 | p.Val160Gly | missense_variant | 0.67 |
rplC | 801316 | p.Met170Val | missense_variant | 0.33 |
fbiC | 1303199 | p.Val90Gly | missense_variant | 0.19 |
fbiC | 1304435 | p.Ala502Gly | missense_variant | 0.25 |
fbiC | 1304438 | p.Glu503Gly | missense_variant | 0.33 |
Rv1258c | 1406452 | p.Thr297Pro | missense_variant | 0.29 |
Rv1258c | 1407075 | p.Val89Gly | missense_variant | 0.25 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473921 | n.264A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473953 | n.296T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474489 | n.832T>G | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673690 | p.Val84Gly | missense_variant | 0.2 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.55 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918029 | c.90C>A | synonymous_variant | 0.2 |
tlyA | 1918065 | c.126G>C | synonymous_variant | 0.33 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 1.0 |
PPE35 | 2169293 | c.1320T>G | synonymous_variant | 0.33 |
PPE35 | 2169299 | p.Asn438Lys | missense_variant | 0.22 |
PPE35 | 2169317 | c.1296C>T | synonymous_variant | 0.67 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.33 |
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 | 0.27 |
pncA | 2289500 | c.-259A>G | upstream_gene_variant | 0.2 |
pncA | 2289509 | c.-268A>G | upstream_gene_variant | 0.21 |
pncA | 2289511 | c.-270T>G | upstream_gene_variant | 0.42 |
pncA | 2290198 | c.-957C>T | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518147 | c.33C>T | synonymous_variant | 0.18 |
kasA | 2518151 | p.Ser13Arg | missense_variant | 0.2 |
kasA | 2518155 | p.Val14Gly | missense_variant | 0.18 |
kasA | 2518605 | p.Val164Gly | missense_variant | 0.29 |
eis | 2715396 | c.-64G>T | upstream_gene_variant | 0.2 |
eis | 2715413 | c.-81G>C | upstream_gene_variant | 0.3 |
eis | 2715560 | c.-228T>G | upstream_gene_variant | 0.17 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726265 | p.Lys25Gln | missense_variant | 0.22 |
ahpC | 2726269 | p.Val26Gly | missense_variant | 0.22 |
ahpC | 2726277 | p.Lys29Gln | missense_variant | 0.44 |
ahpC | 2726286 | p.Gly32Arg | missense_variant | 0.36 |
folC | 2746745 | p.Val285Gly | missense_variant | 0.18 |
pepQ | 2859340 | p.Glu360Gly | missense_variant | 0.23 |
pepQ | 2859367 | p.Met351Lys | missense_variant | 0.25 |
pepQ | 2859377 | p.Thr348Ala | missense_variant | 0.56 |
pepQ | 2859414 | c.1005T>G | synonymous_variant | 0.18 |
pepQ | 2859438 | c.981T>G | synonymous_variant | 0.17 |
pepQ | 2859454 | p.Val322Gly | missense_variant | 0.18 |
Rv2752c | 3066181 | p.Asp4Ala | missense_variant | 0.18 |
thyX | 3067995 | c.-50A>C | upstream_gene_variant | 0.31 |
thyX | 3068024 | c.-79A>C | upstream_gene_variant | 0.2 |
thyX | 3068031 | c.-86A>C | upstream_gene_variant | 0.2 |
thyX | 3068042 | c.-97T>C | upstream_gene_variant | 0.25 |
thyX | 3068051 | c.-106A>C | upstream_gene_variant | 0.18 |
thyA | 3073811 | p.Ser221Gly | missense_variant | 0.15 |
thyA | 3073842 | p.Asp210Glu | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087670 | p.Asp284Ala | missense_variant | 0.18 |
fbiD | 3339153 | p.Leu12Phe | missense_variant | 0.22 |
fbiD | 3339160 | p.Ala15Pro | missense_variant | 0.22 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.46 |
fbiD | 3339279 | c.162T>G | synonymous_variant | 0.46 |
fbiD | 3339292 | p.Ile59Val | missense_variant | 0.2 |
fbiD | 3339310 | p.Asp65His | missense_variant | 0.33 |
fbiD | 3339688 | p.Thr191Pro | missense_variant | 0.31 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
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 | 0.14 |
Rv3236c | 3612356 | p.Glu254Gly | missense_variant | 0.23 |
Rv3236c | 3612381 | c.736C>T | synonymous_variant | 0.29 |
Rv3236c | 3612388 | c.729T>G | synonymous_variant | 0.47 |
Rv3236c | 3612813 | p.Thr102Pro | missense_variant | 0.18 |
Rv3236c | 3613168 | c.-52A>G | upstream_gene_variant | 1.0 |
fbiA | 3640738 | p.Met66Leu | missense_variant | 1.0 |
alr | 3840402 | p.Arg340Leu | missense_variant | 1.0 |
rpoA | 3878248 | p.Ser87Trp | missense_variant | 0.2 |
rpoA | 3878301 | c.207C>A | synonymous_variant | 0.24 |
ddn | 3987090 | p.Glu83Gln | missense_variant | 1.0 |
clpC1 | 4039448 | c.1257A>C | synonymous_variant | 0.18 |
clpC1 | 4039451 | c.1254G>C | synonymous_variant | 0.18 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.25 |
clpC1 | 4039890 | p.Val272Gly | missense_variant | 0.27 |
clpC1 | 4039916 | c.789T>G | synonymous_variant | 0.28 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4239973 | c.111T>G | synonymous_variant | 0.4 |
embC | 4239998 | p.Ala46Pro | missense_variant | 0.25 |
embC | 4240001 | p.Thr47Pro | missense_variant | 0.25 |
embC | 4240006 | c.144A>C | synonymous_variant | 0.42 |
embC | 4240008 | p.Leu49Pro | missense_variant | 0.18 |
embC | 4240017 | p.Val52Gly | missense_variant | 0.18 |
embC | 4240520 | p.Thr220Pro | missense_variant | 0.25 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
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 | 0.25 |
embA | 4243888 | p.Val219Gly | missense_variant | 0.15 |
embA | 4244638 | p.Val469Gly | missense_variant | 0.2 |
embA | 4244641 | p.Val470Gly | missense_variant | 0.3 |
embA | 4244650 | p.Asp473Gly | missense_variant | 0.2 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247629 | c.1116C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248689 | p.Ile726Val | missense_variant | 0.21 |
embB | 4248799 | c.2286T>G | synonymous_variant | 0.2 |
embB | 4249403 | p.Thr964Pro | missense_variant | 0.33 |
aftB | 4268776 | p.Ser21Gly | missense_variant | 0.29 |
aftB | 4268907 | c.-71T>C | upstream_gene_variant | 0.22 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269490 | p.Ala115Gly | missense_variant | 0.25 |
ubiA | 4269502 | p.Val111Gly | missense_variant | 0.22 |
aftB | 4269504 | c.-668A>G | upstream_gene_variant | 0.22 |
ubiA | 4269511 | p.Val108Gly | missense_variant | 0.25 |
ubiA | 4269514 | p.Val107Gly | missense_variant | 0.25 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269848 | c.-15A>G | upstream_gene_variant | 0.22 |
ubiA | 4269864 | c.-31C>G | upstream_gene_variant | 0.43 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 1.0 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
ethA | 4326887 | p.Asp196Gly | missense_variant | 0.31 |
ethR | 4326907 | c.-642C>G | upstream_gene_variant | 0.21 |
ethR | 4327597 | p.Thr17Pro | missense_variant | 0.18 |
ethR | 4327624 | p.Glu26Lys | missense_variant | 0.17 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |