Run ID: SRR1165236
Sample name:
Date: 02-04-2023 23:47:56
Number of reads: 2287012
Percentage reads mapped: 52.16
Strain: lineage2.2
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 0.68 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761110 | p.Asp435Val | missense_variant | 0.97 | rifampicin |
rrs | 1472359 | n.514A>C | non_coding_transcript_exon_variant | 0.92 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.84 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673423 | c.-17G>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288724 | c.517dupG | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
alr | 3841083 | p.Leu113Arg | missense_variant | 1.0 | cycloserine |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
ethA | 4326333 | p.Ala381Pro | missense_variant | 1.0 | ethionamide |
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7581 | p.Asp94Ser | missense_variant | 0.19 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472108 | n.263C>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472129 | n.284G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472135 | n.290C>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472153 | n.308G>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.21 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.97 |
Rv1979c | 2221939 | p.Arg409Gln | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2859623 | p.Pro266Ala | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612286 | c.830dupG | frameshift_variant | 0.2 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |