Run ID: ERR5863931
Sample name:
Date: 01-04-2023 23:00:12
Number of reads: 1769603
Percentage reads mapped: 98.19
Strain: lineage2.2.1
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 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrB | 6750 | p.Ala504Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rrs | 1472362 | n.517C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.24 | streptomycin |
inhA | 1674048 | c.-154G>A | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289222 | p.Val7Ala | missense_variant | 1.0 | pyrazinamide |
eis | 2715346 | c.-14C>T | upstream_gene_variant | 1.0 | kanamycin, amikacin |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326705 | c.768delG | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
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 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764817 | p.Val483Gly | missense_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 778922 | c.-442G>T | upstream_gene_variant | 0.12 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475726 | n.2069G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476234 | n.2577G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.24 |
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 | 1.0 |
PPE35 | 2168785 | p.Ile610Val | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339504 | p.Ile129Met | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3841392 | p.Lys10Met | 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 | 4338563 | c.-42G>T | upstream_gene_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 |