Run ID: ERR176464
Sample name:
Date: 24-01-2024 12:25:04
Number of reads: 4140939
Percentage reads mapped: 84.35
Strain: lineage3.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | R | rrs n.888G>A (0.46) |
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
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 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.46 | streptomycin |
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 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.99 |
rpoC | 762434 | c.-936T>G | upstream_gene_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 | 0.99 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.12 |
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 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
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 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embC | 4241562 | p.Arg567His | missense_variant | 0.99 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |