Run ID: ERR11465954
Sample name:
Date: 10-01-2024 06:08:56
Number of reads: 2566356
Percentage reads mapped: 99.74
Strain: lineage4.9;lineage4.8.1
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 |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.85 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.05 |
lineage4.8.1 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.69 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.91 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.23 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.95 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476704 | n.3053delC | non_coding_transcript_exon_variant | 0.81 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.91 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 0.81 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.95 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.16 |
fbiD | 3339040 | c.-78T>C | upstream_gene_variant | 0.62 |
fbiD | 3339113 | c.-5A>C | upstream_gene_variant | 0.61 |
fbiB | 3642874 | p.Leu447Arg | missense_variant | 0.91 |
alr | 3840950 | p.Lys157Asn | missense_variant | 0.16 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.79 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.42 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.26 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.32 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.32 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.31 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.32 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.96 |