Run ID: ERR10748463
Sample name:
Date: 31-03-2023 10:55:36
Number of reads: 3447193
Percentage reads mapped: 99.67
Strain: lineage4.7;lineage4.1.1.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.2 |
lineage4.7 | Euro-American (mainly T) | T1;T5 | None | 0.82 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 0.2 |
lineage4.1.1.1 | Euro-American (X-type) | X2 | RD183 | 0.2 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 0.79 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.83 | rifampicin |
inhA | 1674048 | c.-154G>A | upstream_gene_variant | 0.79 | isoniazid, ethionamide |
katG | 2155167 | p.Ser315Thr | missense_variant | 0.78 | isoniazid |
pncA | 2288952 | p.Gly97Asp | missense_variant | 0.76 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 0.75 | ethambutol |
ethA | 4326449 | p.Thr342Lys | missense_variant | 0.89 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.27 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.25 |
rpoC | 764817 | p.Val483Gly | missense_variant | 0.83 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474294 | n.637C>G | non_coding_transcript_exon_variant | 0.63 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.16 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.64 |
fbiD | 3339746 | p.Ala210Gly | missense_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.19 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 0.15 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 0.2 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.27 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.15 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.25 |
embB | 4249408 | c.2895G>A | synonymous_variant | 0.23 |
embB | 4249732 | c.3219C>G | synonymous_variant | 0.9 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407704 | p.Ala167Pro | missense_variant | 0.8 |