Run ID: ERR9806866
Sample name:
Date: 18-05-2023 17:17:35
Number of reads: 2443162
Percentage reads mapped: 99.55
Strain: lineage4.1.1.3
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Ser450Leu (1.00) |
Isoniazid | R | katG p.Ile393Asn (0.13), katG p.Ser315Thr (1.00), ahpC c.-48G>A (1.00) |
Ethambutol | R | embB p.Met306Val (1.00) |
Pyrazinamide | R | pncA p.Val139Met (1.00) |
Streptomycin | R | rpsL p.Lys43Arg (1.00) |
Fluoroquinolones | R | gyrA p.Gly88Cys (1.00) |
Moxifloxacin | R | gyrA p.Gly88Cys (1.00) |
Ofloxacin | R | gyrA p.Gly88Cys (1.00) |
Levofloxacin | R | gyrA p.Gly88Cys (1.00) |
Ciprofloxacin | R | gyrA p.Gly88Cys (1.00) |
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | R | ethA c.597delC (1.00), ethA c.597delC (1.00) |
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
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 | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7563 | p.Gly88Cys | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2154934 | p.Ile393Asn | missense_variant | 0.13 | isoniazid |
katG | 2155167 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288827 | p.Val139Met | missense_variant | 1.0 | pyrazinamide |
ahpC | 2726145 | c.-48G>A | upstream_gene_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326876 | c.597delC | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5701 | c.466delC | frameshift_variant | 0.11 |
gyrB | 6608 | p.Val457Leu | missense_variant | 1.0 |
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 | 490780 | c.-3C>A | upstream_gene_variant | 0.17 |
mshA | 576469 | c.1122G>T | synonymous_variant | 0.12 |
mshA | 576590 | p.Arg415Trp | missense_variant | 0.17 |
ccsA | 619710 | c.-181G>T | upstream_gene_variant | 0.15 |
rpoC | 764744 | c.1375C>A | synonymous_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765842 | p.Thr825Ala | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777701 | c.780C>T | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801354 | c.546G>A | synonymous_variant | 1.0 |
fbiC | 1304253 | c.1323G>T | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154463 | p.Ala550Val | missense_variant | 0.12 |
PPE35 | 2169900 | p.Gly238Val | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3065301 | c.891C>A | synonymous_variant | 0.18 |
Rv2752c | 3065364 | c.828G>T | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3338995 | c.-123G>A | upstream_gene_variant | 0.14 |
fbiD | 3339103 | c.-15T>C | upstream_gene_variant | 0.18 |
Rv3083 | 3449616 | p.Met371Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474652 | c.648delC | frameshift_variant | 0.11 |
clpC1 | 4039405 | p.Glu434* | stop_gained | 0.15 |
clpC1 | 4040307 | c.397delC | frameshift_variant | 0.11 |
embC | 4242072 | p.Gly737Asp | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243494 | p.Leu88Met | missense_variant | 0.12 |
embB | 4247161 | c.648G>A | synonymous_variant | 0.12 |
embB | 4248705 | p.Pro731Gln | missense_variant | 0.12 |
embB | 4248717 | p.Asn735Ser | missense_variant | 0.12 |
embB | 4249041 | p.Pro843Arg | missense_variant | 0.11 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
aftB | 4267750 | p.Phe363Leu | missense_variant | 0.11 |
aftB | 4267878 | p.Val320Gly | missense_variant | 0.33 |
aftB | 4267938 | p.Arg300Gln | missense_variant | 0.14 |
ubiA | 4269760 | p.Gln25Leu | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |