Run ID: ERR11068551
Sample name:
Date: 13-04-2023 18:08:07
Number of reads: 3638506
Percentage reads mapped: 99.39
Strain: lineage4.3
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 | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 |
mshA | 576116 | p.Ala257Pro | missense_variant | 0.5 |
mshA | 576119 | p.Ala258Pro | missense_variant | 0.75 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779322 | p.Met111Ile | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471786 | n.-60T>G | upstream_gene_variant | 0.23 |
rpsA | 1834299 | p.Gln253Arg | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918066 | p.Ala43Pro | missense_variant | 0.2 |
tlyA | 1918302 | c.363G>C | synonymous_variant | 0.12 |
tlyA | 1918501 | p.Gly188Arg | missense_variant | 1.0 |
ndh | 2102367 | p.Ala226Thr | missense_variant | 0.11 |
PPE35 | 2168848 | p.Val589Leu | missense_variant | 0.99 |
PPE35 | 2170464 | p.Ala50Val | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715068 | p.Pro89Ser | missense_variant | 0.18 |
folC | 2746601 | p.Val333Asp | missense_variant | 0.17 |
pepQ | 2859968 | p.Asp151Asn | missense_variant | 0.12 |
thyX | 3068055 | c.-110A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339673 | p.Arg186Cys | missense_variant | 0.33 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474914 | p.Ala303Val | missense_variant | 0.12 |
Rv3236c | 3612589 | c.528C>T | synonymous_variant | 0.11 |
fbiB | 3641223 | c.-312C>G | upstream_gene_variant | 0.12 |
fbiA | 3641279 | p.Ile246Thr | missense_variant | 0.17 |
fbiB | 3641301 | c.-234C>G | upstream_gene_variant | 0.12 |
fbiB | 3642218 | c.684A>G | synonymous_variant | 0.17 |
fbiB | 3642225 | p.Gln231* | stop_gained | 0.17 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.23 |
clpC1 | 4038163 | p.Arg848Trp | missense_variant | 0.13 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040257 | p.Ala150Thr | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244261 | c.1029G>A | synonymous_variant | 0.11 |
embA | 4245691 | p.Gly820Ala | missense_variant | 0.17 |
embB | 4246661 | p.Val50Met | missense_variant | 0.11 |
aftB | 4268301 | p.Ala179Asp | missense_variant | 0.11 |
aftB | 4268457 | p.Ala127Val | missense_variant | 1.0 |
aftB | 4269753 | c.-917G>A | upstream_gene_variant | 0.11 |
ethA | 4328453 | c.-980T>C | upstream_gene_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408267 | c.-65T>G | upstream_gene_variant | 1.0 |