Run ID: SRR2101359
Sample name:
Date: 19-10-2023 17:19:13
Number of reads: 1019891
Percentage reads mapped: 99.47
Strain: lineage4.4.1.1;lineage3
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 |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.52 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.5 |
lineage4.4 | Euro-American | S;T | None | 0.54 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 0.55 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 0.44 |
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 | 8056 | p.Arg252Leu | missense_variant | 0.66 |
gyrA | 9138 | p.Gln613Glu | missense_variant | 0.6 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.39 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 0.6 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.27 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.42 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.51 |
mmpL5 | 777416 | c.1065G>T | synonymous_variant | 0.61 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 0.71 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.38 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.45 |
PPE35 | 2168479 | p.Thr712Pro | missense_variant | 0.54 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 0.39 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.42 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.57 |
thyA | 3074424 | c.48G>T | synonymous_variant | 0.41 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 0.48 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568779 | c.-100T>C | upstream_gene_variant | 0.53 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 0.27 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.66 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4328212 | c.-740delC | upstream_gene_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.69 |