Run ID: ERR216914
Sample name:
Date: 20-10-2023 22:55:53
Number of reads: 2591700
Percentage reads mapped: 99.5
Strain: lineage4.4.1.2;lineage4.3.4.2.1
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 | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.25 |
lineage4.4 | Euro-American | S;T | None | 0.75 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 0.78 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 0.2 |
lineage4.4.1.2 | Euro-American | T1 | None | 0.72 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 0.24 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 0.26 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 0.32 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.22 |
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 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 0.63 |
PPE35 | 2167770 | p.Ser948Ile | missense_variant | 0.76 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 0.63 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.86 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2860213 | p.Pro69Leu | missense_variant | 0.75 |
ribD | 2986868 | c.30T>C | synonymous_variant | 0.76 |
thyX | 3067754 | c.192C>T | synonymous_variant | 0.59 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.33 |
ald | 3086738 | c.-82C>T | upstream_gene_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 0.73 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 0.37 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249012 | c.2499G>A | synonymous_variant | 0.76 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.36 |