Run ID: SRR7341648
Sample name:
Date: 19-10-2023 19:08:28
Number of reads: 4057738
Percentage reads mapped: 99.55
Strain: lineage4.1.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Gln432Pro (1.00) |
Isoniazid | R | katG c.1548_1549dupGG (0.99), katG c.2_6dupTGCCC (1.00), ahpC c.-52C>T (1.00) |
Ethambutol | R | embA c.-12C>T (1.00) |
Pyrazinamide | R | pncA p.Gln10Arg (1.00) |
Streptomycin | ||
Fluoroquinolones | R | gyrA p.Ser91Pro (1.00) |
Moxifloxacin | R | gyrA p.Ser91Pro (1.00) |
Ofloxacin | R | gyrA p.Ser91Pro (1.00) |
Levofloxacin | R | gyrA p.Ser91Pro (1.00) |
Ciprofloxacin | R | gyrA p.Ser91Pro (1.00) |
Aminoglycosides | R | rrs n.1401A>G (1.00) |
Amikacin | R | rrs n.1401A>G (1.00) |
Capreomycin | R | rrs n.1401A>G (1.00) |
Kanamycin | R | rrs n.1401A>G (1.00) |
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7572 | p.Ser91Pro | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761101 | p.Gln432Pro | missense_variant | 1.0 | rifampicin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2154562 | c.1548_1549dupGG | frameshift_variant | 0.99 | isoniazid |
katG | 2156105 | c.2_6dupTGCCC | frameshift_variant | 1.0 | isoniazid |
pncA | 2289213 | p.Gln10Arg | missense_variant | 1.0 | pyrazinamide |
ahpC | 2726141 | c.-52C>T | upstream_gene_variant | 1.0 | isoniazid |
embA | 4243221 | c.-12C>T | upstream_gene_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.99 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575332 | c.-16T>G | upstream_gene_variant | 0.99 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.19 |
mshA | 576221 | p.Gly292Arg | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 762112 | p.Asn769Thr | missense_variant | 1.0 |
rpoB | 762714 | p.Val970Met | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766759 | c.3390G>A | synonymous_variant | 1.0 |
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 | 1474578 | n.921A>G | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154647 | p.Arg489Cys | missense_variant | 1.0 |
katG | 2156309 | c.-198G>C | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087307 | c.489delG | frameshift_variant | 0.73 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
ubiA | 4269671 | p.Val55Leu | missense_variant | 1.0 |
ethA | 4326908 | p.Thr189Lys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |