Run ID: SRR23861777
Sample name:
Date: 12-04-2023 03:34:18
Number of reads: 2849047
Percentage reads mapped: 99.65
Strain: lineage4.8
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 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 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 |
mshA | 576093 | p.Pro249Arg | missense_variant | 0.24 |
mshA | 576100 | p.Asp251Glu | missense_variant | 0.13 |
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 | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3066031 | p.Glu54Ala | missense_variant | 1.0 |
ald | 3087095 | c.276C>T | synonymous_variant | 1.0 |
whiB7 | 3568401 | c.279G>T | stop_lost&splice_region_variant | 0.15 |
whiB7 | 3568416 | p.Lys88His | missense_variant | 0.19 |
whiB7 | 3568428 | c.252A>C | synonymous_variant | 0.34 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.18 |
clpC1 | 4038186 | p.Ala840Gly | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246552 | p.Asn13Lys | missense_variant | 0.26 |
embB | 4246559 | p.Ile16Leu | missense_variant | 0.12 |
embB | 4246569 | p.Ala19Gly | missense_variant | 0.21 |
embB | 4246574 | p.Ala21Ser | missense_variant | 0.2 |
embB | 4247013 | p.Pro167Arg | missense_variant | 0.18 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.14 |
embB | 4247023 | c.510G>C | synonymous_variant | 0.14 |
embB | 4247027 | p.Leu172Gly | missense_variant | 0.14 |
ethA | 4328004 | c.-531C>A | upstream_gene_variant | 0.2 |
ethA | 4328025 | c.-552T>A | upstream_gene_variant | 0.18 |
ethR | 4328030 | p.Ala161Gly | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |