Run ID: ERR11465833
Sample name:
Date: 10-01-2024 04:33:23
Number of reads: 3540957
Percentage reads mapped: 99.51
Strain: lineage4.3.2.1
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 | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 0.98 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.99 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.18 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.14 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.13 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.11 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.14 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.14 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.15 |
rpoC | 764326 | c.957G>C | synonymous_variant | 0.14 |
rpoC | 764338 | p.Glu323Asp | missense_variant | 0.2 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.13 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.11 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.11 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.12 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.97 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474558 | n.901G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.11 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.15 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290107 | c.-866T>A | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.99 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338460 | p.Met21Arg | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |