Run ID: ERR4812495
Sample name:
Date: 20-10-2023 05:19:21
Number of reads: 3859929
Percentage reads mapped: 94.75
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | R | rrs n.799C>T (0.19) |
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 |
lineage4.1 | 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 |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.19 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417043 | p.Arg102Pro | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
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 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |