Run ID: ERR4817795
Sample name:
Date: 20-10-2023 08:29:27
Number of reads: 3035405
Percentage reads mapped: 93.14
Strain: lineage4.7
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | R | rrs n.888G>A (0.81) |
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 |
lineage4.7 | Euro-American (mainly T) | T1;T5 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.81 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6415 | c.-887G>A | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_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 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.36 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
alr | 3840618 | p.Asp268Gly | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249732 | c.3219C>G | synonymous_variant | 1.0 |
ubiA | 4269933 | c.-100C>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |