Run ID: SRR5818667
Sample name:
Date: 21-10-2023 05:06:15
Number of reads: 2504052
Percentage reads mapped: 92.85
Strain: lineage4.4.1.1
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 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 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 762053 | c.2247T>C | 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 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223174 | c.-10C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |