Run ID: ERR4817840
Sample name:
Date: 20-10-2023 08:30:29
Number of reads: 3669606
Percentage reads mapped: 97.22
Strain: lineage3.1.2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | ||
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | R | rrs n.1402C>A (0.28) |
Amikacin | R | rrs n.1402C>A (0.28) |
Capreomycin | R | rrs n.1402C>A (0.28) |
Kanamycin | R | rrs n.1402C>A (0.28) |
Cycloserine | ||
Ethionamide | ||
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.2 | East-African-Indian | CAS;CAS2 | RD750 | 1.0 |
lineage3.1.2.2 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.28 | kanamycin, capreomycin, aminoglycosides, amikacin |
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 |
gyrA | 9611 | c.2310C>T | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | 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 | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473022 | n.1177G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473292 | n.1447_1449delGGAinsTGGG | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474662 | n.1005C>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475526 | n.1869C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.27 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.12 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.13 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.99 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168604 | p.Pro670Leu | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087476 | c.657C>T | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.99 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4326176 | p.Glu433Ala | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |