Run ID: ERR4972590
Sample name:
Date: 01-04-2023 21:48:07
Number of reads: 127925
Percentage reads mapped: 6.1
Strain: lineage4
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289213 | p.Gln10Pro | missense_variant | 1.0 | pyrazinamide |
embB | 4247730 | p.Gly406Ala | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7611 | p.Ser104Pro | missense_variant | 0.4 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
rpoB | 760007 | c.201C>T | synonymous_variant | 0.25 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761632 | p.Ala609Glu | missense_variant | 0.33 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777793 | p.Ala230Thr | missense_variant | 1.0 |
mmpL5 | 777812 | p.Tyr223* | stop_gained | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303458 | c.528G>A | synonymous_variant | 0.29 |
fbiC | 1303802 | p.Ile291Asn | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474573 | n.916C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474584 | n.927C>G | non_coding_transcript_exon_variant | 0.4 |
ndh | 2102185 | c.857dupG | frameshift_variant | 1.0 |
katG | 2154224 | p.Gly630Cys | missense_variant | 0.29 |
PPE35 | 2169751 | p.Gly288* | stop_gained | 1.0 |
Rv1979c | 2222777 | p.Ala130Thr | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517984 | c.-131G>T | upstream_gene_variant | 0.2 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
pepQ | 2859525 | c.894T>A | synonymous_variant | 0.4 |
pepQ | 2860184 | c.229_234delCGCGCG | conservative_inframe_deletion | 0.2 |
pepQ | 2860200 | c.219G>A | synonymous_variant | 0.22 |
pepQ | 2860201 | c.216_217delAG | frameshift_variant | 0.29 |
pepQ | 2860207 | c.211_212insGCGCGC | conservative_inframe_insertion | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087721 | p.Met301Thr | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475061 | p.Pro352His | missense_variant | 0.5 |
clpC1 | 4040590 | p.His39Asp | missense_variant | 0.4 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245386 | c.2154C>T | synonymous_variant | 0.15 |
embB | 4247024 | p.Pro171Ala | missense_variant | 0.67 |
embB | 4247915 | p.Arg468Ser | missense_variant | 0.22 |
embB | 4249209 | p.Val899Ala | missense_variant | 0.18 |
ethA | 4326119 | p.Arg452Pro | missense_variant | 1.0 |
whiB6 | 4338579 | c.-58C>A | upstream_gene_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |