Run ID: ERR2653048
Sample name:
Date: 31-03-2023 22:27:58
Number of reads: 655930
Percentage reads mapped: 99.13
Strain: lineage4.1.2.1
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 |
lineage4.1 | Euro-American | T;X;H | None | 0.98 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.88 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761109 | p.Asp435Tyr | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.27 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288826 | p.Val139Gly | missense_variant | 1.0 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
embB | 4248002 | p.Gln497Lys | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5225 | c.-15G>C | upstream_gene_variant | 0.12 |
gyrB | 6438 | p.Pro400Arg | missense_variant | 1.0 |
gyrA | 7219 | c.-83C>T | upstream_gene_variant | 0.12 |
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 | 491071 | p.Tyr97His | missense_variant | 0.1 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.94 |
mshA | 575196 | c.-152A>T | upstream_gene_variant | 0.12 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.15 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 760629 | c.823C>T | synonymous_variant | 0.12 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.13 |
rpoB | 761277 | p.Ile491Leu | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765376 | c.2007C>A | synonymous_variant | 0.12 |
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 | 1471891 | n.46C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472950 | n.1105C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475388 | n.1731A>T | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674948 | p.Trp249* | stop_gained | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155219 | p.Leu298Ser | missense_variant | 0.12 |
PPE35 | 2168001 | p.Leu871Gln | missense_variant | 0.17 |
PPE35 | 2169017 | p.Leu532Phe | missense_variant | 0.29 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 0.29 |
Rv1979c | 2222149 | p.Arg339Leu | missense_variant | 0.12 |
Rv1979c | 2222665 | p.Thr167Met | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289479 | c.-238G>A | upstream_gene_variant | 0.12 |
pncA | 2289548 | c.-307C>T | upstream_gene_variant | 0.11 |
pncA | 2289871 | c.-630T>C | upstream_gene_variant | 0.12 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518955 | p.Ala281Thr | missense_variant | 0.13 |
folC | 2746822 | p.Glu259Asp | missense_variant | 0.12 |
pepQ | 2860584 | c.-166C>G | upstream_gene_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086896 | c.79dupA | frameshift_variant | 0.2 |
ald | 3087613 | c.796delG | frameshift_variant | 0.46 |
Rv3083 | 3448689 | c.186C>T | synonymous_variant | 0.11 |
Rv3083 | 3448965 | c.464delG | frameshift_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474731 | p.Gly242Val | missense_variant | 0.13 |
whiB7 | 3568710 | c.-31C>A | upstream_gene_variant | 0.15 |
fbiB | 3640728 | c.-807G>C | upstream_gene_variant | 0.18 |
fbiA | 3640766 | p.Pro75Leu | missense_variant | 0.14 |
fbiB | 3642407 | c.873C>T | synonymous_variant | 0.11 |
alr | 3840472 | p.Gly317Ser | missense_variant | 0.12 |
alr | 3841061 | c.360C>T | synonymous_variant | 0.11 |
rpoA | 3878639 | c.-132C>G | upstream_gene_variant | 0.11 |
clpC1 | 4038744 | p.Thr654Met | missense_variant | 0.12 |
embC | 4239935 | p.Asn25Tyr | missense_variant | 0.15 |
embC | 4240074 | p.Glu71Gly | missense_variant | 0.14 |
embC | 4241562 | p.Arg567His | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embC | 4243122 | p.Ser1087Ile | missense_variant | 0.18 |
aftB | 4269792 | c.-956C>A | upstream_gene_variant | 0.12 |
ethA | 4326099 | p.Gln459* | stop_gained | 1.0 |
ethA | 4326441 | p.Asn345Tyr | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |