Run ID: ERR1199093
Sample name:
Date: 31-03-2023 12:34:40
Number of reads: 593692
Percentage reads mapped: 99.67
Strain: lineage4.6.1.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 0.99 |
lineage4.6.1 | Euro-American (Uganda) | T2 | RD724 | 1.0 |
lineage4.6.1.2 | Euro-American | T2 | RD724 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761100 | p.Gln432Glu | missense_variant | 1.0 | rifampicin |
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289202 | p.Cys14Gly | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5092 | c.-148A>T | upstream_gene_variant | 0.21 |
gyrB | 6142 | c.903G>T | synonymous_variant | 0.3 |
gyrB | 6705 | p.Glu489Val | missense_variant | 0.4 |
gyrB | 6749 | p.Ala504Ser | missense_variant | 0.5 |
gyrB | 7072 | p.Lys611Asn | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7539 | p.Thr80Ala | missense_variant | 1.0 |
gyrA | 7570 | p.Ala90Gly | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7897 | p.Asp199Ala | missense_variant | 0.25 |
gyrA | 9280 | p.Val660Gly | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 763428 | p.Ile20Asn | missense_variant | 0.15 |
rpoC | 764810 | p.Pro481Thr | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776226 | p.Glu752Val | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303219 | p.Leu97Ile | missense_variant | 0.17 |
fbiC | 1303519 | p.Ser197Arg | missense_variant | 0.25 |
embR | 1416410 | p.Leu313Arg | missense_variant | 1.0 |
atpE | 1460965 | c.-80A>T | upstream_gene_variant | 0.3 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473307 | n.1462A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475373 | n.1716G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475472 | n.1815T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475822 | n.2165A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475886 | n.2229T>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476371 | n.2714A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476441 | n.2784T>G | non_coding_transcript_exon_variant | 0.25 |
inhA | 1674799 | p.Ser200Cys | missense_variant | 0.17 |
tlyA | 1917826 | c.-114A>C | upstream_gene_variant | 0.3 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102356 | c.687T>G | synonymous_variant | 0.18 |
katG | 2154323 | p.Tyr597Asn | missense_variant | 0.23 |
katG | 2154705 | c.1407C>G | synonymous_variant | 0.15 |
katG | 2156403 | c.-292A>C | upstream_gene_variant | 0.14 |
PPE35 | 2168447 | p.Gln722His | missense_variant | 0.33 |
PPE35 | 2168631 | p.Asn661Ser | missense_variant | 1.0 |
PPE35 | 2168681 | p.Phe644Leu | missense_variant | 0.4 |
PPE35 | 2169725 | p.Asn296Lys | missense_variant | 0.38 |
PPE35 | 2169880 | p.Phe245Ile | missense_variant | 0.22 |
PPE35 | 2169917 | c.696T>A | synonymous_variant | 0.38 |
Rv1979c | 2222596 | p.Val190Gly | missense_variant | 0.22 |
Rv1979c | 2223064 | p.Leu34Gln | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290020 | c.-779T>A | upstream_gene_variant | 0.29 |
eis | 2714878 | p.Asp152Ala | missense_variant | 0.18 |
pepQ | 2859563 | p.Tyr286Asp | missense_variant | 0.17 |
pepQ | 2860249 | p.Asp57Ala | missense_variant | 0.22 |
pepQ | 2860324 | p.Tyr32Phe | missense_variant | 0.14 |
pepQ | 2860592 | c.-174T>A | upstream_gene_variant | 0.67 |
Rv2752c | 3065836 | p.Tyr119Phe | missense_variant | 0.25 |
Rv2752c | 3065920 | p.Pro91Leu | missense_variant | 1.0 |
Rv2752c | 3065995 | p.His66Leu | missense_variant | 0.17 |
thyA | 3074318 | p.Phe52Ile | missense_variant | 0.29 |
ald | 3086749 | c.-71T>A | upstream_gene_variant | 0.55 |
Rv3083 | 3448741 | p.Ser80Ala | missense_variant | 0.43 |
Rv3083 | 3449227 | p.Phe242Leu | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612327 | p.Thr264Ala | missense_variant | 0.25 |
fbiA | 3640449 | c.-94T>A | upstream_gene_variant | 0.25 |
fbiA | 3640502 | c.-41C>A | upstream_gene_variant | 0.29 |
alr | 3840529 | p.Thr298Ser | missense_variant | 0.44 |
rpoA | 3878031 | c.477T>A | synonymous_variant | 0.4 |
rpoA | 3878300 | p.Lys70* | stop_gained | 0.25 |
ddn | 3987215 | c.372A>G | synonymous_variant | 1.0 |
clpC1 | 4038634 | p.Glu691Lys | missense_variant | 0.17 |
clpC1 | 4040409 | p.Gly99Val | missense_variant | 0.43 |
clpC1 | 4040604 | p.Leu34His | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.95 |
embA | 4244396 | c.1164T>G | synonymous_variant | 0.14 |
embA | 4244508 | p.Leu426Val | missense_variant | 0.27 |
embA | 4244905 | p.Val558Gly | missense_variant | 0.25 |
embA | 4245020 | c.1788T>G | synonymous_variant | 0.2 |
embA | 4245055 | p.Thr608Asn | missense_variant | 1.0 |
embB | 4248665 | p.Phe718Val | missense_variant | 0.14 |
embB | 4249016 | p.Tyr835Asn | missense_variant | 0.33 |
embB | 4249785 | p.Pro1091Gln | missense_variant | 0.33 |
aftB | 4267365 | p.Met491Lys | missense_variant | 0.22 |
aftB | 4268874 | c.-38T>G | upstream_gene_variant | 0.23 |
aftB | 4269471 | c.-635C>A | upstream_gene_variant | 0.27 |
ethA | 4326171 | p.Thr435Ala | missense_variant | 0.33 |
ethA | 4327451 | p.Val8Gly | missense_variant | 0.5 |
ethR | 4328092 | p.Thr182Pro | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408093 | p.Gly37Val | missense_variant | 1.0 |
gid | 4408444 | c.-242A>C | upstream_gene_variant | 0.57 |