Run ID: ERR4812878
Sample name:
Date: 01-04-2023 12:23:50
Number of reads: 5713790
Percentage reads mapped: 99.57
Strain: lineage4
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
fabG1 | 1673423 | c.-17G>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
embB | 4247431 | p.Met306Ile | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576222 | p.Gly292Val | missense_variant | 0.5 |
mshA | 576292 | c.945C>T | synonymous_variant | 0.12 |
rpoB | 761889 | p.Val695Leu | missense_variant | 1.0 |
rpoC | 764817 | p.Val483Gly | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801009 | c.201A>G | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155751 | p.Gly121Ser | missense_variant | 1.0 |
PPE35 | 2170317 | p.Ala99Asp | missense_variant | 0.12 |
Rv1979c | 2223214 | c.-50A>C | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518721 | p.Glu203* | stop_gained | 0.14 |
eis | 2714951 | p.Arg128Trp | missense_variant | 0.33 |
folC | 2747783 | c.-185G>A | upstream_gene_variant | 0.13 |
pepQ | 2859990 | c.429G>A | synonymous_variant | 0.22 |
pepQ | 2860044 | c.375C>A | synonymous_variant | 0.17 |
pepQ | 2860079 | p.Leu114Met | missense_variant | 0.17 |
pepQ | 2860095 | c.324C>T | synonymous_variant | 0.17 |
Rv2752c | 3065517 | c.675C>T | synonymous_variant | 1.0 |
thyX | 3067564 | c.382C>T | synonymous_variant | 0.14 |
Rv3083 | 3448439 | c.-64delA | upstream_gene_variant | 1.0 |
fprA | 3474299 | p.Asp98Gly | missense_variant | 1.0 |
Rv3236c | 3612132 | p.Ala329Ser | missense_variant | 0.15 |
rpoA | 3878595 | c.-88C>T | upstream_gene_variant | 0.39 |
clpC1 | 4038167 | c.2538C>T | synonymous_variant | 0.18 |
embC | 4240525 | c.663C>A | synonymous_variant | 0.5 |
embC | 4241159 | p.Ala433Thr | missense_variant | 0.22 |
embC | 4242320 | p.Pro820Ser | missense_variant | 0.17 |
embA | 4242343 | c.-890G>T | upstream_gene_variant | 0.25 |
embC | 4242363 | p.Gly834Val | missense_variant | 0.4 |
embA | 4243681 | p.Ala150Asp | missense_variant | 0.11 |
embB | 4246918 | c.405G>T | synonymous_variant | 0.19 |
embB | 4246999 | c.486C>T | synonymous_variant | 0.12 |
embB | 4247738 | p.Ala409Thr | missense_variant | 0.13 |
ethA | 4328317 | c.-844C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |