Run ID: ERR11081762
Sample name:
Date: 09-04-2023 09:09:37
Number of reads: 735474
Percentage reads mapped: 99.43
Strain: lineage4.2.1
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 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ahpC | 2726145 | c.-48G>A | upstream_gene_variant | 1.0 | isoniazid |
embB | 4247730 | p.Gly406Ala | missense_variant | 1.0 | ethambutol |
pncA | 2282095 | c.-1470_*6585del | transcript_ablation | 1.0 | pyrazinamide |
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 |
fgd1 | 491247 | c.465C>T | synonymous_variant | 1.0 |
mshA | 575855 | p.Ala170Thr | missense_variant | 0.25 |
ccsA | 619969 | p.Val27Ile | missense_variant | 1.0 |
rpoC | 764363 | p.Gly332Ser | missense_variant | 1.0 |
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 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.16 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519041 | c.927C>T | synonymous_variant | 0.18 |
pepQ | 2860618 | c.-200C>T | upstream_gene_variant | 0.12 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.15 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.15 |
embC | 4241750 | c.1888T>C | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242795 | p.Ala978Val | missense_variant | 0.12 |
embA | 4243785 | c.553C>T | synonymous_variant | 0.14 |
embA | 4245643 | c.2413_2414dupGC | frameshift_variant | 0.22 |
embB | 4246145 | c.-369C>T | upstream_gene_variant | 0.2 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.14 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.14 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.15 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.15 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.15 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.15 |
embB | 4249543 | c.3030G>A | synonymous_variant | 0.22 |
embB | 4249594 | c.3081G>A | synonymous_variant | 1.0 |
aftB | 4267976 | c.861G>A | synonymous_variant | 0.12 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |