Run ID: ERR9811807
Sample name:
Date: 02-04-2023 13:14:39
Number of reads: 1062620
Percentage reads mapped: 99.74
Strain: lineage4.3.4.2
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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Ala | 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 |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
inhA | 1674782 | p.Ile194Thr | missense_variant | 1.0 | isoniazid, ethionamide |
pncA | 2288868 | p.Val125Gly | missense_variant | 1.0 | pyrazinamide |
embA | 4243217 | c.-16C>T | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
embB | 4247781 | p.Met423Thr | missense_variant | 1.0 | ethambutol |
gid | 4407965 | p.Ala80Pro | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 1.0 |
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 | 490655 | c.-128T>C | upstream_gene_variant | 1.0 |
mshA | 576483 | p.Val379Gly | missense_variant | 0.27 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.33 |
mshA | 576693 | p.Asn449Thr | missense_variant | 0.25 |
rpoB | 761998 | p.Leu731Pro | missense_variant | 1.0 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.29 |
rpoC | 764995 | c.1626C>G | synonymous_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 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.11 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.11 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.11 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918621 | p.Ser228Arg | missense_variant | 0.28 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289787 | c.-546A>C | upstream_gene_variant | 0.2 |
thyX | 3067958 | c.-13T>G | upstream_gene_variant | 0.19 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339044 | c.-74T>G | upstream_gene_variant | 0.26 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.67 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474212 | p.Lys69Thr | missense_variant | 0.19 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
alr | 3841433 | c.-13G>C | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245835 | p.Leu868Arg | missense_variant | 0.33 |
embB | 4247033 | p.Ser174Arg | missense_variant | 0.22 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.12 |
aftB | 4267418 | c.1419G>A | synonymous_variant | 0.1 |
aftB | 4267902 | p.Val312Gly | missense_variant | 0.18 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.33 |
ethR | 4328041 | p.Thr165Pro | missense_variant | 0.19 |
ethA | 4328127 | c.-654C>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |