Run ID: ERR2041700
Sample name:
Date: 18-08-2022 09:23:30
Number of reads: 559925
Percentage reads mapped: 98.83
Strain: lineage4.2.2.1
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 | 0.99 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
lineage4.2.2.1 | Euro-American | LAM7-TUR | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Trp | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289171 | p.Gly24Asp | missense_variant | 1.0 | pyrazinamide |
embB | 4248003 | p.Gln497Arg | 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 | 7615 | p.Leu105Arg | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9525 | p.Val742Leu | missense_variant | 1.0 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
rpoB | 759628 | c.-179C>T | upstream_gene_variant | 0.11 |
rpoB | 759711 | c.-95_-88delGCCGAAAC | upstream_gene_variant | 0.12 |
rpoB | 759726 | c.-81A>T | upstream_gene_variant | 0.11 |
rpoB | 759727 | c.-80A>T | upstream_gene_variant | 0.11 |
rpoB | 759730 | c.-77A>G | upstream_gene_variant | 0.11 |
rpoB | 759733 | c.-74_-73insGTTTCGGC | upstream_gene_variant | 0.12 |
rpoB | 760993 | p.Glu396Val | missense_variant | 0.14 |
rpoB | 762754 | p.Leu983Ser | missense_variant | 0.13 |
rpoC | 766891 | c.3527delT | frameshift_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801297 | c.489C>G | synonymous_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475241 | n.1584C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475607 | n.1950A>G | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673221 | c.-219C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155596 | c.516G>C | synonymous_variant | 0.11 |
kasA | 2518638 | p.Ser175* | stop_gained | 0.17 |
folC | 2746138 | c.1461A>G | synonymous_variant | 0.14 |
thyA | 3074602 | c.-131G>A | upstream_gene_variant | 0.11 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339158 | p.Ile14Thr | missense_variant | 0.12 |
fbiD | 3339215 | p.Gln33Leu | missense_variant | 0.13 |
embC | 4242623 | p.Gly921Cys | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242702 | p.Ala947Val | missense_variant | 0.14 |
embA | 4244958 | p.Ala576Thr | missense_variant | 1.0 |
embB | 4246658 | p.Val49Ile | missense_variant | 0.12 |
embB | 4249535 | c.3025delA | frameshift_variant | 0.15 |
embB | 4249605 | p.Gly1031Asp | missense_variant | 0.15 |