Run ID: SRR22175241
Sample name:
Date: 04-04-2023 04:02:30
Number of reads: 1226635
Percentage reads mapped: 99.48
Strain: lineage4.3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.95 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.91 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 0.92 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288718 | c.523delA | frameshift_variant | 1.0 | pyrazinamide |
embA | 4243217 | c.-16C>T | upstream_gene_variant | 0.92 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7581 | p.Asp94Arg | missense_variant | 0.88 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 759836 | c.30C>G | synonymous_variant | 0.1 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.87 |
rpoC | 765570 | p.Ala734Val | missense_variant | 0.91 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776203 | p.Gly760Cys | missense_variant | 0.12 |
mmpS5 | 779561 | c.-656C>T | upstream_gene_variant | 0.12 |
mmpS5 | 779670 | c.-765A>G | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473022 | n.1177G>T | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.88 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.92 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4326296 | p.Leu393Arg | missense_variant | 0.13 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 0.11 |
ethA | 4327269 | p.Trp69Arg | missense_variant | 0.92 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408063 | p.Arg47Leu | missense_variant | 0.97 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.97 |
whiB6 | 4338199 | c.-10_322del | frameshift_variant&start_lost | 1.0 |