Run ID: SRR1196587
Sample name:
Date: 03-04-2023 05:29:32
Number of reads: 1167513
Percentage reads mapped: 96.45
Strain: lineage4.3.3
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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rrs | 1472753 | n.908A>G | non_coding_transcript_exon_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ahpC | 2726141 | c.-52C>T | upstream_gene_variant | 1.0 | isoniazid |
embA | 4243217 | c.-16C>T | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247730 | p.Gly406Ala | missense_variant | 1.0 | ethambutol |
ethA | 4327484 | c.-11A>G | upstream_gene_variant | 0.96 | ethionamide |
pncA | 2288565 | c.377_*115del | frameshift_variant&stop_lost&splice_region_variant | 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 | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 761547 | p.Val581Met | missense_variant | 0.97 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.13 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.12 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.17 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.18 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.16 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.16 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.15 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.13 |
rpoC | 762419 | c.-951C>G | upstream_gene_variant | 0.12 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.1 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.15 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.1 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.1 |
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 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223051 | p.Glu38Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyX | 3067313 | c.633G>T | synonymous_variant | 0.11 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.12 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.13 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.13 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.14 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.11 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.11 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.11 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.1 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.13 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.23 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.21 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.15 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.15 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.13 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.12 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.13 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.13 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.12 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.17 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.14 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.14 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.17 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4242115 | c.2253G>A | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4407912 | c.160_290del | frameshift_variant | 1.0 |