Run ID: SRR9971229
Sample name:
Date: 04-04-2023 23:18:07
Number of reads: 8789487
Percentage reads mapped: 98.76
Strain: lineage4.3.2.1
Drug-resistance: RR-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 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 1.0 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761108 | p.Met434Ile | missense_variant | 1.0 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrA | 7222 | c.-80C>T | upstream_gene_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 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.28 |
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 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475760 | n.2103C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.98 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.21 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407582 | c.621T>C | synonymous_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |