Run ID: ERR2515482
Sample name:
Date: 31-03-2023 20:57:38
Number of reads: 574674
Percentage reads mapped: 99.76
Strain: lineage4.8
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 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 760314 | p.Val170Phe | missense_variant | 1.0 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 762201 | p.Lys799Gln | missense_variant | 1.0 |
rpoC | 765927 | p.Thr853Ser | missense_variant | 1.0 |
rpoC | 766544 | p.Glu1059Lys | missense_variant | 0.11 |
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 | 1473733 | n.76C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474564 | n.907G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475037 | n.1380T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475481 | n.1824C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476274 | n.2617G>A | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102813 | p.Arg77Pro | missense_variant | 1.0 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.12 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.17 |
PPE35 | 2170532 | c.81G>A | synonymous_variant | 0.12 |
PPE35 | 2170655 | c.-43G>T | upstream_gene_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518766 | p.Thr218Ala | missense_variant | 0.11 |
ribD | 2986778 | c.-61G>A | upstream_gene_variant | 1.0 |
Rv3236c | 3613295 | c.-179G>T | upstream_gene_variant | 0.11 |
fbiB | 3641823 | p.Asn97Asp | missense_variant | 0.13 |
rpoA | 3878402 | p.Asn36Tyr | missense_variant | 0.15 |
embC | 4240147 | c.285C>T | synonymous_variant | 1.0 |
embC | 4241643 | p.Ala594Glu | missense_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244669 | c.1437G>T | synonymous_variant | 0.1 |
embA | 4245422 | c.2190G>A | synonymous_variant | 0.1 |
aftB | 4267149 | p.Glu563Gly | missense_variant | 1.0 |
aftB | 4267155 | p.Gln561Arg | missense_variant | 1.0 |
aftB | 4268503 | p.Gly112Ser | missense_variant | 0.2 |
aftB | 4268544 | p.Leu98Pro | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408239 | c.-37A>G | upstream_gene_variant | 0.12 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |