Run ID: ERR4820845
Sample name:
Date: 01-04-2023 16:54:43
Number of reads: 1262480
Percentage reads mapped: 89.21
Strain: lineage4.8
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 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288808 | c.433delG | frameshift_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9432 | p.Leu711Met | missense_variant | 1.0 |
ccsA | 620358 | c.468C>T | synonymous_variant | 1.0 |
rpoB | 761593 | p.Ala596Gly | missense_variant | 1.0 |
rpoC | 763058 | c.-312C>T | upstream_gene_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776995 | p.Ser496Pro | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406631 | p.Ala237Val | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472553 | n.708C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472572 | n.727T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472574 | n.729T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472584 | n.739A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472594 | n.749G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472714 | n.869A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473733 | n.76C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168105 | c.2508C>T | synonymous_variant | 0.11 |
PPE35 | 2168466 | p.Leu716His | missense_variant | 0.1 |
Rv1979c | 2223006 | c.158delT | frameshift_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289917 | c.-676G>T | upstream_gene_variant | 0.1 |
Rv2752c | 3066055 | p.Gly46Val | missense_variant | 0.11 |
ald | 3086966 | p.Asp49Glu | missense_variant | 1.0 |
clpC1 | 4038749 | c.1955delG | frameshift_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethR | 4327636 | c.89delT | frameshift_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |