Run ID: ERR972802
Sample name:
Date: 02-04-2023 12:02:39
Number of reads: 7276525
Percentage reads mapped: 98.62
Strain: lineage4.1.1.3
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Tyr | missense_variant | 0.99 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.99 |
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 | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472714 | n.869A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472836 | n.991G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |