Run ID: ERR4829313
Sample name:
Date: 01-04-2023 19:24:26
Number of reads: 3515788
Percentage reads mapped: 93.16
Strain: lineage4.8
Drug-resistance: Pre-XDR-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 |
---|---|---|---|---|---|
gyrA | 7581 | p.Asp94Asn | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761110 | p.Asp435Val | missense_variant | 0.99 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.57 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.88 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289073 | p.His57Tyr | missense_variant | 1.0 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779127 | c.139dupG | frameshift_variant | 0.88 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407495 | c.-155C>T | upstream_gene_variant | 0.16 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156424 | c.-313T>C | upstream_gene_variant | 0.23 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
fbiB | 3640974 | c.-561T>G | upstream_gene_variant | 1.0 |
rpoA | 3878582 | c.-75C>A | upstream_gene_variant | 1.0 |
embC | 4241699 | p.Met613Val | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.28 |
whiB6 | 4338234 | c.288A>G | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |