Run ID: SRR5341306
Sample name:
Date: 04-04-2023 10:14:01
Number of reads: 6023637
Percentage reads mapped: 89.28
Strain: lineage4.4
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.95 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.98 | rifampicin |
rpoC | 765572 | p.Asp735Asn | missense_variant | 1.0 | rifampicin |
rrs | 1472723 | n.878G>A | non_coding_transcript_exon_variant | 0.76 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.18 | streptomycin |
embB | 4247431 | p.Met306Ile | missense_variant | 0.98 | ethambutol |
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 |
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 | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472489 | n.644A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476108 | n.2451T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2153924 | p.Lys730Glu | missense_variant | 1.0 |
katG | 2154226 | p.Gly629Ala | missense_variant | 1.0 |
PPE35 | 2170558 | p.Ala19Pro | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714523 | p.His270Gln | missense_variant | 0.98 |
Rv2752c | 3065715 | c.477T>C | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243324 | p.Val31Ala | missense_variant | 1.0 |
embB | 4247548 | c.1035C>T | synonymous_variant | 1.0 |
aftB | 4268928 | c.-92C>T | upstream_gene_variant | 0.99 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 0.99 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338599 | c.-78A>C | upstream_gene_variant | 1.0 |