Run ID: SRR13180246
Sample name:
Date: 03-04-2023 08:15:14
Number of reads: 1931311
Percentage reads mapped: 91.15
Strain: lineage4.8
Drug-resistance: HR-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 |
---|---|---|---|---|---|
katG | 2145477 | c.-419_*8411del | transcript_ablation | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5758 | p.Phe173Leu | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407356 | c.-16T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
rpoA | 3878530 | c.-23C>T | upstream_gene_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_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 |