Run ID: SRR9971163
Sample name:
Date: 04-04-2023 23:14:09
Number of reads: 1787070
Percentage reads mapped: 37.86
Strain: lineage4.4.1.1.1
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 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
lineage4.4.1.1.1 | Euro-American | S;Orphans | None | 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 |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.59 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289142 | p.Tyr34Asp | 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 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.19 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.1 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.1 |
rpoC | 764577 | p.Ser403Cys | missense_variant | 0.1 |
rpoC | 766487 | p.Pro1040Ser | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1461048 | p.Asp2Asn | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472301 | n.456C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472317 | n.472G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473265 | n.1420C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473664 | n.7G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476354 | n.2697A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476388 | n.2731T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476428 | n.2771C>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.65 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.23 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064993 | p.Trp400* | stop_gained | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339287 | p.Arg57Leu | missense_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.5 |
Rv3083 | 3448482 | c.-22G>T | upstream_gene_variant | 0.13 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.98 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.23 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.21 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.22 |
ubiA | 4269308 | p.Phe176Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |