Run ID: SRR21240243
Sample name:
Date: 04-04-2023 00:13:07
Number of reads: 1215878
Percentage reads mapped: 86.76
Strain: lineage4.3.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.2 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9431 | c.2130G>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.33 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.16 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406630 | c.711G>T | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475927 | n.2270G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.34 |
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 | 0.32 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102308 | c.735G>A | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449854 | p.Met451Val | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878630 | c.-123G>C | upstream_gene_variant | 0.13 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.96 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |