Run ID: SRR21595948
Sample name:
Date: 04-04-2023 02:17:17
Number of reads: 558767
Percentage reads mapped: 94.94
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 619807 | c.-84G>T | upstream_gene_variant | 0.11 |
ccsA | 620562 | c.672C>A | synonymous_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | 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 | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473149 | n.1304G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674971 | p.Ile257Thr | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102227 | c.816C>A | synonymous_variant | 0.11 |
PPE35 | 2168468 | c.2145C>T | synonymous_variant | 0.15 |
Rv1979c | 2222796 | c.369C>T | synonymous_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714559 | c.774C>T | synonymous_variant | 0.14 |
ahpC | 2726245 | p.Leu18Pro | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.22 |
rpoA | 3878185 | p.Gly108Val | missense_variant | 1.0 |
clpC1 | 4040621 | c.84C>T | synonymous_variant | 0.11 |
embC | 4239876 | p.Ala5Asp | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4246529 | p.Ser6Arg | missense_variant | 0.29 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.67 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.22 |
embB | 4248319 | c.1806A>T | synonymous_variant | 0.18 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.21 |
ethR | 4328024 | p.Arg159Gln | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |