Run ID: ERR2229337
Sample name:
Date: 31-03-2023 17:02:13
Number of reads: 721600
Percentage reads mapped: 71.87
Strain: lineage4.8
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.31 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 490915 | p.Arg45Ser | missense_variant | 0.12 |
mshA | 575191 | c.-157C>A | upstream_gene_variant | 0.13 |
mshA | 576663 | p.Ala439Val | missense_variant | 0.12 |
mshA | 576750 | p.Lys468Thr | missense_variant | 0.15 |
rpoB | 761153 | c.1347G>A | synonymous_variant | 0.17 |
rpoC | 762524 | c.-846G>A | upstream_gene_variant | 0.13 |
rpoC | 766866 | p.Thr1166Asn | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775939 | p.Ala848Ser | missense_variant | 0.12 |
mmpL5 | 777167 | p.Phe438Leu | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1407517 | c.-177G>T | upstream_gene_variant | 0.12 |
atpE | 1460902 | c.-143A>G | upstream_gene_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476087 | n.2430C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.11 |
inhA | 1674505 | p.Gly102Trp | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102015 | p.Val343Asp | missense_variant | 0.14 |
katG | 2155813 | p.Pro100Leu | missense_variant | 0.12 |
PPE35 | 2168334 | p.Ser760Ile | missense_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169188 | c.1425C>T | synonymous_variant | 0.29 |
Rv1979c | 2223157 | p.Gly3Val | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289901 | c.-660G>T | upstream_gene_variant | 0.14 |
kasA | 2519224 | c.1110C>A | synonymous_variant | 0.29 |
folC | 2747574 | p.Pro9Thr | missense_variant | 0.12 |
fbiD | 3339357 | c.240G>T | synonymous_variant | 0.12 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
Rv3083 | 3448500 | c.-4A>G | upstream_gene_variant | 1.0 |
Rv3083 | 3448501 | c.-3G>T | upstream_gene_variant | 1.0 |
whiB7 | 3568683 | c.-4G>T | upstream_gene_variant | 0.12 |
Rv3236c | 3612553 | c.564G>T | synonymous_variant | 0.12 |
fbiA | 3640723 | p.Asp61Tyr | missense_variant | 0.12 |
panD | 4044117 | c.165G>T | synonymous_variant | 0.14 |
embC | 4241981 | p.Pro707Ser | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242854 | p.Gly998Cys | missense_variant | 0.13 |
embA | 4244851 | p.Arg540Leu | missense_variant | 0.15 |
embB | 4247318 | p.Ile269Phe | missense_variant | 0.11 |
embB | 4249733 | p.Pro1074Thr | missense_variant | 0.25 |
aftB | 4268267 | c.570G>T | synonymous_variant | 0.13 |
aftB | 4268726 | c.111G>T | synonymous_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |