Run ID: ERR4820265
Sample name:
Date: 01-04-2023 16:34:54
Number of reads: 1275382
Percentage reads mapped: 79.02
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | 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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.75 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.11 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.21 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.23 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.23 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.24 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.24 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.23 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.22 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.24 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.35 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.32 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.32 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.3 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.25 |
rpoC | 763109 | c.-261C>T | upstream_gene_variant | 0.22 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.19 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.19 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.13 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.12 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.17 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.18 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.19 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.16 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.12 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.12 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.12 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.12 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.12 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.11 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.11 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.12 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.12 |
rpoC | 764015 | c.646C>T | synonymous_variant | 0.12 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.13 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.11 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.13 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.11 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.1 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.17 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.17 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.17 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.21 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.14 |
rpoC | 764780 | p.Ser471Ala | missense_variant | 0.12 |
rpoC | 764793 | p.Met475Lys | missense_variant | 0.12 |
rpoC | 764797 | c.1428G>T | synonymous_variant | 0.11 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.11 |
rpoC | 764813 | p.Gln482Glu | missense_variant | 0.11 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766551 | p.Phe1061Tyr | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417068 | c.280T>C | synonymous_variant | 0.12 |
embR | 1417402 | c.-55A>G | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473122 | n.1281delA | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473262 | n.1417T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.25 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474732 | n.1075A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474783 | n.1126G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475694 | n.2038_2039insACG | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475697 | n.2040C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475707 | n.2050T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475785 | n.2128A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.5 |
inhA | 1674356 | p.Asp52Gly | missense_variant | 0.12 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.14 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.14 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 0.14 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.14 |
rpsA | 1834186 | c.645C>G | synonymous_variant | 0.11 |
rpsA | 1834189 | c.648G>T | synonymous_variant | 0.1 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.15 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.15 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.16 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.16 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.18 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.27 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.28 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.21 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.21 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.19 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.16 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.14 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.14 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.12 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155272 | c.840G>A | synonymous_variant | 0.17 |
PPE35 | 2168163 | p.Pro817Leu | missense_variant | 0.11 |
Rv1979c | 2222127 | c.1038C>T | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
folC | 2746704 | p.Ala299Ser | missense_variant | 0.12 |
folC | 2747702 | c.-104T>C | upstream_gene_variant | 0.1 |
Rv2752c | 3065424 | c.768C>T | synonymous_variant | 0.14 |
Rv2752c | 3065535 | c.656delG | frameshift_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474081 | c.75C>G | synonymous_variant | 0.1 |
Rv3236c | 3612926 | c.190delA | frameshift_variant | 0.11 |
fbiA | 3640363 | c.-180C>G | upstream_gene_variant | 0.11 |
clpC1 | 4039098 | p.Arg536Pro | missense_variant | 0.1 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.12 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |