Run ID: ERR4817976
Sample name:
Date: 01-04-2023 15:17:53
Number of reads: 928843
Percentage reads mapped: 57.48
Strain: lineage4.1.2.1
Drug-resistance: HR-TB
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 | 0.91 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6828 | p.Met530Thr | missense_variant | 0.17 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9428 | p.Asp709Glu | missense_variant | 0.22 |
fgd1 | 491397 | p.Glu205Asp | missense_variant | 0.15 |
fgd1 | 491506 | p.Ala242Ser | missense_variant | 0.13 |
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 | 761027 | c.1221A>G | synonymous_variant | 0.14 |
rpoB | 762202 | p.Lys799Met | missense_variant | 0.14 |
rpoB | 762214 | c.2411delG | frameshift_variant | 0.13 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.11 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.11 |
rpoC | 764721 | p.Leu451Pro | missense_variant | 0.11 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.1 |
rpoC | 764740 | p.Met457Ile | missense_variant | 0.11 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.11 |
rpoC | 764762 | p.His465Tyr | missense_variant | 0.11 |
rpoC | 764776 | p.Ile469Met | missense_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775819 | p.Phe888Leu | missense_variant | 0.14 |
mmpL5 | 776086 | p.Val799Ile | missense_variant | 0.15 |
mmpL5 | 776617 | p.Pro622Ser | missense_variant | 0.15 |
mmpL5 | 777714 | p.Ile256Thr | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800804 | c.-5G>T | upstream_gene_variant | 0.17 |
rplC | 801363 | c.555C>T | synonymous_variant | 0.13 |
fbiC | 1302870 | c.-61G>A | upstream_gene_variant | 0.2 |
embR | 1416914 | p.Trp145* | stop_gained | 0.12 |
atpE | 1461153 | p.Ser37Pro | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472096 | n.251T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472100 | n.255T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472118 | n.273A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472279 | n.434T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472284 | n.439C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474783 | n.1126G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475772 | n.2115A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475897 | n.2240T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475938 | n.2281C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476520 | n.2863G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476539 | n.2882A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476544 | n.2887T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476547 | n.2890C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476563 | n.2906G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476566 | n.2909A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476595 | n.2938C>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476602 | n.2945G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476608 | n.2951C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476629 | n.2972C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673987 | p.Pro183Leu | missense_variant | 0.18 |
fabG1 | 1674061 | p.Ala208Ser | missense_variant | 0.15 |
rpsA | 1833363 | c.-179A>G | upstream_gene_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154166 | p.Ala649Val | missense_variant | 0.12 |
PPE35 | 2168467 | p.Leu716Phe | missense_variant | 0.2 |
PPE35 | 2170578 | p.Ser12Leu | missense_variant | 0.12 |
Rv1979c | 2222216 | p.Val317Phe | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289023 | c.219C>T | synonymous_variant | 0.14 |
pncA | 2289783 | c.-542G>A | upstream_gene_variant | 0.13 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087622 | p.Ala268Gly | missense_variant | 0.14 |
ald | 3087638 | c.819C>T | synonymous_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877558 | p.Pro317His | missense_variant | 0.12 |
rpoA | 3877718 | p.Leu264Ile | missense_variant | 0.14 |
rpoA | 3878307 | c.201C>A | synonymous_variant | 0.13 |
rpoA | 3878527 | c.-20C>A | upstream_gene_variant | 0.4 |
ddn | 3987205 | p.Glu121Gly | missense_variant | 0.1 |
clpC1 | 4038588 | p.Arg706His | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
aftB | 4266961 | p.Arg626Trp | missense_variant | 0.14 |
ubiA | 4269158 | p.Ala226Ser | missense_variant | 0.12 |
ethA | 4327367 | p.Glu36Val | missense_variant | 0.12 |
ethA | 4327482 | c.-9C>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |