Run ID: ERR4818574
Sample name:
Date: 01-04-2023 15:38:08
Number of reads: 745553
Percentage reads mapped: 89.59
Strain: lineage6
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage6 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.25 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.47 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.3 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.18 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 6934 | c.-368A>G | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8493 | p.Leu398Phe | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.24 |
fgd1 | 491668 | p.Lys296Glu | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575231 | c.-117G>A | upstream_gene_variant | 0.12 |
mshA | 576157 | c.810C>T | synonymous_variant | 0.17 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.5 |
rpoB | 760855 | p.Thr350Ile | missense_variant | 1.0 |
rpoB | 760969 | p.Ser388Leu | missense_variant | 1.0 |
rpoB | 761723 | p.Glu639Asp | missense_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.11 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.16 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.15 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.19 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766231 | c.2862T>C | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
Rv1258c | 1406685 | p.Val219Ala | missense_variant | 1.0 |
embR | 1416633 | p.Leu239Val | missense_variant | 1.0 |
atpE | 1461251 | c.207G>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473122 | n.1278A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474413 | n.757_776delCCCACACGCGCATACGCGCG | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474437 | n.781_782delAA | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475757 | n.2101_2104delACCC | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.2 |
inhA | 1674434 | p.Val78Ala | missense_variant | 1.0 |
rpsA | 1834030 | c.489C>T | synonymous_variant | 0.12 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.13 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.12 |
rpsA | 1834043 | p.Glu168Gln | missense_variant | 0.13 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.13 |
rpsA | 1834054 | c.513C>T | synonymous_variant | 0.14 |
rpsA | 1834090 | c.549G>T | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.11 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.13 |
PPE35 | 2169581 | c.1032C>G | synonymous_variant | 0.15 |
PPE35 | 2169587 | c.1026G>A | synonymous_variant | 0.16 |
PPE35 | 2170190 | p.Glu141Asp | missense_variant | 0.13 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289858 | c.-617G>T | upstream_gene_variant | 0.17 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.2 |
ahpC | 2726449 | p.Ser86Trp | missense_variant | 0.11 |
pepQ | 2859920 | p.Arg167* | stop_gained | 0.13 |
thyA | 3074262 | c.210T>C | synonymous_variant | 0.22 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
Rv3083 | 3449396 | p.Cys298Tyr | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
Rv3236c | 3612143 | p.Arg325His | missense_variant | 1.0 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.17 |
panD | 4044432 | c.-151T>G | upstream_gene_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241713 | c.1851G>A | synonymous_variant | 0.2 |
embC | 4241715 | p.Asn618Thr | missense_variant | 0.22 |
embC | 4241720 | p.Thr620Ser | missense_variant | 0.22 |
embC | 4241723 | c.1862delT | frameshift_variant | 0.25 |
embC | 4241727 | c.1867_1868delGC | frameshift_variant | 0.25 |
embC | 4241843 | p.Leu661Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embA | 4244379 | p.Pro383Ser | missense_variant | 1.0 |
embA | 4245351 | p.Lys707Glu | missense_variant | 0.14 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247427 | p.Gly305Ala | missense_variant | 0.1 |
embB | 4247437 | c.924A>G | synonymous_variant | 0.11 |
embB | 4247440 | c.927C>G | synonymous_variant | 0.11 |
embB | 4247441 | p.Ala310Ser | missense_variant | 0.12 |
embB | 4247446 | p.Asp311Glu | missense_variant | 0.12 |
embB | 4247449 | c.936C>T | synonymous_variant | 0.12 |
embB | 4247452 | c.939C>G | synonymous_variant | 0.12 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269522 | c.-686C>T | upstream_gene_variant | 0.92 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
aftB | 4269693 | c.-857C>T | upstream_gene_variant | 1.0 |
ethA | 4326465 | p.Ile337Val | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408034 | p.Glu57Lys | missense_variant | 1.0 |