Run ID: ERR4821011
Sample name:
Date: 01-04-2023 17:00:45
Number of reads: 325732
Percentage reads mapped: 67.62
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 | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.74 | streptomycin |
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 | 491668 | p.Lys296Glu | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
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 | 762143 | c.2337T>C | synonymous_variant | 0.2 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.22 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.2 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.2 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.25 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.25 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.25 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.25 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.29 |
rpoB | 762426 | p.Ser874Pro | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763747 | c.380delA | frameshift_variant | 0.22 |
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 | 1471729 | n.-117T>C | upstream_gene_variant | 0.2 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472997 | n.1152G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473293 | n.1449delA | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.67 |
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 | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.4 |
fabG1 | 1673743 | p.Glu102Lys | missense_variant | 0.22 |
inhA | 1674434 | p.Val78Ala | missense_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.22 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.44 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.44 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.25 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.25 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.33 |
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 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168137 | p.Ile826Val | missense_variant | 0.2 |
PPE35 | 2168452 | c.2158_2160delGTC | conservative_inframe_deletion | 0.14 |
PPE35 | 2169461 | c.1151delT | frameshift_variant | 0.22 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518786 | p.Glu224Asp | missense_variant | 0.22 |
folC | 2747425 | c.174C>T | synonymous_variant | 0.4 |
pepQ | 2860570 | c.-152A>G | upstream_gene_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 |
Rv3236c | 3612750 | c.366delC | frameshift_variant | 0.22 |
alr | 3841495 | c.-75G>T | upstream_gene_variant | 0.13 |
panD | 4044341 | c.-60C>T | upstream_gene_variant | 0.17 |
panD | 4044432 | c.-151T>G | upstream_gene_variant | 1.0 |
embC | 4241120 | p.Ser420Arg | missense_variant | 0.5 |
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 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
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 | 1.0 |
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 |
gid | 4408090 | p.Pro38Leu | missense_variant | 0.22 |