Run ID: ERR4819224
Sample name:
Date: 01-04-2023 15:59:35
Number of reads: 1587499
Percentage reads mapped: 87.6
Strain: lineage1.2.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 1.0 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 1.0 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.79 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 6310 | c.-992G>T | upstream_gene_variant | 0.13 |
gyrB | 7008 | p.Leu590Pro | missense_variant | 0.15 |
gyrA | 7355 | c.54T>C | synonymous_variant | 0.1 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
rpoB | 761862 | p.Ala686Thr | missense_variant | 0.12 |
rpoB | 761889 | p.Val695Met | missense_variant | 0.11 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.11 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.13 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.13 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.12 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.13 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.14 |
rpoB | 763077 | p.Val1091Ile | missense_variant | 0.16 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.19 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.19 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.18 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.21 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.21 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764809 | c.1440C>T | 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 | 1302821 | c.-110G>A | upstream_gene_variant | 1.0 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472611 | n.766G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474635 | n.979_982delACCG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475697 | n.2040C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.3 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
inhA | 1674479 | p.His93Leu | missense_variant | 0.12 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.14 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.16 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.16 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.14 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.12 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.12 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.12 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168103 | p.Pro837Leu | missense_variant | 0.11 |
PPE35 | 2168506 | p.Gly703Cys | missense_variant | 0.2 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222750 | c.415C>T | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ribD | 2986947 | p.Asp37Asn | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338639 | c.-118T>C | upstream_gene_variant | 0.1 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |