Run ID: ERR5336160
Sample name:
Date: 01-04-2023 22:32:28
Number of reads: 2596928
Percentage reads mapped: 68.82
Strain: lineage6.3.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage6 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
lineage6.3 | West-Africa 2 | AFRI_1 | RD702 | 1.0 |
lineage6.3.2 | West-Africa 2 | AFRI_1 | RD702 | 0.99 |
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 | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | 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 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.36 |
rpoB | 760969 | p.Ser388Leu | missense_variant | 1.0 |
rpoB | 761723 | p.Glu639Asp | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_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 |
atpE | 1461251 | c.207G>T | synonymous_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472118 | n.273A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472506 | n.661A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474425 | n.768A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474428 | n.771C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.23 |
inhA | 1674434 | p.Val78Ala | missense_variant | 1.0 |
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 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.14 |
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 |
Rv2752c | 3065508 | c.684T>G | synonymous_variant | 1.0 |
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 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.17 |
Rv3083 | 3449781 | c.1278G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiA | 3640753 | p.Gly71Ser | missense_variant | 1.0 |
rpoA | 3877696 | p.Thr271Ile | missense_variant | 1.0 |
rpoA | 3878567 | c.-60C>G | upstream_gene_variant | 0.16 |
clpC1 | 4038442 | p.Ala755Thr | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241843 | p.Leu661Ile | missense_variant | 0.97 |
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 | 0.99 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.21 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.21 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.21 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.2 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.2 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.21 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4268186 | c.651C>T | synonymous_variant | 1.0 |
aftB | 4268477 | c.360C>T | synonymous_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 |
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 |