Run ID: SRR5341295
Sample name:
Date: 04-04-2023 10:13:23
Number of reads: 2281347
Percentage reads mapped: 91.63
Strain: lineage1.2.2.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.98 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 0.96 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 0.93 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 0.99 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.98 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490666 | c.-117G>T | upstream_gene_variant | 0.91 |
fgd1 | 490678 | c.-105_-104insG | upstream_gene_variant | 0.85 |
fgd1 | 490687 | c.-96T>C | upstream_gene_variant | 0.86 |
fgd1 | 490689 | c.-94_-93delCCinsTG | upstream_gene_variant | 0.83 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.97 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.97 |
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 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.94 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472129 | n.284G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472253 | n.408G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472606 | n.761C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472645 | n.800G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472733 | n.888G>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472742 | n.897C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472969 | n.1125delC | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473054 | n.1209C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475687 | n.2030C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475880 | n.2223C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475881 | n.2224T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475882 | n.2225C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475895 | n.2238C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475920 | n.2263G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475924 | n.2267A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475933 | n.2276C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475939 | n.2282G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476242 | n.2585C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476265 | n.2608G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476427 | n.2770G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102240 | p.Arg268His | missense_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 0.96 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.91 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.98 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.99 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 0.92 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.98 |
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 | 0.96 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.96 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.95 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.99 |
embA | 4246345 | p.Arg1038His | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.93 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.98 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.96 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 0.97 |
ethA | 4326330 | p.Tyr382Asn | missense_variant | 0.99 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 1.0 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 0.91 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.93 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407715 | p.Lys163Thr | missense_variant | 0.98 |
gid | 4407848 | p.Ala119Thr | missense_variant | 0.95 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.96 |
gid | 4408443 | c.-241C>A | upstream_gene_variant | 0.99 |