Run ID: ERR736879
Sample name:
Date: 02-04-2023 04:22:24
Number of reads: 3819748
Percentage reads mapped: 69.94
Strain: lineage1.1.3.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 1.0 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 1.0 |
lineage1.1.3.2 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 6994 | c.-308C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8188 | p.Leu296Pro | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576093 | p.Pro249Leu | missense_variant | 1.0 |
ccsA | 619695 | c.-196G>A | upstream_gene_variant | 0.99 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765230 | p.Ala621Thr | missense_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 |
rplC | 801166 | p.Gly120Ser | missense_variant | 0.99 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472574 | n.729T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473147 | n.1302G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473179 | n.1334C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474800 | n.1143T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476595 | n.2938C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476602 | n.2945G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476608 | n.2951C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476637 | n.2980C>G | non_coding_transcript_exon_variant | 0.18 |
inhA | 1674883 | p.Ile228Val | missense_variant | 1.0 |
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 | 2167983 | p.Gly877Asp | missense_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.98 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474381 | c.375C>G | synonymous_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiB | 3642173 | c.639G>A | synonymous_variant | 1.0 |
rpoA | 3878687 | c.-180A>C | upstream_gene_variant | 1.0 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.15 |
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 | 4243848 | p.Val206Met | missense_variant | 0.99 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.99 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407780 | c.423G>A | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |