Run ID: ERR181750
Sample name:
Date: 31-03-2023 15:18:23
Number of reads: 1715673
Percentage reads mapped: 60.57
Strain: lineage1.1.3.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.96 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.95 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 0.96 |
lineage1.1.3.2 | Indo-Oceanic | NA | RD239 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.93 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8188 | p.Leu296Pro | missense_variant | 0.97 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.91 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.98 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.91 |
ccsA | 619695 | c.-196G>A | upstream_gene_variant | 0.97 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.97 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.98 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.98 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.14 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.17 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.17 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.16 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.17 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.17 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.18 |
rpoC | 764579 | p.Asp404His | missense_variant | 0.18 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.17 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.17 |
rpoC | 764599 | c.1230G>A | synonymous_variant | 0.16 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.17 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.17 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 1.0 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 0.96 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.97 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801166 | p.Gly120Ser | missense_variant | 0.95 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.25 |
fbiC | 1304159 | p.Val410Gly | missense_variant | 0.19 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.95 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472100 | n.255T>C | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472256 | n.411T>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472733 | n.888G>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472742 | n.897C>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473147 | n.1302G>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473179 | n.1334C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474927 | n.1271delC | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474931 | n.1274G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475843 | n.2186G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475849 | n.2192G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475853 | n.2196C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.31 |
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>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476621 | n.2964C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476624 | n.2967T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476637 | n.2980C>G | non_coding_transcript_exon_variant | 0.17 |
inhA | 1674883 | p.Ile228Val | missense_variant | 0.97 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.87 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.97 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.97 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.98 |
eis | 2714569 | p.Ala255Gly | missense_variant | 0.32 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.93 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.19 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.97 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.97 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.98 |
fbiB | 3642173 | c.639G>A | synonymous_variant | 0.91 |
rpoA | 3878630 | c.-123G>C | upstream_gene_variant | 0.12 |
rpoA | 3878687 | c.-180A>C | upstream_gene_variant | 0.91 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.26 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.96 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.95 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.92 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243848 | p.Val206Met | missense_variant | 0.97 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.95 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.92 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.93 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.95 |
ethA | 4328212 | c.-740delC | upstream_gene_variant | 0.9 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.97 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.95 |
gid | 4407780 | c.423G>A | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.94 |