Run ID: ERR4817102
Sample name:
Date: 01-04-2023 14:48:10
Number of reads: 212234
Percentage reads mapped: 9.68
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | 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 |
gyrB | 6124 | c.885C>T | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7792 | p.Thr164Met | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 9047 | c.1746C>T | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9443 | c.2142G>A | synonymous_variant | 1.0 |
mshA | 576000 | p.Asp218Ala | missense_variant | 1.0 |
rpoB | 760070 | c.264T>C | synonymous_variant | 0.25 |
rpoB | 760490 | c.684C>T | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763848 | p.Lys160Arg | missense_variant | 0.18 |
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 | 766197 | p.Asp943Gly | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776395 | p.Phe696Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781700 | c.141G>A | synonymous_variant | 0.4 |
fbiC | 1303013 | p.Arg28Leu | missense_variant | 0.33 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472215 | n.370A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472234 | n.389T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472256 | n.411T>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472263 | n.418C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472700 | n.855C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472705 | n.860G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472928 | n.1083A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473029 | n.1184C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473061 | n.1216T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473089 | n.1244A>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473094 | n.1249T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473115 | n.1270G>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473127 | n.1282G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473147 | n.1302G>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476353 | n.2696G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_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 | 1.0 |
pncA | 2290109 | c.-868C>T | upstream_gene_variant | 0.4 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519183 | c.1070dupT | frameshift_variant | 0.25 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726150 | c.-43G>A | upstream_gene_variant | 0.33 |
folC | 2747156 | p.Ala148Val | missense_variant | 0.25 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474787 | p.Arg261Cys | missense_variant | 0.22 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fbiB | 3641678 | c.144T>C | synonymous_variant | 0.5 |
rpoA | 3877545 | c.963G>A | synonymous_variant | 0.33 |
rpoA | 3877554 | c.954G>T | synonymous_variant | 1.0 |
ddn | 3987057 | p.Arg72Trp | missense_variant | 1.0 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
embC | 4240074 | p.Glu71Gly | missense_variant | 0.15 |
embC | 4240535 | p.Ser225Arg | 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 | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248571 | c.2058G>T | synonymous_variant | 0.22 |
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 | 4407873 | c.330G>T | synonymous_variant | 1.0 |