Run ID: ERR4821538
Sample name:
Date: 01-04-2023 17:18:36
Number of reads: 647823
Percentage reads mapped: 80.19
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5821 | c.582G>T | synonymous_variant | 0.2 |
gyrB | 6924 | p.Phe562Ser | missense_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9479 | c.2179delA | frameshift_variant | 0.11 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576301 | c.954A>G | synonymous_variant | 0.14 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_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 |
mmpS5 | 778658 | p.Gly83Val | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800925 | c.119_120delGC | frameshift_variant | 0.13 |
rplC | 801235 | p.Ala143Thr | missense_variant | 0.15 |
fbiC | 1303271 | p.Leu114Pro | missense_variant | 0.14 |
fbiC | 1303338 | c.408C>A | synonymous_variant | 0.15 |
embR | 1416412 | c.936T>C | synonymous_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471781 | n.-65G>T | upstream_gene_variant | 0.15 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472386 | n.543delT | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473122 | n.1281delA | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474345 | n.688A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673984 | p.Ala182Asp | missense_variant | 0.22 |
fabG1 | 1674059 | p.Pro207Leu | missense_variant | 0.14 |
inhA | 1674129 | c.-73C>T | upstream_gene_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918549 | p.Arg204Cys | missense_variant | 0.12 |
ndh | 2102973 | p.Phe24Ile | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223210 | c.-47delG | upstream_gene_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
pncA | 2289456 | c.-215G>T | upstream_gene_variant | 0.15 |
eis | 2714898 | c.435C>A | synonymous_variant | 0.13 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2859428 | p.Pro331Ser | missense_variant | 0.12 |
pepQ | 2859549 | c.870C>T | synonymous_variant | 0.12 |
pepQ | 2860373 | p.Ala16Ser | missense_variant | 0.17 |
ribD | 2987562 | p.His242Tyr | missense_variant | 0.15 |
Rv2752c | 3065268 | c.924A>G | synonymous_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 1.0 |
ald | 3087000 | p.Ala61Ser | missense_variant | 0.22 |
Rv3083 | 3449870 | p.Ser456Tyr | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474694 | p.Leu230Met | missense_variant | 0.14 |
Rv3236c | 3612218 | p.Val300Ala | missense_variant | 0.11 |
fbiA | 3640717 | p.Cys59Arg | missense_variant | 0.15 |
fbiB | 3641112 | c.-423T>C | upstream_gene_variant | 0.11 |
fbiB | 3642500 | c.966C>A | synonymous_variant | 0.12 |
fbiB | 3642655 | p.Thr374Met | missense_variant | 0.12 |
fbiB | 3642877 | p.Lys448Arg | missense_variant | 1.0 |
clpC1 | 4038726 | p.Thr660Asn | missense_variant | 0.12 |
clpC1 | 4039605 | p.Glu367Val | missense_variant | 0.14 |
clpC1 | 4039805 | c.900C>A | synonymous_variant | 0.13 |
clpC1 | 4040446 | p.Val87Phe | missense_variant | 0.18 |
embC | 4240272 | c.413delC | frameshift_variant | 0.11 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243945 | p.Thr238Asn | missense_variant | 0.11 |
embA | 4245214 | p.Ala661Glu | missense_variant | 0.17 |
embA | 4245651 | p.Thr807Ala | missense_variant | 0.12 |
embB | 4246568 | p.Ala19Thr | missense_variant | 0.22 |
embB | 4247420 | p.Ile303Val | missense_variant | 0.12 |
embB | 4247522 | p.Leu337Met | missense_variant | 0.11 |
aftB | 4266999 | p.Cys613Ser | missense_variant | 0.17 |
aftB | 4267105 | p.Val578Leu | missense_variant | 0.12 |
aftB | 4268802 | p.Ala12Glu | missense_variant | 0.25 |
aftB | 4269213 | c.-377C>A | upstream_gene_variant | 0.14 |
ethA | 4326698 | p.Arg259Leu | missense_variant | 0.15 |
ethR | 4326700 | c.-849C>A | upstream_gene_variant | 0.15 |
ethR | 4327657 | p.Leu37Phe | missense_variant | 0.14 |
ethA | 4327827 | c.-354A>G | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |