Run ID: ERR2514389
Sample name:
Date: 31-03-2023 20:18:26
Number of reads: 394432
Percentage reads mapped: 94.01
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 | 5192 | c.-48C>T | upstream_gene_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.22 |
rpoB | 759711 | c.-95_-88delGCCGAAAC | upstream_gene_variant | 0.33 |
rpoB | 759723 | c.-84C>T | upstream_gene_variant | 0.33 |
rpoB | 759726 | c.-81A>T | upstream_gene_variant | 0.33 |
rpoB | 759727 | c.-80A>T | upstream_gene_variant | 0.33 |
rpoB | 759730 | c.-77A>G | upstream_gene_variant | 0.33 |
rpoB | 759733 | c.-74_-73insGTTTCGGC | upstream_gene_variant | 0.4 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762521 | c.-849C>T | upstream_gene_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766582 | c.3213C>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776872 | p.Glu537Lys | missense_variant | 0.15 |
mmpL5 | 777482 | c.999G>A | synonymous_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304901 | c.1971C>G | synonymous_variant | 0.29 |
fbiC | 1305463 | p.Arg845Cys | missense_variant | 0.14 |
Rv1258c | 1406147 | c.1194C>G | synonymous_variant | 0.25 |
embR | 1416772 | c.576C>A | synonymous_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471701 | n.-145A>G | upstream_gene_variant | 0.12 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473291 | n.1446G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476630 | n.2973A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.29 |
rpsA | 1834157 | c.616T>C | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102841 | p.Ile68Phe | missense_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154914 | p.His400Tyr | missense_variant | 0.2 |
katG | 2155672 | p.Leu147Pro | missense_variant | 0.25 |
katG | 2155919 | c.190_192delTAT | conservative_inframe_deletion | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.13 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.12 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.2 |
PPE35 | 2170424 | c.189G>C | synonymous_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.12 |
kasA | 2518816 | c.702C>A | synonymous_variant | 0.11 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.11 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.11 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.11 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.11 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.12 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.12 |
kasA | 2518888 | c.774C>T | synonymous_variant | 0.12 |
kasA | 2518898 | c.784T>C | synonymous_variant | 0.14 |
kasA | 2518906 | c.792A>G | synonymous_variant | 0.13 |
kasA | 2518910 | p.Leu266Met | missense_variant | 0.13 |
kasA | 2519153 | p.Ile347Val | missense_variant | 0.67 |
eis | 2714569 | p.Ala255Gly | missense_variant | 0.22 |
eis | 2715019 | p.His105Arg | missense_variant | 0.15 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726265 | p.Lys25Gln | missense_variant | 0.23 |
thyA | 3074645 | c.-174T>G | upstream_gene_variant | 0.33 |
thyA | 3074648 | c.-177T>G | upstream_gene_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448514 | p.His4Leu | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.25 |
clpC1 | 4039916 | c.789T>G | synonymous_variant | 0.25 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245610 | p.Val793Ala | missense_variant | 0.22 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.11 |
ethA | 4326496 | c.978G>A | synonymous_variant | 0.1 |
whiB6 | 4338485 | p.Asn13Tyr | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |