Run ID: ERR2851355
Sample name:
Date: 31-03-2023 23:52:38
Number of reads: 115278
Percentage reads mapped: 66.68
Strain: lineage3
Drug-resistance: MDR-TB
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 | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4249583 | p.Asp1024Asn | missense_variant | 1.0 | ethambutol |
gid | 4407816 | c.386delG | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5769 | p.Pro177His | missense_variant | 0.2 |
gyrB | 6824 | p.Leu529Met | missense_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8414 | c.1113C>T | synonymous_variant | 1.0 |
gyrA | 9119 | c.1818A>G | synonymous_variant | 0.4 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9719 | c.2418G>T | synonymous_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.25 |
rpoB | 761934 | p.Gly710Ser | missense_variant | 0.22 |
rpoB | 762041 | p.His745Gln | missense_variant | 0.29 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 764345 | p.Pro326Thr | missense_variant | 0.18 |
rpoC | 764817 | p.Val483Ala | missense_variant | 1.0 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.5 |
rpoC | 765868 | c.2499G>T | synonymous_variant | 0.67 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777076 | p.Ala469Thr | missense_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304156 | p.Arg409Leu | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471981 | n.136C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472134 | n.289C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472247 | n.402C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472657 | n.812G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475278 | n.1621G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.33 |
inhA | 1674510 | p.Met103Ile | missense_variant | 0.67 |
rpsA | 1833563 | p.Ser8Pro | missense_variant | 0.5 |
rpsA | 1834456 | c.915T>A | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2170461 | p.Gly51Glu | missense_variant | 1.0 |
Rv1979c | 2221839 | c.1326T>C | synonymous_variant | 0.25 |
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 | 2517957 | c.-158G>T | upstream_gene_variant | 0.15 |
kasA | 2518531 | c.417G>T | synonymous_variant | 0.25 |
eis | 2714605 | p.Ala243Glu | missense_variant | 0.5 |
ahpC | 2726103 | c.-90G>A | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2860602 | c.-184A>G | upstream_gene_variant | 0.29 |
thyA | 3074620 | c.-149C>A | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087808 | p.Arg330Leu | missense_variant | 0.5 |
Rv3083 | 3449000 | p.Pro166Gln | missense_variant | 0.67 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840602 | c.819G>T | synonymous_variant | 0.4 |
embC | 4240142 | c.280C>T | synonymous_variant | 1.0 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4241355 | p.Gln498Arg | missense_variant | 0.4 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244213 | c.981C>A | synonymous_variant | 1.0 |
embB | 4249591 | c.3078C>T | synonymous_variant | 0.67 |
embB | 4249779 | p.Trp1089Leu | missense_variant | 0.33 |
ethA | 4326036 | p.Phe480Ile | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407666 | c.537C>A | synonymous_variant | 0.18 |