Run ID: ERR1665405
Sample name:
Date: 31-03-2023 14:55:06
Number of reads: 2308038
Percentage reads mapped: 95.87
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpoB | 762089 | p.Glu761Asp | missense_variant | 1.0 | rifampicin |
rrs | 1472362 | n.517C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.16 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289207 | p.Asp12Gly | missense_variant | 1.0 | pyrazinamide |
eis | 2715369 | c.-37G>T | upstream_gene_variant | 1.0 | kanamycin |
embB | 4247574 | p.Asp354Ala | missense_variant | 0.99 | ethambutol |
embB | 4249583 | p.Asp1024Asn | missense_variant | 1.0 | ethambutol |
ethA | 4327480 | c.-7T>C | upstream_gene_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474674 | n.1017A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474675 | n.1018C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474694 | n.1037C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474732 | n.1075A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474783 | n.1126G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.1 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338563 | c.-42G>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |