Run ID: ERR4796348
Sample name:
Date: 01-04-2023 06:48:36
Number of reads: 2604546
Percentage reads mapped: 85.37
Strain: lineage2.2.1.2
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 |
lineage2.2.1.2 | East-Asian (Beijing) | Beijing-RD142 | RD105;RD207;RD181;RD142 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7510 | p.His70Arg | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288835 | p.Asp136Gly | missense_variant | 1.0 | pyrazinamide |
folC | 2747471 | p.Ile43Thr | missense_variant | 1.0 | para-aminosalicylic_acid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
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 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.32 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.37 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.26 |
ccsA | 620625 | p.Ile245Met | missense_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 |
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 | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472682 | n.839_843delGGGAT | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472698 | n.853A>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473640 | n.-18C>A | upstream_gene_variant | 0.19 |
rrl | 1474398 | n.742delG | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476573 | n.2916A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102312 | c.730dupC | frameshift_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.31 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.19 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.39 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.2 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.27 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4327472 | c.2T>C | start_lost | 1.0 |
whiB6 | 4338233 | p.Ser97Pro | missense_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 |