Run ID: ERR5865299
Sample name:
Date: 01-04-2023 23:55:45
Number of reads: 2219743
Percentage reads mapped: 99.57
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
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 |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
pncA | 2289031 | p.His71Tyr | missense_variant | 1.0 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5892 | p.Val218Asp | missense_variant | 0.12 |
gyrB | 6626 | p.Ala463Pro | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7810 | c.513delC | frameshift_variant | 0.12 |
gyrA | 9196 | p.Val632Glu | missense_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575167 | c.-181G>A | upstream_gene_variant | 0.25 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760210 | p.Asn135Ser | missense_variant | 0.11 |
rpoB | 760337 | c.535delG | frameshift_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763641 | p.Arg91Leu | missense_variant | 0.13 |
rpoC | 764936 | p.Gln523Lys | missense_variant | 1.0 |
rpoC | 766120 | c.2751A>G | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777033 | c.1447delG | frameshift_variant | 0.12 |
mmpL5 | 777800 | c.681C>A | synonymous_variant | 0.12 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304204 | p.Ala425Asp | missense_variant | 0.29 |
Rv1258c | 1406323 | p.Ala340Thr | missense_variant | 0.11 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472291 | n.446G>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472899 | n.1055delG | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472931 | n.1089delC | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475930 | n.2273G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476226 | n.2569G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476431 | n.2774G>A | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476663 | n.3006C>A | non_coding_transcript_exon_variant | 0.2 |
rpsA | 1834032 | p.Tyr164Phe | missense_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834630 | c.1090delC | frameshift_variant | 0.11 |
tlyA | 1917769 | c.-171C>G | upstream_gene_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102861 | p.Gly61Glu | missense_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155168 | p.Ser315Ala | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2221822 | p.Ser448* | stop_gained | 0.12 |
Rv1979c | 2222167 | p.Ser333Ile | missense_variant | 0.2 |
Rv1979c | 2223025 | p.Ala47Glu | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289333 | c.-93dupT | upstream_gene_variant | 0.11 |
eis | 2714194 | p.Ser380Tyr | missense_variant | 0.11 |
eis | 2714296 | p.Ala346Glu | missense_variant | 0.14 |
ahpC | 2726748 | p.Asp186Asn | missense_variant | 0.12 |
folC | 2746197 | p.Ile468Val | missense_variant | 0.11 |
folC | 2746238 | p.Pro454Gln | missense_variant | 0.12 |
folC | 2747777 | c.-179C>G | upstream_gene_variant | 0.11 |
pepQ | 2859321 | c.1098C>A | synonymous_variant | 0.13 |
pepQ | 2860255 | p.Ala55Asp | missense_variant | 0.13 |
ribD | 2987242 | p.Arg135Gln | missense_variant | 0.12 |
thyX | 3067285 | p.Ala221Thr | missense_variant | 0.15 |
thyA | 3074490 | c.-19G>T | upstream_gene_variant | 0.12 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087638 | c.819C>A | synonymous_variant | 0.12 |
fbiD | 3338961 | c.-157G>A | upstream_gene_variant | 0.12 |
Rv3083 | 3448356 | c.-148G>A | upstream_gene_variant | 0.18 |
fprA | 3473821 | c.-186C>A | upstream_gene_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474788 | c.785delC | frameshift_variant | 0.12 |
fprA | 3475101 | c.1095C>A | synonymous_variant | 0.12 |
Rv3236c | 3612713 | p.Arg135Gln | missense_variant | 0.22 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3640755 | c.-780C>G | upstream_gene_variant | 0.17 |
fbiB | 3642769 | p.Leu412Arg | missense_variant | 0.14 |
alr | 3841589 | c.-169C>T | upstream_gene_variant | 0.11 |
ddn | 3986822 | c.-21delT | upstream_gene_variant | 0.11 |
ddn | 3987029 | c.186C>T | synonymous_variant | 0.17 |
clpC1 | 4039300 | p.Arg469Ser | missense_variant | 0.25 |
panD | 4044325 | c.-44C>T | upstream_gene_variant | 0.11 |
embC | 4240248 | p.Asp129Gly | missense_variant | 0.11 |
embC | 4242295 | p.Asp811Glu | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242648 | p.Leu929Arg | missense_variant | 0.11 |
embA | 4243317 | p.Gly29Asn | missense_variant | 0.14 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4246726 | c.213G>A | synonymous_variant | 1.0 |
embB | 4247491 | c.978G>T | synonymous_variant | 0.11 |
embB | 4249112 | p.Lys867Glu | missense_variant | 0.15 |
aftB | 4267119 | p.Ala573Val | missense_variant | 0.12 |
aftB | 4267207 | p.Val544Leu | missense_variant | 0.1 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethR | 4327648 | p.Glu34* | stop_gained | 0.15 |
whiB6 | 4338371 | p.Thr51Pro | 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 |