Run ID: ERR4797047
Sample name:
Date: 01-04-2023 07:19:22
Number of reads: 3820925
Percentage reads mapped: 99.67
Strain: lineage2.2.1.1
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 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 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 |
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289031 | p.His71Tyr | missense_variant | 1.0 | pyrazinamide |
embA | 4243217 | c.-16C>G | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326231 | c.1242delT | frameshift_variant | 1.0 | ethionamide, 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 | 0.99 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.44 |
ccsA | 619725 | c.-166C>G | upstream_gene_variant | 0.12 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 762285 | p.Arg827Cys | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.25 |
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 |
Rv1258c | 1407489 | c.-149G>A | upstream_gene_variant | 0.13 |
embR | 1416878 | c.469delC | frameshift_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471793 | n.-53G>T | upstream_gene_variant | 0.33 |
rrs | 1471805 | n.-41C>A | upstream_gene_variant | 0.75 |
rrl | 1474574 | n.917A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476058 | n.2401T>G | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.3 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102817 | p.Leu76Val | missense_variant | 0.25 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168693 | p.Asn640Lys | missense_variant | 0.15 |
PPE35 | 2170390 | p.Trp75Gly | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.23 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.2 |
Rv2752c | 3065090 | c.1101delA | frameshift_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339273 | c.156T>A | synonymous_variant | 0.11 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474213 | p.Lys69Asn | missense_variant | 0.14 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
clpC1 | 4040240 | c.465C>A | synonymous_variant | 0.5 |
clpC1 | 4040295 | p.Gln137Pro | missense_variant | 0.25 |
embC | 4242131 | p.Val757Leu | missense_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245835 | p.Leu868Arg | missense_variant | 0.22 |
embA | 4246143 | p.Ile971Phe | missense_variant | 0.25 |
embB | 4247100 | p.Ala196Val | missense_variant | 0.12 |
embB | 4247424 | p.Leu304Pro | missense_variant | 0.15 |
embB | 4247880 | p.Val456Ala | missense_variant | 1.0 |
embB | 4248115 | c.1602C>T | synonymous_variant | 0.98 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267902 | p.Val312Gly | missense_variant | 0.43 |
aftB | 4267930 | p.Arg303Gly | missense_variant | 0.12 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.31 |
ethA | 4326271 | c.1203T>C | synonymous_variant | 0.1 |
whiB6 | 4338323 | c.198dupC | frameshift_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 |