Run ID: SRR6257052
Sample name:
Date: 04-04-2023 13:24:29
Number of reads: 475918
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 | 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 |
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 |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288719 | p.Met175Val | missense_variant | 0.12 | pyrazinamide |
pncA | 2288928 | p.Gly105Asp | missense_variant | 1.0 | pyrazinamide |
embB | 4247399 | p.Asn296His | missense_variant | 1.0 | ethambutol |
ethA | 4327363 | c.110delA | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5990 | p.Phe251Leu | missense_variant | 0.18 |
gyrB | 7082 | p.Glu615Lys | missense_variant | 0.11 |
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 | 576662 | p.Ala439Pro | missense_variant | 0.17 |
mshA | 576695 | p.Ala450Thr | missense_variant | 0.18 |
ccsA | 619787 | c.-104T>A | upstream_gene_variant | 0.11 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 763026 | p.Gly1074Cys | missense_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 767243 | p.Tyr1292Asn | missense_variant | 0.11 |
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 | 776424 | p.Asp686Gly | missense_variant | 0.13 |
mmpL5 | 778312 | p.Gly57Arg | missense_variant | 0.13 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302822 | c.-109T>G | upstream_gene_variant | 0.13 |
fbiC | 1304887 | p.Leu653Met | missense_variant | 0.11 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673406 | c.-796C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673810 | p.Ser124Leu | missense_variant | 0.12 |
rpsA | 1833623 | p.Lys28Glu | missense_variant | 0.14 |
rpsA | 1834007 | p.Arg156Cys | missense_variant | 0.15 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834249 | p.His236Gln | missense_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918417 | c.478T>C | synonymous_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155938 | p.Met58Ile | missense_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168448 | c.2164delC | frameshift_variant | 0.11 |
PPE35 | 2168863 | p.Leu584Met | missense_variant | 0.15 |
PPE35 | 2170511 | c.102G>A | synonymous_variant | 0.12 |
Rv1979c | 2223034 | p.Gly44Val | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747249 | p.Pro117Leu | missense_variant | 0.15 |
thyA | 3074567 | c.-96C>A | 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 | 3087311 | c.494dupG | frameshift_variant | 1.0 |
fbiD | 3339520 | p.His135Asp | missense_variant | 0.17 |
Rv3083 | 3449304 | c.801A>G | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641161 | p.Asp207Tyr | missense_variant | 0.17 |
alr | 3840464 | p.Phe319Leu | missense_variant | 0.13 |
alr | 3840934 | p.Asn163Asp | missense_variant | 0.1 |
rpoA | 3877850 | p.Gly220Ser | missense_variant | 0.12 |
rpoA | 3877949 | p.Thr187Ala | missense_variant | 1.0 |
embC | 4239677 | c.-186C>A | upstream_gene_variant | 0.11 |
embC | 4239951 | p.Arg30Leu | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243346 | c.114A>G | synonymous_variant | 0.87 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244058 | c.827delA | frameshift_variant | 0.12 |
embA | 4244748 | p.Thr506Ala | missense_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268218 | p.Trp207Arg | missense_variant | 0.17 |
ubiA | 4269298 | p.Ile179Thr | missense_variant | 1.0 |
ubiA | 4269323 | p.Pro171Ser | missense_variant | 0.12 |
ethA | 4328271 | c.-798A>G | upstream_gene_variant | 0.12 |
ethA | 4328416 | c.-943G>T | upstream_gene_variant | 0.12 |
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 |