Run ID: SRR3082103
Sample name:
Date: 04-04-2023 04:53:44
Number of reads: 582830
Percentage reads mapped: 98.75
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 | 7581 | p.Asp94Asn | 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 | 2288764 | p.Thr160Ala | missense_variant | 1.0 | pyrazinamide |
pncA | 2288781 | p.Arg154Met | missense_variant | 1.0 | pyrazinamide |
eis | 2715342 | c.-10G>A | upstream_gene_variant | 1.0 | kanamycin |
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 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 762226 | p.Glu807Gly | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763699 | c.330G>A | synonymous_variant | 0.12 |
rpoC | 764673 | p.Gln435Arg | missense_variant | 0.18 |
rpoC | 764723 | p.Phe452Leu | missense_variant | 1.0 |
rpoC | 767198 | p.Glu1277Gln | missense_variant | 0.12 |
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 |
fbiC | 1303144 | p.Ser72Pro | missense_variant | 0.15 |
fbiC | 1304684 | p.Ala585Val | missense_variant | 0.12 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473199 | n.1354C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476117 | n.2460G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476326 | n.2673delA | non_coding_transcript_exon_variant | 0.13 |
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 |
folC | 2746347 | p.Ala418Thr | missense_variant | 0.12 |
Rv2752c | 3064780 | p.Gly471Asp | missense_variant | 1.0 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.17 |
thyA | 3073860 | c.612C>G | synonymous_variant | 0.29 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.18 |
thyA | 3073866 | c.606C>G | synonymous_variant | 0.18 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.15 |
thyA | 3073890 | c.580_582delTTGinsCTA | synonymous_variant | 0.13 |
thyA | 3073898 | p.Ala192Ser | missense_variant | 0.12 |
thyA | 3074449 | p.Leu8Pro | missense_variant | 0.14 |
ald | 3086731 | c.-89A>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 |
clpC1 | 4039966 | p.Leu247Ile | missense_variant | 0.12 |
clpC1 | 4040042 | c.663C>A | synonymous_variant | 0.14 |
embC | 4240201 | c.339G>T | synonymous_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4249567 | p.Tyr1018* | stop_gained | 0.2 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
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 |