Run ID: ERR4799883
Sample name:
Date: 01-04-2023 09:26:20
Number of reads: 3336817
Percentage reads mapped: 99.28
Strain: lineage1.2.2.2
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.97 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 0.98 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 0.43 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrA | 7572 | p.Ser91Pro | missense_variant | 0.27 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.12 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761139 | p.His445Asp | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 0.92 | isoniazid, ethionamide |
inhA | 1674481 | p.Ser94Ala | missense_variant | 0.98 | isoniazid, ethionamide |
pncA | 2289091 | p.His51Tyr | missense_variant | 0.94 | pyrazinamide |
eis | 2715344 | c.-12C>T | upstream_gene_variant | 0.97 | kanamycin |
embB | 4247730 | p.Gly406Asp | missense_variant | 0.94 | ethambutol |
gid | 4407816 | c.386delG | frameshift_variant | 0.96 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 0.92 |
gyrB | 6112 | p.Met291Ile | missense_variant | 0.97 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 0.96 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8164 | p.Ala288Asp | missense_variant | 0.18 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.99 |
gyrA | 8513 | c.1212C>A | synonymous_variant | 0.96 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.93 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.99 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.98 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.96 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.99 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.99 |
mmpL5 | 777431 | c.1047_1049delCGC | disruptive_inframe_deletion | 0.93 |
mmpS5 | 779625 | c.-720G>A | upstream_gene_variant | 0.95 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.94 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102240 | p.Arg268His | missense_variant | 0.96 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 0.95 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.97 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288724 | p.Glu173Gly | missense_variant | 0.94 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.99 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.94 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.96 |
clpC1 | 4040719 | c.-15A>G | upstream_gene_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.97 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.97 |
aftB | 4267960 | p.Val293Met | missense_variant | 0.97 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.95 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.92 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 0.98 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 0.98 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407848 | p.Ala119Thr | missense_variant | 0.96 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.93 |