Run ID: SRR25827375
Sample name:
Date: 01-02-2024 05:18:30
Number of reads: 7948425
Percentage reads mapped: 98.32
Strain: lineage2.2.1;lineage1.2.2.2
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Ser450Leu (0.26) |
Isoniazid | R | katG p.Ser315Thr (0.30), ahpC p.Glu76Lys (0.61) |
Ethambutol | R | embB p.Met306Val (0.20), embB p.Gln853Pro (0.24) |
Pyrazinamide | R | pncA p.Asp63Ala (0.17) |
Streptomycin | R | rpsL p.Lys43Arg (0.20) |
Fluoroquinolones | R | gyrA p.Asp94Tyr (0.19) |
Moxifloxacin | R | gyrA p.Asp94Tyr (0.19) |
Ofloxacin | R | gyrA p.Asp94Tyr (0.19) |
Levofloxacin | R | gyrA p.Asp94Tyr (0.19) |
Ciprofloxacin | R | gyrA p.Asp94Tyr (0.19) |
Aminoglycosides | R | rrs n.1401A>G (0.15) |
Amikacin | R | rrs n.1401A>G (0.15) |
Capreomycin | R | rrs n.1401A>G (0.15) |
Kanamycin | R | rrs n.1401A>G (0.15) |
Cycloserine | ||
Ethionamide | ||
Clofazimine | ||
Para-aminosalicylic_acid | R | thyX c.-16C>T (0.33) |
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.21 |
lineage1 | Indo-Oceanic | EAI | RD239 | 0.8 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.21 |
lineage1.2.2 | Indo-Oceanic | EAI1 | RD239 | 0.68 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.19 |
lineage1.2.2.2 | Indo-Oceanic | NA | RD239 | 0.68 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7581 | p.Asp94Tyr | missense_variant | 0.19 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.26 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.2 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.15 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.3 | isoniazid |
pncA | 2289054 | p.Asp63Ala | missense_variant | 0.17 | pyrazinamide |
ahpC | 2726418 | p.Glu76Lys | missense_variant | 0.61 | isoniazid |
thyX | 3067961 | c.-16C>T | upstream_gene_variant | 0.33 | para-aminosalicylic_acid |
embB | 4247429 | p.Met306Val | missense_variant | 0.2 | ethambutol |
embB | 4249071 | p.Gln853Pro | missense_variant | 0.24 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5075 | c.-165C>T | upstream_gene_variant | 0.7 |
gyrB | 6112 | p.Met291Ile | missense_variant | 0.77 |
gyrA | 7268 | c.-34C>T | upstream_gene_variant | 0.71 |
gyrA | 7283 | c.-19G>T | upstream_gene_variant | 0.21 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.79 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.82 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.19 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.82 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.81 |
rpoC | 764666 | p.Gly433Ser | missense_variant | 0.16 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.17 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.22 |
mmpS5 | 779625 | c.-720G>A | upstream_gene_variant | 0.67 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.21 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.75 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102240 | p.Arg268His | missense_variant | 0.71 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168742 | p.Gly624Asp | missense_variant | 0.62 |
Rv1979c | 2222159 | c.1006C>T | synonymous_variant | 0.76 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.78 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.77 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.77 |
pepQ | 2860365 | c.54G>T | synonymous_variant | 0.22 |
thyA | 3074069 | p.Val135Phe | missense_variant | 0.16 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.75 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.8 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.83 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.24 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.75 |
clpC1 | 4040719 | c.-15A>G | upstream_gene_variant | 0.68 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.81 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.73 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243217 | c.-16C>A | upstream_gene_variant | 0.21 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.18 |
embA | 4245835 | p.Leu868Arg | missense_variant | 0.15 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.76 |
embB | 4247015 | p.Ser168Ala | missense_variant | 0.21 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.82 |
embB | 4249757 | p.Thr1082Ala | missense_variant | 0.22 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.17 |
aftB | 4267960 | p.Val293Met | missense_variant | 0.74 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.78 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.79 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 0.69 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 0.75 |
whiB6 | 4338203 | p.Arg107Cys | missense_variant | 0.86 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.8 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407848 | p.Ala119Thr | missense_variant | 0.69 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.83 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.17 |