Run ID: SRR2100184
Sample name:
Date: 19-10-2023 15:36:37
Number of reads: 4697401
Percentage reads mapped: 99.38
Strain: lineage4.1.1.3;lineage1.1.2
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Asp435Tyr (0.26) |
Isoniazid | ||
Ethambutol | ||
Pyrazinamide | R | panD p.Ile49Val (0.84) |
Streptomycin | ||
Fluoroquinolones | ||
Moxifloxacin | ||
Ofloxacin | ||
Levofloxacin | ||
Ciprofloxacin | ||
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | ||
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.8 |
lineage4.1 | Euro-American | T;X;H | None | 0.25 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.76 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 0.78 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 0.22 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 0.19 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761109 | p.Asp435Tyr | missense_variant | 0.26 | rifampicin |
panD | 4044137 | p.Ile49Val | missense_variant | 0.84 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5770 | c.531C>T | synonymous_variant | 0.8 |
gyrB | 6112 | p.Met291Ile | missense_variant | 0.79 |
gyrB | 6124 | c.885C>T | synonymous_variant | 0.77 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.74 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.79 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.78 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.75 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.74 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.73 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.22 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 0.77 |
rpoC | 765190 | c.1821G>A | synonymous_variant | 0.76 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.82 |
mmpR5 | 779434 | p.Val149Ile | missense_variant | 0.75 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406503 | p.Val280Leu | missense_variant | 0.79 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.69 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.79 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.8 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.83 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.76 |
Rv1979c | 2223170 | c.-6G>A | upstream_gene_variant | 0.23 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.76 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.74 |
ribD | 2987151 | p.His105Tyr | missense_variant | 0.75 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.68 |
Rv2752c | 3065598 | c.594G>A | synonymous_variant | 0.66 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.73 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.71 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.78 |
rpoA | 3878569 | c.-63_-62insG | upstream_gene_variant | 0.82 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.72 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.82 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.74 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.18 |
embA | 4243848 | p.Val206Met | missense_variant | 0.74 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.85 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.76 |
embB | 4249408 | c.2895G>A | synonymous_variant | 0.25 |
aftB | 4267867 | p.Leu324Met | missense_variant | 0.77 |
aftB | 4268461 | p.Ile126Val | missense_variant | 0.8 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.76 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.78 |
aftB | 4269630 | c.-794G>A | upstream_gene_variant | 0.71 |
whiB6 | 4338596 | c.-76_-75delAGinsC | upstream_gene_variant | 0.73 |
whiB6 | 4338596 | c.-75delG | upstream_gene_variant | 0.27 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.75 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.8 |
gid | 4407798 | c.405G>T | synonymous_variant | 0.29 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.71 |