Run ID: SRR25827744
Sample name:
Date: 02-02-2024 18:05:17
Number of reads: 9830290
Percentage reads mapped: 98.83
Strain: lineage2.2.1;lineage1.1.3.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | R | rpoB p.Ser450Leu (0.48), rpoC p.Ile491Thr (0.35) |
Isoniazid | R | fabG1 c.-17G>T (0.40), katG p.Ser315Thr (0.40) |
Ethambutol | R | embA c.-16C>T (0.42) |
Pyrazinamide | R | pncA p.Ile5Ser (0.42) |
Streptomycin | R | rpsL p.Lys43Arg (0.40) |
Fluoroquinolones | R | gyrA p.Asp94Gly (0.36) |
Moxifloxacin | R | gyrA p.Asp94Gly (0.36) |
Ofloxacin | R | gyrA p.Asp94Gly (0.36) |
Levofloxacin | R | gyrA p.Asp94Gly (0.36) |
Ciprofloxacin | R | gyrA p.Asp94Gly (0.36) |
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | R | eis c.-12C>T (0.39) |
Cycloserine | ||
Ethionamide | R | fabG1 c.-17G>T (0.40), ethA c.1203delT (0.38) |
Clofazimine | ||
Para-aminosalicylic_acid | R | thyA p.Thr22Ala (0.42) |
Delamanid | ||
Bedaquiline | ||
Linezolid |
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.41 |
lineage1 | Indo-Oceanic | EAI | RD239 | 0.56 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.58 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.42 |
lineage1.1.3 | Indo-Oceanic | EAI6 | RD239 | 0.55 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.4 |
lineage1.1.3.1 | Indo-Oceanic | NA | RD239 | 0.56 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.36 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.48 | rifampicin |
rpoC | 764841 | p.Ile491Thr | missense_variant | 0.35 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.4 | streptomycin |
fabG1 | 1673423 | c.-17G>T | upstream_gene_variant | 0.4 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.4 | isoniazid |
pncA | 2289228 | p.Ile5Ser | missense_variant | 0.42 | pyrazinamide |
eis | 2715344 | c.-12C>T | upstream_gene_variant | 0.39 | kanamycin |
thyA | 3074408 | p.Thr22Ala | missense_variant | 0.42 | para-aminosalicylic_acid |
embA | 4243217 | c.-16C>T | upstream_gene_variant | 0.42 | ethambutol |
ethA | 4326270 | c.1203delT | frameshift_variant | 0.38 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.59 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.55 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.53 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491290 | p.Val170Met | missense_variant | 0.53 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.98 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.42 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.43 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.97 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.54 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.54 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 0.63 |
rpoC | 765230 | p.Ala621Thr | missense_variant | 0.6 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.99 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.42 |
mmpS5 | 779526 | c.-621G>A | upstream_gene_variant | 0.59 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.44 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.43 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.48 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.42 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918254 | c.315C>T | synonymous_variant | 0.59 |
ndh | 2102380 | c.663G>T | synonymous_variant | 0.54 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.98 |
katG | 2155416 | c.696G>A | synonymous_variant | 0.54 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.56 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.57 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.56 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.57 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.54 |
thyX | 3067949 | c.-4C>T | upstream_gene_variant | 0.48 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.56 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.58 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.55 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.4 |
alr | 3841253 | c.168C>T | synonymous_variant | 0.45 |
rpoA | 3878637 | c.-130G>C | upstream_gene_variant | 0.22 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.54 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.57 |
embC | 4241022 | p.Ala387Val | missense_variant | 0.43 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.58 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.43 |
embA | 4243848 | p.Val206Met | missense_variant | 0.53 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.58 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.54 |
embB | 4247847 | p.Gln445Arg | missense_variant | 0.32 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.33 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.61 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.55 |
ethA | 4327546 | c.-73T>A | upstream_gene_variant | 0.51 |
whiB6 | 4338292 | p.Ala77Val | missense_variant | 0.43 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.99 |
gid | 4407620 | p.Tyr195His | missense_variant | 0.4 |
gid | 4407780 | c.423G>A | synonymous_variant | 0.54 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.57 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.38 |