TB-Profiler result

Run: SRR25827495

Summary

Run ID: SRR25827495

Sample name:

Date: 02-02-2024 06:25:16

Number of reads: 9836081

Percentage reads mapped: 98.44

Strain: lineage2.2.1;lineage1.1.2

Drug-resistance: MDR-TB


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Drug resistance: This table reports drug-resistance associated mutations found in known resistance genes
Drug Resistance Supporting mutations
Rifampicin R rpoB p.Ser450Leu (0.47)
Isoniazid R katG p.Ser315Thr (0.29)
Ethambutol R embA c.-12C>T (0.36), embB p.Gln853Pro (0.34)
Pyrazinamide
Streptomycin R rpsL p.Lys43Arg (0.42)
Fluoroquinolones
Moxifloxacin
Ofloxacin
Levofloxacin
Ciprofloxacin
Aminoglycosides
Amikacin
Capreomycin
Kanamycin
Cycloserine
Ethionamide
Clofazimine
Para-aminosalicylic_acid R thyX c.-16C>T (0.41)
Delamanid
Bedaquiline
Linezolid
Lineage Table: The lineage is inferred by analysing lineage specific SNPs
Lineage Family Main Spoligotype RDs Frequency
lineage2 East-Asian Beijing RD105 0.36
lineage1 Indo-Oceanic EAI RD239 0.65
lineage1.1 Indo-Oceanic EAI3;EAI4;EAI5;EAI6 RD239 0.65
lineage2.2 East-Asian (Beijing) Beijing-RD207 RD105;RD207 0.36
lineage1.1.2 Indo-Oceanic EAI3;EAI5 RD239 0.65
lineage2.2.1 East-Asian (Beijing) Beijing-RD181 RD105;RD207;RD181 0.34
Drug resistance-Associated Mutations: This table reports mutations found in candidate resistance genes which have been associated with drug resistance
Gene Chromosome position Mutation Type Estimated fraction Drugs
rpoB 761155 p.Ser450Leu missense_variant 0.47 rifampicin
rpsL 781687 p.Lys43Arg missense_variant 0.42 streptomycin
katG 2155168 p.Ser315Thr missense_variant 0.29 isoniazid
thyX 3067961 c.-16C>T upstream_gene_variant 0.41 para-aminosalicylic_acid
embA 4243221 c.-12C>T upstream_gene_variant 0.36 ethambutol
embB 4249071 p.Gln853Pro missense_variant 0.34 ethambutol
Non-Associated Mutations: This table reports mutations found in candidate resistance genes which have not been associated with drug resistance
Gene Chromosome position Mutation Type Estimated fraction
gyrB 6112 p.Met291Ile missense_variant 0.6
gyrB 6124 c.885C>T synonymous_variant 0.6
gyrA 7283 c.-19G>T upstream_gene_variant 0.33
gyrA 7362 p.Glu21Gln missense_variant 1.0
gyrA 7585 p.Ser95Thr missense_variant 1.0
gyrA 8452 p.Ala384Val missense_variant 0.63
gyrA 9143 c.1842T>C synonymous_variant 0.62
gyrA 9304 p.Gly668Asp missense_variant 1.0
fgd1 491742 c.960T>C synonymous_variant 1.0
mshA 575907 p.Ala187Val missense_variant 0.33
ccsA 620625 p.Ile245Met missense_variant 0.4
rpoB 760490 c.684C>T synonymous_variant 0.64
rpoC 763031 c.-339T>C upstream_gene_variant 1.0
rpoC 763884 p.Ala172Val missense_variant 0.64
rpoC 763886 c.517C>A synonymous_variant 0.63
rpoC 765171 p.Pro601Leu missense_variant 0.6
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 776100 p.Thr794Ile missense_variant 1.0
mmpL5 776182 p.Asp767Asn missense_variant 0.37
mmpL5 776395 p.Phe696Leu missense_variant 0.71
mmpS5 779615 c.-710C>G upstream_gene_variant 0.32
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
Rv1258c 1406760 c.580_581insC frameshift_variant 0.37
embR 1417019 p.Cys110Tyr missense_variant 0.57
embR 1417469 c.-122C>T upstream_gene_variant 0.64
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rpsA 1834177 c.636A>C synonymous_variant 0.41
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
PPE35 2167983 p.Gly877Asp missense_variant 0.64
Rv1979c 2222308 p.Asp286Gly missense_variant 0.69
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
kasA 2518132 c.18C>T synonymous_variant 0.67
ahpC 2726051 c.-142G>A upstream_gene_variant 0.62
Rv2752c 3064632 c.1560C>T synonymous_variant 0.59
thyA 3074069 p.Val135Phe missense_variant 0.35
ald 3086788 c.-32T>C upstream_gene_variant 1.0
ald 3087749 c.930C>T synonymous_variant 0.65
Rv3083 3448714 p.Asp71His missense_variant 0.64
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
fprA 3474597 c.591C>A synonymous_variant 0.69
fprA 3475159 p.Asn385Asp missense_variant 0.6
whiB7 3568739 c.-60C>A upstream_gene_variant 0.67
Rv3236c 3612813 p.Thr102Ala missense_variant 0.34
clpC1 4040517 p.Val63Ala missense_variant 0.65
embC 4240671 p.Thr270Ile missense_variant 0.63
embC 4241042 p.Asn394Asp missense_variant 0.65
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embA 4243460 c.228C>T synonymous_variant 0.36
embA 4243848 p.Val206Met missense_variant 0.66
embA 4244167 p.Ala312Val missense_variant 0.64
embA 4245835 p.Leu868Arg missense_variant 0.16
embA 4245969 p.Pro913Ser missense_variant 0.6
embB 4247646 p.Glu378Ala missense_variant 0.58
embB 4249757 p.Thr1082Ala missense_variant 0.33
aftB 4267647 p.Asp397Gly missense_variant 0.27
ubiA 4269387 p.Glu149Asp missense_variant 0.61
aftB 4269606 c.-770T>C upstream_gene_variant 0.67
ethA 4326432 p.Leu348Phe missense_variant 0.68
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
whiB6 4338603 c.-82C>T upstream_gene_variant 0.66
gid 4407588 c.615A>G synonymous_variant 1.0
gid 4407873 c.330G>T synonymous_variant 0.62
gid 4407927 p.Glu92Asp missense_variant 0.39