TB-Profiler result

Run: ERR4799128

Summary

Run ID: ERR4799128

Sample name:

Date: 20-10-2023 03:28:58

Number of reads: 4093654

Percentage reads mapped: 99.58

Strain: lineage3.1.2.1

Drug-resistance: Pre-XDR-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 (1.00)
Isoniazid R katG p.Gly279Asp (0.74), katG p.Trp107Arg (0.21)
Ethambutol R embB p.Met306Ile (0.15)
Pyrazinamide R pncA p.Thr142Ala (0.37), pncA p.Trp68Arg (0.18)
Streptomycin
Fluoroquinolones R gyrA p.Asp94Gly (0.21)
Moxifloxacin R gyrA p.Asp94Gly (0.21)
Ofloxacin R gyrA p.Asp94Gly (0.21)
Levofloxacin R gyrA p.Asp94Gly (0.21)
Ciprofloxacin R gyrA p.Asp94Gly (0.21)
Aminoglycosides
Amikacin
Capreomycin
Kanamycin
Cycloserine
Ethionamide
Clofazimine
Para-aminosalicylic_acid
Delamanid
Bedaquiline
Linezolid
Lineage Table: The lineage is inferred by analysing lineage specific SNPs
Lineage Family Main Spoligotype RDs Frequency
lineage3 East-African-Indian CAS RD750 0.99
lineage3.1 East-African-Indian Non-CAS1-Delhi RD750 0.98
lineage3.1.2 East-African-Indian CAS;CAS2 RD750 0.99
lineage3.1.2.1 East-African-Indian CAS2 RD750 0.98
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
gyrA 7582 p.Asp94Gly missense_variant 0.21 ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin
rpoB 761155 p.Ser450Leu missense_variant 1.0 rifampicin
katG 2155276 p.Gly279Asp missense_variant 0.74 isoniazid
katG 2155793 p.Trp107Arg missense_variant 0.21 isoniazid
pncA 2288818 p.Thr142Ala missense_variant 0.37 pyrazinamide
pncA 2289040 p.Trp68Arg missense_variant 0.18 pyrazinamide
embB 4247431 p.Met306Ile missense_variant 0.15 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
gyrA 7362 p.Glu21Gln missense_variant 1.0
gyrA 7585 p.Ser95Thr missense_variant 1.0
gyrA 9304 p.Gly668Asp missense_variant 0.99
fgd1 491742 c.960T>C synonymous_variant 1.0
rpoB 759746 c.-61C>T upstream_gene_variant 0.98
rpoC 762434 c.-936T>G upstream_gene_variant 0.97
rpoC 763031 c.-339T>C upstream_gene_variant 1.0
rpoC 764712 p.Ala448Val missense_variant 0.16
rpoC 764819 p.Trp484Gly missense_variant 0.14
rpoC 765860 p.Phe831Val missense_variant 0.15
rpoC 766487 p.Pro1040Ala missense_variant 0.33
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 776100 p.Thr794Ile missense_variant 1.0
mmpS5 778941 c.-36A>G upstream_gene_variant 0.97
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rrl 1475988 n.2331A>G non_coding_transcript_exon_variant 1.0
rpsA 1833677 p.Val46Met missense_variant 0.99
tlyA 1917972 c.33A>G synonymous_variant 1.0
katG 2154724 p.Arg463Leu missense_variant 0.99
PPE35 2167926 p.Leu896Ser missense_variant 1.0
PPE35 2168604 p.Pro670Leu missense_variant 0.97
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
pncA 2289047 c.195C>T synonymous_variant 1.0
pncA 2289365 c.-125delC upstream_gene_variant 0.98
ahpC 2726105 c.-88G>A upstream_gene_variant 0.97
ald 3086788 c.-32T>C upstream_gene_variant 1.0
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
embC 4242075 p.Arg738Gln missense_variant 0.97
embA 4242643 c.-590C>T upstream_gene_variant 0.99
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
whiB6 4338599 c.-78A>C upstream_gene_variant 0.99
gid 4407588 c.615A>G synonymous_variant 1.0