TB-Profiler result

Run: ERR4800294

Summary

Run ID: ERR4800294

Sample name:

Date: 20-10-2023 04:15:51

Number of reads: 2770066

Percentage reads mapped: 99.7

Strain: lineage4.3.3

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.Thr427Pro (0.97), rpoB p.Ser450Trp (1.00)
Isoniazid R katG p.Ser315Thr (0.97)
Ethambutol R embB p.Met306Val (1.00)
Pyrazinamide R pncA p.Ser67Pro (0.99)
Streptomycin R gid p.Pro75Arg (0.96)
Fluoroquinolones R gyrA p.Asp94Gly (0.99)
Moxifloxacin R gyrA p.Asp94Gly (0.99)
Ofloxacin R gyrA p.Asp94Gly (0.99)
Levofloxacin R gyrA p.Asp94Gly (0.99)
Ciprofloxacin R gyrA p.Asp94Gly (0.99)
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
lineage4 Euro-American LAM;T;S;X;H None 1.0
lineage4.3 Euro-American (LAM) mainly-LAM None 0.98
lineage4.3.3 Euro-American (LAM) LAM;T RD115 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 0.99 ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin
rpoB 761085 p.Thr427Pro missense_variant 0.97 rifampicin
rpoB 761155 p.Ser450Trp missense_variant 1.0 rifampicin
katG 2155168 p.Ser315Thr missense_variant 0.97 isoniazid
pncA 2289043 p.Ser67Pro missense_variant 0.99 pyrazinamide
embB 4247429 p.Met306Val missense_variant 1.0 ethambutol
gid 4407979 p.Pro75Arg missense_variant 0.96 streptomycin
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 8040 p.Gly247Ser missense_variant 0.99
gyrA 9304 p.Gly668Asp missense_variant 1.0
gyrA 9407 c.2106C>T synonymous_variant 1.0
rpoC 764995 c.1626C>G synonymous_variant 0.99
mmpL5 775639 p.Ile948Val missense_variant 1.0
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
Rv1258c 1407363 c.-23C>T upstream_gene_variant 0.97
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rpsA 1834836 p.Met432Thr missense_variant 0.93
tlyA 1917972 c.33A>G synonymous_variant 1.0
katG 2156196 c.-85C>T upstream_gene_variant 0.97
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
kasA 2518919 p.Gly269Ser missense_variant 1.0
folC 2746340 p.Ala420Val missense_variant 1.0
thyX 3067954 c.-9G>A upstream_gene_variant 0.99
thyA 3073868 p.Thr202Ala missense_variant 0.98
thyA 3074096 p.Arg126Gly missense_variant 1.0
ald 3086788 c.-32T>C upstream_gene_variant 1.0
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
rpoA 3877954 p.Gln185Arg missense_variant 0.98
clpC1 4038287 c.2418C>T synonymous_variant 0.96
embA 4242643 c.-590C>T upstream_gene_variant 1.0
ethA 4327296 p.Tyr60Asp missense_variant 1.0
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
whiB6 4338599 c.-78A>G upstream_gene_variant 0.26
gid 4408156 p.Leu16Arg missense_variant 0.99