TB-Profiler result

Run: ERR067738
Summary

Run ID: ERR067738

Sample name:

Date: 31-03-2023 09:08:01

Number of reads: 4398662

Percentage reads mapped: 99.58

Strain: lineage4.3.3;lineage2.2.1

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
Lineage Table: The lineage is inferred by analysing lineage specific SNPs
Lineage Family Main Spoligotype RDs Frequency
lineage2 East-Asian Beijing RD105 0.69
lineage4 Euro-American LAM;T;S;X;H None 0.3
lineage4.3 Euro-American (LAM) mainly-LAM None 0.27
lineage2.2 East-Asian (Beijing) Beijing-RD207 RD105;RD207 0.74
lineage2.2.1 East-Asian (Beijing) Beijing-RD181 RD105;RD207;RD181 0.71
lineage4.3.3 Euro-American (LAM) LAM;T RD115 0.26
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 761139 p.His445Asp missense_variant 0.25 rifampicin
rpoB 761155 p.Ser450Leu missense_variant 0.69 rifampicin
rpsL 781687 p.Lys43Arg missense_variant 0.71 streptomycin
rrs 1472359 n.514A>C non_coding_transcript_exon_variant 0.26 streptomycin
fabG1 1673425 c.-15C>T upstream_gene_variant 0.3 isoniazid, ethionamide
katG 2155168 p.Ser315Thr missense_variant 1.0 isoniazid
eis 2715342 c.-10G>A upstream_gene_variant 0.65 kanamycin
folC 2747151 p.Ser150Gly missense_variant 0.73 para-aminosalicylic_acid
embA 4243217 c.-16C>T upstream_gene_variant 0.72 ethambutol
embB 4247729 p.Gly406Cys missense_variant 0.3 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 8040 p.Gly247Ser missense_variant 0.29
gyrA 9304 p.Gly668Asp missense_variant 1.0
fgd1 491742 c.960T>C synonymous_variant 0.64
mshA 575907 p.Ala187Val missense_variant 0.68
ccsA 620625 p.Ile245Met missense_variant 0.67
rpoC 763031 c.-339T>C upstream_gene_variant 0.8
rpoC 764817 p.Val483Gly missense_variant 0.71
rpoC 764995 c.1626C>G synonymous_variant 0.29
rpoC 766645 p.Glu1092Asp missense_variant 0.71
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 776100 p.Thr794Ile missense_variant 0.69
mmpL5 776182 p.Asp767Asn missense_variant 0.67
mmpS5 779615 c.-710C>G upstream_gene_variant 0.77
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
fbiC 1303095 c.165G>A synonymous_variant 0.42
fbiC 1304962 p.Trp678Gly missense_variant 0.3
Rv1258c 1406760 c.580_581insC frameshift_variant 0.61
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rpsA 1834177 c.636A>C synonymous_variant 0.74
rpsA 1834836 p.Met432Thr missense_variant 0.27
tlyA 1917972 c.33A>G synonymous_variant 1.0
katG 2154724 p.Arg463Leu missense_variant 0.74
katG 2156196 c.-85C>T upstream_gene_variant 0.31
PPE35 2167926 p.Leu896Ser missense_variant 0.73
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
kasA 2518919 p.Gly269Ser missense_variant 0.27
folC 2746340 p.Ala420Val missense_variant 0.3
ribD 2986827 c.-12G>A upstream_gene_variant 0.24
ribD 2987307 p.Ala157Pro missense_variant 0.27
thyA 3073806 c.666C>G synonymous_variant 0.2
thyA 3073868 p.Thr202Ala missense_variant 0.29
ald 3086788 c.-32T>C upstream_gene_variant 1.0
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
Rv3236c 3612813 p.Thr102Ala missense_variant 0.72
rpoA 3877981 p.Tyr176Cys missense_variant 0.14
clpC1 4038287 c.2418C>T synonymous_variant 0.35
clpC1 4038857 c.1848C>A synonymous_variant 0.2
clpC1 4038968 c.1737G>A synonymous_variant 0.25
embC 4239842 c.-21C>A upstream_gene_variant 0.24
embA 4242643 c.-590C>T upstream_gene_variant 0.99
embA 4243460 c.228C>T synonymous_variant 0.68
aftB 4267647 p.Asp397Gly missense_variant 0.73
ethA 4326761 p.Val238Gly missense_variant 0.71
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
gid 4407588 c.615A>G synonymous_variant 0.7
gid 4407927 p.Glu92Asp missense_variant 0.82
gid 4408156 p.Leu16Arg missense_variant 0.29