TB-Profiler result

Run: SRR1172365
Summary

Run ID: SRR1172365

Sample name:

Date: 03-04-2023 03:05:06

Number of reads: 995136

Percentage reads mapped: 98.11

Strain: lineage4.4.1.1.1;lineage4.3.4.2.1

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
lineage4 Euro-American LAM;T;S;X;H None 1.0
lineage4.3 Euro-American (LAM) mainly-LAM None 0.5
lineage4.4 Euro-American S;T None 0.49
lineage4.4.1 Euro-American (S-type) S;T None 0.51
lineage4.3.4 Euro-American (LAM) LAM RD174 0.52
lineage4.4.1.1 Euro-American S;Orphans None 0.56
lineage4.4.1.1.1 Euro-American S;Orphans None 0.52
lineage4.3.4.2.1 Euro-American (LAM) LAM11 RD174 0.57
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 761140 p.His445Leu missense_variant 0.56 rifampicin
rpoB 761155 p.Ser450Leu missense_variant 0.47 rifampicin
rpsL 781687 p.Lys43Arg missense_variant 0.46 streptomycin
rrs 1473246 n.1401A>G non_coding_transcript_exon_variant 0.31 kanamycin, capreomycin, aminoglycosides, amikacin
katG 2155168 p.Ser315Thr missense_variant 1.0 isoniazid
pncA 2289142 p.Tyr34Asp missense_variant 0.5 pyrazinamide
embB 4247431 p.Met306Ile missense_variant 0.55 ethambutol
embB 4247730 p.Gly406Ala missense_variant 0.5 ethambutol
embB 4249583 p.Asp1024Asn missense_variant 0.58 ethambutol
ethA 4326974 c.487_499delCATCCGCAGCACT frameshift_variant 0.1 ethionamide
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 6140 p.Val301Leu missense_variant 0.64
gyrA 7362 p.Glu21Gln missense_variant 1.0
gyrA 7585 p.Ser95Thr missense_variant 1.0
gyrA 9304 p.Gly668Asp missense_variant 1.0
mshA 575538 p.Asp64Gly missense_variant 0.57
rpoC 764744 p.Arg459Trp missense_variant 0.52
rpoC 764995 c.1626C>G synonymous_variant 0.57
rpoC 765494 p.Val709Leu missense_variant 0.59
rpoC 766487 p.Pro1040Ser missense_variant 0.45
mmpL5 775639 p.Ile948Val missense_variant 1.0
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
fbiC 1302896 c.-35C>A upstream_gene_variant 0.13
fbiC 1303132 p.Ala68Ser missense_variant 0.12
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
tlyA 1917972 c.33A>G synonymous_variant 1.0
ndh 2102990 p.Val18Ala missense_variant 0.41
PPE35 2168320 p.Thr765Pro missense_variant 0.11
PPE35 2169840 p.Gly258Asp missense_variant 0.43
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
folC 2746645 p.Gln318His missense_variant 0.11
ribD 2986827 c.-12G>A upstream_gene_variant 0.38
Rv2752c 3064993 p.Trp400* stop_gained 0.64
thyA 3073868 p.Thr202Ala missense_variant 0.68
ald 3086788 c.-32T>C upstream_gene_variant 1.0
fbiD 3339287 p.Arg57Leu missense_variant 0.53
Rv3083 3448608 c.105G>A synonymous_variant 0.55
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
Rv3236c 3612009 p.Ala370Thr missense_variant 0.64
Rv3236c 3612665 p.Val151Ala missense_variant 0.48
alr 3840719 c.702A>G synonymous_variant 0.74
clpC1 4038287 c.2418C>T synonymous_variant 0.45
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embA 4244015 p.Leu261Phe missense_variant 0.14
ubiA 4269308 p.Phe176Leu missense_variant 0.38
ethA 4326853 c.612_620dupGCTGCAGCG disruptive_inframe_insertion 0.37
whiB6 4338235 p.Arg96Leu missense_variant 0.11
whiB6 4338312 c.210G>C synonymous_variant 0.12
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
gid 4407714 p.Lys163Asn missense_variant 0.43
gid 4407945 c.258C>A synonymous_variant 0.11
gid 4408156 p.Leu16Arg missense_variant 0.52