TB-Profiler result

Run: SRR1169026
Summary

Run ID: SRR1169026

Sample name:

Date: 03-04-2023 02:38:29

Number of reads: 3312779

Percentage reads mapped: 99.6

Strain: lineage4.3.3;lineage2.2.1

Drug-resistance: Other

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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 0.43
lineage4 Euro-American LAM;T;S;X;H None 0.6
lineage4.3 Euro-American (LAM) mainly-LAM None 0.55
lineage2.2 East-Asian (Beijing) Beijing-RD207 RD105;RD207 0.47
lineage2.2.1 East-Asian (Beijing) Beijing-RD181 RD105;RD207;RD181 0.42
lineage4.3.3 Euro-American (LAM) LAM;T RD115 0.54
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
gid 4408087 c.115delC frameshift_variant 0.44 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 0.49
gyrA 9304 p.Gly668Asp missense_variant 1.0
fgd1 491742 c.960T>C synonymous_variant 0.4
mshA 575907 p.Ala187Val missense_variant 0.33
ccsA 620625 p.Ile245Met missense_variant 0.49
rpoC 763031 c.-339T>C upstream_gene_variant 0.52
rpoC 764995 c.1626C>G synonymous_variant 0.67
rpoC 766645 p.Glu1092Asp missense_variant 0.42
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 776100 p.Thr794Ile missense_variant 0.39
mmpL5 776182 p.Asp767Asn missense_variant 0.47
mmpS5 779615 c.-710C>G upstream_gene_variant 0.48
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
fbiC 1303095 c.165G>A synonymous_variant 0.49
Rv1258c 1406089 p.Ala418Ser missense_variant 0.47
Rv1258c 1406760 c.580_581insC frameshift_variant 0.33
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rpsA 1834177 c.636A>C synonymous_variant 0.56
rpsA 1834836 p.Met432Thr missense_variant 0.44
tlyA 1917972 c.33A>G synonymous_variant 1.0
katG 2154724 p.Arg463Leu missense_variant 0.49
katG 2156196 c.-85C>T upstream_gene_variant 0.55
PPE35 2167926 p.Leu896Ser missense_variant 0.36
Rv1979c 2222112 c.1052dupT frameshift_variant 0.54
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
pncA 2290080 c.-839T>A upstream_gene_variant 0.53
kasA 2518919 p.Gly269Ser missense_variant 0.65
folC 2746340 p.Ala420Val missense_variant 0.42
Rv2752c 3066133 p.Ala20Val missense_variant 0.52
thyA 3073868 p.Thr202Ala missense_variant 0.52
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 0.51
clpC1 4038287 c.2418C>T synonymous_variant 0.41
clpC1 4038968 c.1737G>A synonymous_variant 0.52
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embA 4243460 c.228C>T synonymous_variant 0.39
aftB 4267647 p.Asp397Gly missense_variant 0.52
ethA 4327406 p.Leu23Arg missense_variant 0.34
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
gid 4407588 c.615A>G synonymous_variant 0.27
gid 4407797 p.Ser136Pro missense_variant 0.49
gid 4407927 p.Glu92Asp missense_variant 0.45
gid 4408156 p.Leu16Arg missense_variant 0.62