TB-Profiler result

Run: SRR10868988
Summary

Run ID: SRR10868988

Sample name:

Date: 02-04-2023 19:34:53

Number of reads: 1334085

Percentage reads mapped: 99.53

Strain: lineage4.1.2.1;lineage2.2.1.1

Drug-resistance: Sensitive

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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 0.39
lineage4 Euro-American LAM;T;S;X;H None 0.64
lineage4.1 Euro-American T;X;H None 0.57
lineage2.2 East-Asian (Beijing) Beijing-RD207 RD105;RD207 0.35
lineage4.1.2 Euro-American T;H None 0.64
lineage2.2.1 East-Asian (Beijing) Beijing-RD181 RD105;RD207;RD181 0.36
lineage4.1.2.1 Euro-American (Haarlem) T1;H1 RD182 0.64
lineage2.2.1.1 East-Asian (Beijing) Beijing-RD150 RD105;RD207;RD181;RD150 0.31
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
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 1.0
fgd1 491591 p.Lys270Met missense_variant 0.57
fgd1 491742 c.960T>C synonymous_variant 0.25
mshA 575679 p.Asn111Ser missense_variant 0.47
mshA 575907 p.Ala187Val missense_variant 0.25
mshA 576108 p.Ala254Gly missense_variant 0.26
ccsA 620625 p.Ile245Met missense_variant 0.31
rpoB 760115 c.309C>T synonymous_variant 0.76
rpoC 763031 c.-339T>C upstream_gene_variant 0.43
rpoC 765150 p.Gly594Glu missense_variant 0.63
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 776100 p.Thr794Ile missense_variant 0.39
mmpL5 776182 p.Asp767Asn missense_variant 0.45
mmpS5 779615 c.-710C>G upstream_gene_variant 0.33
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
fbiC 1302818 c.-113G>C upstream_gene_variant 0.45
Rv1258c 1406760 c.580_581insC frameshift_variant 0.35
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rpsA 1834177 c.636A>C synonymous_variant 0.39
tlyA 1917972 c.33A>G synonymous_variant 1.0
katG 2154724 p.Arg463Leu missense_variant 0.44
PPE35 2167926 p.Leu896Ser missense_variant 0.4
Rv1979c 2223014 p.Tyr51Asn missense_variant 0.35
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
kasA 2518076 c.-39C>T upstream_gene_variant 0.57
eis 2714846 p.Val163Ile missense_variant 0.31
eis 2715436 c.-104G>A upstream_gene_variant 0.62
ald 3086788 c.-32T>C upstream_gene_variant 1.0
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
fprA 3474930 c.924C>T synonymous_variant 0.33
Rv3236c 3612813 p.Thr102Ala missense_variant 0.41
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embC 4242803 p.Val981Leu missense_variant 0.66
embA 4243460 c.228C>T synonymous_variant 0.32
embB 4248115 c.1602C>T synonymous_variant 0.47
aftB 4267647 p.Asp397Gly missense_variant 0.47
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
gid 4407588 c.615A>G synonymous_variant 0.31
gid 4407927 p.Glu92Asp missense_variant 0.21