TB-Profiler result

Run: ERR4828577
Summary

Run ID: ERR4828577

Sample name:

Date: 01-04-2023 18:57:59

Number of reads: 1606847

Percentage reads mapped: 99.54

Strain: lineage4.4.2;lineage2.2.1

Drug-resistance: HR-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 0.72
lineage4 Euro-American LAM;T;S;X;H None 0.28
lineage2.2 East-Asian (Beijing) Beijing-RD207 RD105;RD207 0.7
lineage4.4 Euro-American S;T None 0.29
lineage2.2.1 East-Asian (Beijing) Beijing-RD181 RD105;RD207;RD181 0.73
lineage4.4.2 Euro-American T1;T2 None 0.27
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
rpsL 781687 p.Lys43Arg missense_variant 0.73 streptomycin
katG 2155163 p.Ile317Val missense_variant 0.78 isoniazid
katG 2155168 p.Ser315Asn missense_variant 0.76 isoniazid
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 5977 c.801C>A synonymous_variant 0.22
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 491742 c.960T>C synonymous_variant 0.69
mshA 575907 p.Ala187Val missense_variant 0.68
ccsA 620625 p.Ile245Met missense_variant 0.72
rpoC 763031 c.-339T>C upstream_gene_variant 0.67
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 776100 p.Thr794Ile missense_variant 0.74
mmpL5 776182 p.Asp767Asn missense_variant 0.74
mmpS5 779615 c.-710C>G upstream_gene_variant 0.71
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
Rv1258c 1406760 c.580_581insC frameshift_variant 0.82
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rpsA 1834177 c.636A>C synonymous_variant 0.65
tlyA 1917972 c.33A>G synonymous_variant 1.0
katG 2154724 p.Arg463Leu missense_variant 0.76
PPE35 2167926 p.Leu896Ser missense_variant 0.69
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
Rv2752c 3066099 p.Met31Ile missense_variant 0.28
ald 3086788 c.-32T>C upstream_gene_variant 1.0
fbiD 3338931 c.-187C>A upstream_gene_variant 0.7
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
fprA 3474676 p.Val224Met missense_variant 0.24
Rv3236c 3612813 p.Thr102Ala missense_variant 0.73
alr 3840571 p.Val284Leu missense_variant 0.71
rpoA 3878613 c.-113_-107delCAACCCA upstream_gene_variant 0.14
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embA 4243460 c.228C>T synonymous_variant 0.78
embA 4244278 p.Pro349Gln missense_variant 0.46
embB 4246508 c.-6G>A upstream_gene_variant 0.13
aftB 4267647 p.Asp397Gly missense_variant 0.79
aftB 4268928 c.-92C>T upstream_gene_variant 0.38
aftB 4269375 c.-539G>A upstream_gene_variant 0.33
ethA 4326468 p.Asp336His missense_variant 0.46
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
gid 4407588 c.615A>G synonymous_variant 0.76
gid 4407927 p.Glu92Asp missense_variant 0.7