TB-Profiler result

Run: ERR11050555
Summary

Run ID: ERR11050555

Sample name:

Date: 03-04-2023 10:28:27

Number of reads: 4761667

Percentage reads mapped: 99.68

Strain: lineage4.8

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
lineage4 Euro-American LAM;T;S;X;H None 1.0
lineage4.8 Euro-American (mainly T) T1;T2;T3;T5 RD219 1.0
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 9647 c.2346C>G synonymous_variant 0.19
mshA 576108 p.Ala254Gly missense_variant 0.3
mshA 576113 p.Arg256Gly missense_variant 0.3
mshA 576442 p.Cys365Trp missense_variant 0.24
mshA 576453 p.Val369Gly missense_variant 0.19
mshA 576456 p.Val370Gly missense_variant 0.21
mshA 576616 c.1269G>C synonymous_variant 0.18
rpoB 760975 p.Met390Thr missense_variant 1.0
rpoC 764367 p.Gly333Ala missense_variant 0.18
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 777883 p.Gly200Arg missense_variant 0.16
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rrl 1474001 n.344C>T non_coding_transcript_exon_variant 1.0
rrl 1475090 n.1433A>C non_coding_transcript_exon_variant 1.0
fabG1 1673553 p.Asp38Glu missense_variant 0.32
tlyA 1917972 c.33A>G synonymous_variant 1.0
PPE35 2168149 p.Pro822Ser missense_variant 1.0
PPE35 2170065 p.Ala183Gly missense_variant 0.23
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
kasA 2519071 p.Asp319Glu missense_variant 0.18
pepQ 2860159 p.Ala87Gly missense_variant 0.19
ald 3086767 c.-53A>C upstream_gene_variant 0.99
fbiD 3339734 p.Ala206Gly missense_variant 0.68
fbiD 3339744 c.627A>C synonymous_variant 0.33
fbiD 3339746 p.Ala210Gly missense_variant 0.33
fbiD 3339749 p.Val211Ala missense_variant 0.3
fbiD 3339751 p.Ala212Pro missense_variant 0.4
Rv3083 3448497 c.-7T>A upstream_gene_variant 1.0
Rv3083 3448500 c.-4A>G upstream_gene_variant 1.0
Rv3083 3448501 c.-3G>T upstream_gene_variant 1.0
whiB7 3568431 c.249C>G synonymous_variant 0.24
rpoA 3878641 c.-134C>G upstream_gene_variant 0.67
embC 4240409 p.Pro183Ala missense_variant 0.28
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embA 4244990 c.1758G>C synonymous_variant 1.0
embB 4246527 p.Ala5Gly missense_variant 0.36
embB 4247016 p.Ser168Trp missense_variant 0.2
embB 4248328 c.1815G>C synonymous_variant 0.22
aftB 4267715 c.1122G>A synonymous_variant 1.0
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
Rv3083 3448507 c.5_*1408del frameshift_variant&stop_lost&splice_region_variant 1.0