TB-Profiler result

Run: ERR046766
Summary

Run ID: ERR046766

Sample name:

Date: 31-03-2023 08:50:12

Number of reads: 8137586

Percentage reads mapped: 99.66

Strain: lineage4.8.2

Drug-resistance: Sensitive

Download CSV Download TXT Download PDF Download JSON
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
lineage4.8.2 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
gyrB 5347 c.108G>C synonymous_variant 0.15
gyrA 7362 p.Glu21Gln missense_variant 1.0
gyrA 8135 c.834C>T synonymous_variant 1.0
mshA 576751 p.Lys468Asn missense_variant 0.21
rpoB 759620 c.-187A>C upstream_gene_variant 0.32
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 776891 p.Gln530His missense_variant 1.0
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 1475363 n.1706C>A non_coding_transcript_exon_variant 0.2
inhA 1674892 p.Asn231Asp missense_variant 0.2
tlyA 1917972 c.33A>G synonymous_variant 1.0
PPE35 2167871 c.2742G>C synonymous_variant 0.23
PPE35 2168149 p.Pro822Ser missense_variant 1.0
PPE35 2169866 c.747G>C synonymous_variant 0.36
PPE35 2170156 p.Ala153Pro missense_variant 0.28
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
eis 2714366 p.Val323Leu missense_variant 0.19
eis 2715586 c.-254G>C upstream_gene_variant 0.24
Rv2752c 3064552 p.Arg547Pro missense_variant 0.18
Rv2752c 3064741 p.Gly484Ala missense_variant 0.21
Rv3083 3448497 c.-7T>A upstream_gene_variant 1.0
fbiB 3641955 p.Gly141Arg missense_variant 0.19
alr 3840268 p.Thr385Pro missense_variant 0.25
clpC1 4038857 c.1848C>A synonymous_variant 0.14
clpC1 4039729 p.Asp326Asn missense_variant 1.0
clpC1 4039932 p.Gly258Val missense_variant 0.31
embC 4241456 p.Ala532Pro missense_variant 0.31
embC 4242476 p.Pro872Ala missense_variant 0.19
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embC 4242822 p.Val987Gly missense_variant 0.34
embC 4242827 p.Leu989Val missense_variant 0.19
embA 4244375 c.1143C>G synonymous_variant 0.17
embA 4246423 p.Val1064Gly missense_variant 0.23
ubiA 4269529 p.Ala102Gly missense_variant 0.14
ethA 4327672 c.-199G>A upstream_gene_variant 0.23
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
Rv3083 3448476 c.-27_*1408del transcript_ablation 1.0