TB-Profiler result

Run: ERR216947

Summary

Run ID: ERR216947

Sample name:

Date: 31-03-2023 15:56:38

Number of reads: 1231622

Percentage reads mapped: 97.56

Strain: lineage4.3.4.2.1

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
lineage4 Euro-American LAM;T;S;X;H None 1.0
lineage4.3 Euro-American (LAM) mainly-LAM None 0.99
lineage4.3.4 Euro-American (LAM) LAM RD174 1.0
lineage4.3.4.2 Euro-American (LAM) LAM1;LAM4;LAM11 RD174 1.0
lineage4.3.4.2.1 Euro-American (LAM) LAM11 RD174 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
panD 4043906 p.Glu126* stop_gained 0.12 pyrazinamide
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 6140 p.Val301Leu missense_variant 1.0
gyrA 7362 p.Glu21Gln missense_variant 1.0
gyrA 7585 p.Ser95Thr missense_variant 1.0
gyrA 9304 p.Gly668Asp missense_variant 1.0
rpoB 761920 p.Gly705Asp missense_variant 0.12
rpoB 762587 p.Glu927Asp missense_variant 0.15
rpoC 764179 c.810C>T synonymous_variant 0.12
rpoC 764995 c.1626C>G synonymous_variant 1.0
mmpL5 775639 p.Ile948Val missense_variant 1.0
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
fbiC 1303906 p.Gly326Ser missense_variant 0.17
fbiC 1304825 p.Ala632Val missense_variant 0.12
Rv1258c 1406149 p.Pro398Ser missense_variant 0.11
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rrl 1475098 n.1441G>A non_coding_transcript_exon_variant 0.22
rrl 1476522 n.2865G>T non_coding_transcript_exon_variant 0.14
inhA 1674952 p.Pro251Ala missense_variant 0.17
tlyA 1917972 c.33A>G synonymous_variant 1.0
katG 2153933 p.Ala727Ser missense_variant 0.29
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
pncA 2289562 c.-321G>A upstream_gene_variant 0.14
eis 2714324 p.Arg337Ser missense_variant 0.12
folC 2747263 c.336C>A synonymous_variant 0.18
Rv2752c 3064840 p.Gly451Asp missense_variant 0.11
thyA 3073868 p.Thr202Ala missense_variant 1.0
ald 3086788 c.-32T>C upstream_gene_variant 1.0
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
Rv3236c 3612009 p.Ala370Thr missense_variant 1.0
alr 3840719 c.702A>G synonymous_variant 1.0
clpC1 4038287 c.2418C>T synonymous_variant 1.0
clpC1 4038882 p.Gly608Val missense_variant 0.2
embC 4240609 c.747C>T synonymous_variant 0.13
embC 4242425 p.Arg855Gly missense_variant 0.27
embA 4242643 c.-590C>T upstream_gene_variant 1.0
ethR 4328041 p.Thr165Ala missense_variant 0.18
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
gid 4408156 p.Leu16Arg missense_variant 1.0