TB-Profiler result

Run: ERR046732
Summary

Run ID: ERR046732

Sample name:

Date: 31-03-2023 08:48:17

Number of reads: 7688803

Percentage reads mapped: 99.31

Strain: lineage4.3.4.2.1

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
lineage4 Euro-American LAM;T;S;X;H None 1.0
lineage4.3 Euro-American (LAM) mainly-LAM None 1.0
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
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 0.99
gyrA 7362 p.Glu21Gln missense_variant 1.0
gyrA 7585 p.Ser95Thr missense_variant 1.0
gyrA 9304 p.Gly668Asp missense_variant 1.0
mshA 576751 p.Lys468Asn missense_variant 0.21
rpoC 762836 c.-534C>G upstream_gene_variant 0.37
rpoC 764725 p.Phe452Leu missense_variant 0.21
rpoC 764751 p.Val461Gly missense_variant 0.21
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
Rv1258c 1406750 c.591C>A synonymous_variant 0.21
atpE 1461019 c.-26C>A upstream_gene_variant 0.2
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rrl 1475363 n.1706C>A non_coding_transcript_exon_variant 0.26
inhA 1674892 p.Asn231Asp missense_variant 0.26
tlyA 1917972 c.33A>G synonymous_variant 1.0
PPE35 2169866 c.747G>C synonymous_variant 0.31
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
eis 2714366 p.Val323Leu missense_variant 0.39
pepQ 2859381 c.1038C>G synonymous_variant 0.19
Rv2752c 3064741 p.Gly484Ala missense_variant 0.24
Rv2752c 3065265 c.927C>G synonymous_variant 0.23
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
fprA 3475280 p.Val425Gly missense_variant 0.3
Rv3236c 3612009 p.Ala370Thr missense_variant 1.0
fbiB 3641955 p.Gly141Arg missense_variant 0.23
fbiB 3642772 p.Asp413Ala missense_variant 0.18
alr 3840719 c.702A>G synonymous_variant 1.0
rpoA 3878238 p.Asp90Glu missense_variant 0.15
rpoA 3878641 c.-135delG upstream_gene_variant 0.11
ddn 3987013 p.Gly57Ala missense_variant 0.23
clpC1 4038287 c.2418C>T synonymous_variant 0.99
clpC1 4039932 p.Gly258Val missense_variant 0.41
embC 4241456 p.Ala532Pro missense_variant 0.42
embC 4242476 p.Pro872Ala missense_variant 0.21
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embC 4242822 p.Val987Gly missense_variant 0.22
embA 4246423 p.Val1064Gly missense_variant 0.26
ubiA 4269529 p.Ala102Gly missense_variant 0.21
ethA 4327672 c.-199G>A upstream_gene_variant 0.33
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
gid 4408156 p.Leu16Arg missense_variant 1.0