TB-Profiler result

Run: ERR046976
Summary

Run ID: ERR046976

Sample name:

Date: 31-03-2023 08:59:35

Number of reads: 5051800

Percentage reads mapped: 99.45

Strain: lineage4.1.1

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
lineage4.1 Euro-American T;X;H None 1.0
lineage4.1.1 Euro-American (X-type) X1;X2;X3 None 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 7585 p.Ser95Thr missense_variant 1.0
gyrA 8626 p.Arg442His missense_variant 1.0
gyrA 9304 p.Gly668Asp missense_variant 1.0
mshA 576751 p.Lys468Asn missense_variant 0.22
ccsA 620748 c.858T>G synonymous_variant 0.22
rpoC 762836 c.-534C>G upstream_gene_variant 0.22
rpoC 765150 p.Gly594Glu missense_variant 1.0
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 777399 p.Thr361Arg missense_variant 0.18
mmpR5 779371 p.Ala128Pro missense_variant 0.31
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rrs 1473102 n.1257C>T non_coding_transcript_exon_variant 1.0
rrs 1473369 n.1524A>G non_coding_transcript_exon_variant 0.16
rrl 1475363 n.1706C>A non_coding_transcript_exon_variant 0.2
inhA 1674892 p.Asn231Asp missense_variant 0.33
tlyA 1917972 c.33A>G synonymous_variant 1.0
PPE35 2169866 c.747G>C synonymous_variant 0.42
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
eis 2714366 p.Val323Leu missense_variant 0.24
pepQ 2859381 c.1038C>G synonymous_variant 0.24
Rv2752c 3064552 p.Arg547Pro missense_variant 0.23
Rv2752c 3064741 p.Gly484Ala missense_variant 0.28
thyX 3067995 c.-50A>C upstream_gene_variant 0.22
ald 3086750 c.-70A>C upstream_gene_variant 1.0
ald 3086788 c.-32T>C upstream_gene_variant 1.0
fbiD 3339550 p.Gly145Trp missense_variant 0.23
fprA 3473996 c.-11_-10insA upstream_gene_variant 0.99
fbiA 3641447 p.Thr302Met missense_variant 0.99
fbiB 3641955 p.Gly141Arg missense_variant 0.27
rpoA 3877553 p.Glu319Lys missense_variant 1.0
rpoA 3878238 p.Asp90Glu missense_variant 0.16
clpC1 4038857 c.1848C>A synonymous_variant 0.13
clpC1 4039932 p.Gly258Val missense_variant 0.21
embC 4240897 c.1035C>G synonymous_variant 1.0
embC 4241456 p.Ala532Pro missense_variant 0.38
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embC 4242803 p.Val981Leu missense_variant 1.0
embC 4242822 p.Val987Gly missense_variant 0.39
embC 4242827 p.Leu989Val missense_variant 0.22
embA 4244118 p.Tyr296His missense_variant 1.0
embB 4249408 c.2895G>A synonymous_variant 1.0
ubiA 4269880 c.-48dupG upstream_gene_variant 1.0
ethA 4327672 c.-199G>A upstream_gene_variant 0.26
ethA 4328330 c.-858_-857insGC upstream_gene_variant 0.9
whiB6 4338595 c.-75delG upstream_gene_variant 1.0