TB-Profiler result

Run: SRR13861518
Summary

Run ID: SRR13861518

Sample name:

Date: 03-04-2023 09:33:53

Number of reads: 2148896

Percentage reads mapped: 71.7

Strain: lineage4.9

Drug-resistance: Other

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
lineage4.9 Euro-American (H37Rv-like) T1 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
rrs 1472122 n.277G>C non_coding_transcript_exon_variant 1.0 streptomycin
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 5319 p.Arg27Leu missense_variant 1.0
rpoB 760867 p.Gly354Asp missense_variant 1.0
rpoB 762496 c.2691delC frameshift_variant 1.0
rpoC 764793 p.Met475Arg missense_variant 0.99
rpoC 766563 p.Thr1065Ser missense_variant 1.0
mmpL5 775976 c.2505G>C synonymous_variant 1.0
mmpL5 776814 p.Gln556Arg missense_variant 1.0
rplC 800623 c.-186A>C upstream_gene_variant 1.0
rplC 800769 c.-40A>T upstream_gene_variant 1.0
fbiC 1302878 c.-53C>G upstream_gene_variant 1.0
fbiC 1303535 p.Ser202Leu missense_variant 1.0
atpE 1461256 p.Met71Arg missense_variant 1.0
rrs 1471836 n.-10A>G upstream_gene_variant 1.0
rrs 1472655 n.810G>A non_coding_transcript_exon_variant 0.13
rrl 1476332 n.2675G>C non_coding_transcript_exon_variant 0.15
rrl 1476353 n.2696G>T non_coding_transcript_exon_variant 0.24
rrl 1476358 n.2701T>C non_coding_transcript_exon_variant 0.3
rrl 1476369 n.2712C>T non_coding_transcript_exon_variant 0.32
rrl 1476372 n.2715T>C non_coding_transcript_exon_variant 0.27
rrl 1476382 n.2725A>G non_coding_transcript_exon_variant 0.29
rrl 1476383 n.2726T>A non_coding_transcript_exon_variant 0.19
rrl 1476408 n.2751G>A non_coding_transcript_exon_variant 0.31
rrl 1476425 n.2768G>T non_coding_transcript_exon_variant 0.27
rrl 1476428 n.2771C>T non_coding_transcript_exon_variant 0.25
rrl 1476429 n.2772A>C non_coding_transcript_exon_variant 0.29
rrl 1476466 n.2809C>T non_coding_transcript_exon_variant 0.34
rrl 1476481 n.2824T>C non_coding_transcript_exon_variant 0.26
rrl 1476506 n.2849T>C non_coding_transcript_exon_variant 0.14
rrl 1476514 n.2857C>T non_coding_transcript_exon_variant 0.12
rrl 1476519 n.2862C>G non_coding_transcript_exon_variant 0.1
rrl 1476525 n.2868A>G non_coding_transcript_exon_variant 0.1
rrl 1476537 n.2880A>G non_coding_transcript_exon_variant 0.11
rrl 1476538 n.2881A>G non_coding_transcript_exon_variant 0.1
katG 2156157 c.-46C>A upstream_gene_variant 1.0
PPE35 2168627 p.Ile662Met missense_variant 1.0
Rv1979c 2222100 c.1065T>A synonymous_variant 1.0
pncA 2289242 c.-1T>C upstream_gene_variant 1.0
ribD 2987205 p.Ser123Ala missense_variant 1.0
ribD 2987347 p.Pro170Leu missense_variant 1.0
Rv3083 3448903 p.Asp134His missense_variant 0.99
clpC1 4039663 p.Gly348Ser missense_variant 0.99
embC 4241256 p.Arg465Thr missense_variant 1.0
embA 4246449 p.Val1073Phe missense_variant 1.0
aftB 4268192 c.645G>C synonymous_variant 1.0