TB-Profiler result

Run: SRR5818411

Summary

Run ID: SRR5818411

Sample name:

Date: 04-04-2023 11:23:37

Number of reads: 123156

Percentage reads mapped: 93.62

Strain: lineage4.9

Drug-resistance: MDR-TB


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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
lineage4.9 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
rpoB 761155 p.Ser450Leu missense_variant 0.39 rifampicin
rpsL 781687 p.Lys43Arg missense_variant 0.18 streptomycin
rrs 1472644 n.799C>T non_coding_transcript_exon_variant 0.29 streptomycin
katG 2155168 p.Ser315Thr missense_variant 1.0 isoniazid
pncA 2288920 p.Gly108Arg missense_variant 0.61 pyrazinamide
embB 4247730 p.Gly406Ala missense_variant 0.34 ethambutol
gid 4408087 c.115delC frameshift_variant 0.43 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
gyrA 7585 p.Ser95Thr missense_variant 1.0
rrs 1472119 n.274G>A non_coding_transcript_exon_variant 0.17
rrs 1472150 n.305T>A non_coding_transcript_exon_variant 0.88
rrs 1472172 n.327T>C non_coding_transcript_exon_variant 0.87
rrs 1472251 n.406G>A non_coding_transcript_exon_variant 0.94
rrs 1472282 n.437T>G non_coding_transcript_exon_variant 0.86
rrs 1472284 n.439C>T non_coding_transcript_exon_variant 0.86
rrs 1472286 n.441C>G non_coding_transcript_exon_variant 0.87
rrs 1472293 n.448C>A non_coding_transcript_exon_variant 0.87
rrs 1472297 n.453_465delGTCCGGGTTCTCT non_coding_transcript_exon_variant 0.88
rrs 1472315 n.470T>G non_coding_transcript_exon_variant 0.86
rrs 1472328 n.483G>C non_coding_transcript_exon_variant 0.87
rrs 1472332 n.487A>G non_coding_transcript_exon_variant 0.87
rrs 1472333 n.488G>A non_coding_transcript_exon_variant 0.87
rrs 1472338 n.493A>G non_coding_transcript_exon_variant 0.88
rrs 1472344 n.499C>T non_coding_transcript_exon_variant 0.88
rrs 1472379 n.534T>C non_coding_transcript_exon_variant 0.8
rrs 1472400 n.555C>T non_coding_transcript_exon_variant 0.65
rrs 1472412 n.567A>G non_coding_transcript_exon_variant 0.36
rrs 1472416 n.571C>T non_coding_transcript_exon_variant 0.45
rrs 1472422 n.577T>C non_coding_transcript_exon_variant 0.42
rrs 1472427 n.582T>G non_coding_transcript_exon_variant 0.18
rrs 1472435 n.590T>C non_coding_transcript_exon_variant 0.41
rrs 1472436 n.591G>T non_coding_transcript_exon_variant 0.41
rrs 1472437 n.592T>G non_coding_transcript_exon_variant 0.41
rrs 1472438 n.593T>C non_coding_transcript_exon_variant 0.4
rrs 1472448 n.603T>C non_coding_transcript_exon_variant 0.41
rrs 1472449 n.604C>T non_coding_transcript_exon_variant 0.4
rrs 1472450 n.605A>C non_coding_transcript_exon_variant 0.4
rrs 1472451 n.606C>T non_coding_transcript_exon_variant 0.4
rrs 1472462 n.617T>G non_coding_transcript_exon_variant 0.44
rrs 1472464 n.619A>G non_coding_transcript_exon_variant 0.45
rrs 1472473 n.628G>T non_coding_transcript_exon_variant 0.47
rrs 1472474 n.629C>G non_coding_transcript_exon_variant 0.48
rrs 1472476 n.631A>G non_coding_transcript_exon_variant 0.49
rrs 1472486 n.641A>G non_coding_transcript_exon_variant 0.25
rrs 1472489 n.644A>T non_coding_transcript_exon_variant 0.4
rrs 1472494 n.649A>G non_coding_transcript_exon_variant 0.67
rrs 1472496 n.651T>G non_coding_transcript_exon_variant 0.6
rrs 1472498 n.653C>T non_coding_transcript_exon_variant 0.72
rrs 1472513 n.668T>C non_coding_transcript_exon_variant 0.42
rrs 1472581 n.736A>C non_coding_transcript_exon_variant 0.62
rrs 1472584 n.739A>T non_coding_transcript_exon_variant 0.48
rrs 1472597 n.752G>A non_coding_transcript_exon_variant 0.28
rrs 1472607 n.762G>A non_coding_transcript_exon_variant 0.31
rrs 1472647 n.802C>T non_coding_transcript_exon_variant 0.26
rrs 1472655 n.810G>T non_coding_transcript_exon_variant 0.67
rrs 1472660 n.815T>C non_coding_transcript_exon_variant 0.65
rrs 1472692 n.847T>C non_coding_transcript_exon_variant 0.57
rrs 1472714 n.869A>G non_coding_transcript_exon_variant 0.57
rrl 1475937 n.2280A>T non_coding_transcript_exon_variant 0.43
rrl 1475943 n.2286G>A non_coding_transcript_exon_variant 0.43
rrl 1475952 n.2295A>G non_coding_transcript_exon_variant 0.35
rrl 1475963 n.2306G>T non_coding_transcript_exon_variant 0.24
rrl 1475970 n.2313C>T non_coding_transcript_exon_variant 0.22
rrl 1475975 n.2318C>T non_coding_transcript_exon_variant 0.2
rrl 1475977 n.2320A>G non_coding_transcript_exon_variant 0.21
rrl 1475978 n.2321C>T non_coding_transcript_exon_variant 0.16
rrl 1475988 n.2331A>G non_coding_transcript_exon_variant 0.18
rrl 1476131 n.2474C>T non_coding_transcript_exon_variant 0.21
rrl 1476164 n.2507A>G non_coding_transcript_exon_variant 0.26
rrl 1476179 n.2522C>T non_coding_transcript_exon_variant 0.2
rrl 1476194 n.2537A>G non_coding_transcript_exon_variant 0.25
rrl 1476200 n.2543A>T non_coding_transcript_exon_variant 0.33
rrl 1476207 n.2550T>C non_coding_transcript_exon_variant 0.17
rrl 1476214 n.2557G>T non_coding_transcript_exon_variant 0.35
rrl 1476215 n.2558C>T non_coding_transcript_exon_variant 0.36
rrl 1476224 n.2567A>G non_coding_transcript_exon_variant 0.39
rrl 1476245 n.2588C>T non_coding_transcript_exon_variant 0.28
rrl 1476252 n.2595T>G non_coding_transcript_exon_variant 0.38
rrl 1476253 n.2596A>G non_coding_transcript_exon_variant 0.2
rrl 1476256 n.2599A>G non_coding_transcript_exon_variant 0.37
rrl 1476260 n.2603A>G non_coding_transcript_exon_variant 0.36
rrl 1476281 n.2624T>C non_coding_transcript_exon_variant 0.3
rrl 1476294 n.2637A>G non_coding_transcript_exon_variant 0.17
rrl 1476295 n.2638C>G non_coding_transcript_exon_variant 0.16
rrl 1476297 n.2640C>A non_coding_transcript_exon_variant 0.15
rrl 1476308 n.2651G>C non_coding_transcript_exon_variant 0.17
rrl 1476311 n.2654G>C non_coding_transcript_exon_variant 0.18
rrl 1476312 n.2655T>C non_coding_transcript_exon_variant 0.2
tlyA 1917972 c.33A>G synonymous_variant 1.0
tlyA 1918474 p.Pro179Ser missense_variant 0.33
ahpC 2726184 c.-9A>C upstream_gene_variant 0.25
ethA 4326173 p.Phe434Ser missense_variant 0.14
ethA 4326764 p.Ala237Val missense_variant 0.22