TB-Profiler result

Run: SRR1049752
Summary

Run ID: SRR1049752

Sample name:

Date: 02-04-2023 18:24:19

Number of reads: 1581000

Percentage reads mapped: 36.7

Strain: lineage4.6.1.2

Drug-resistance: RR-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
lineage4.6 Euro-American T;LAM None 1.0
lineage4.6.1 Euro-American (Uganda) T2 RD724 0.99
lineage4.6.1.2 Euro-American T2 RD724 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 0.95 rifampicin
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 6501 p.Arg421His missense_variant 0.94
gyrA 7362 p.Glu21Gln missense_variant 1.0
gyrA 7539 p.Thr80Ala missense_variant 1.0
gyrA 7585 p.Ser95Thr missense_variant 1.0
gyrA 9304 p.Gly668Asp missense_variant 1.0
rpoC 762887 c.-483G>C upstream_gene_variant 0.12
rpoC 762899 c.-471G>C upstream_gene_variant 0.23
rpoC 762917 c.-453C>G upstream_gene_variant 0.22
rpoC 762920 c.-450C>T upstream_gene_variant 0.22
rpoC 762923 c.-447C>G upstream_gene_variant 0.21
rpoB 762925 p.Thr1040Ile missense_variant 0.21
rpoB 762934 c.3129_3130insAGCC frameshift_variant 0.2
rpoB 762938 c.3133_3136delATGA frameshift_variant 0.2
rpoC 762989 c.-381G>C upstream_gene_variant 0.13
rpoC 764410 c.1041G>C synonymous_variant 0.12
rpoC 764566 c.1197C>G synonymous_variant 0.17
rpoC 764575 c.1206T>G synonymous_variant 0.2
rpoC 764581 c.1212T>C synonymous_variant 0.21
rpoC 764582 p.Leu405Met missense_variant 0.23
rpoC 764587 c.1218C>G synonymous_variant 0.3
rpoC 764593 c.1224C>T synonymous_variant 0.33
rpoC 764605 c.1236G>C synonymous_variant 0.39
rpoC 764611 c.1242G>T synonymous_variant 0.41
rpoC 764632 c.1263T>C synonymous_variant 0.42
rpoC 764641 c.1272C>T synonymous_variant 0.44
rpoC 764650 c.1281G>T synonymous_variant 0.45
rpoC 764663 p.Val432Thr missense_variant 0.39
rpoC 764672 p.Gln435Glu missense_variant 0.37
rpoC 764677 c.1308C>G synonymous_variant 0.36
rpoC 764695 c.1326T>C synonymous_variant 0.23
rpoC 764701 c.1332C>G synonymous_variant 0.12
mmpL5 775639 p.Ile948Val missense_variant 1.0
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
embR 1416410 p.Leu313Arg missense_variant 0.97
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rrs 1472172 n.327T>C non_coding_transcript_exon_variant 0.41
rrs 1472214 n.369C>G non_coding_transcript_exon_variant 0.54
rrs 1472225 n.380C>A non_coding_transcript_exon_variant 0.49
rrs 1472235 n.390G>C non_coding_transcript_exon_variant 0.48
rrs 1472240 n.395G>A non_coding_transcript_exon_variant 0.48
rrs 1472242 n.397C>T non_coding_transcript_exon_variant 0.48
rrs 1472251 n.406G>A non_coding_transcript_exon_variant 0.41
rrs 1472253 n.408G>T non_coding_transcript_exon_variant 0.4
rrs 1472259 n.414C>A non_coding_transcript_exon_variant 0.37
rrs 1472264 n.419T>C non_coding_transcript_exon_variant 0.35
rrs 1472266 n.421C>A non_coding_transcript_exon_variant 0.34
rrs 1472277 n.432C>G non_coding_transcript_exon_variant 0.26
rrs 1472333 n.488G>T non_coding_transcript_exon_variant 0.2
rrs 1472338 n.493A>C non_coding_transcript_exon_variant 0.2
rrs 1472344 n.499C>T non_coding_transcript_exon_variant 0.22
rrs 1472349 n.504A>C non_coding_transcript_exon_variant 0.24
rrs 1472374 n.529T>G non_coding_transcript_exon_variant 0.24
rrs 1472379 n.534T>G non_coding_transcript_exon_variant 0.24
rrs 1472382 n.537G>T non_coding_transcript_exon_variant 0.24
rrs 1472391 n.546C>T non_coding_transcript_exon_variant 0.25
rrs 1472412 n.567A>C non_coding_transcript_exon_variant 0.21
rrs 1472415 n.570T>A non_coding_transcript_exon_variant 0.21
rrs 1472422 n.577T>C non_coding_transcript_exon_variant 0.21
rrs 1472714 n.869A>T non_coding_transcript_exon_variant 0.21
rrs 1472715 n.870C>A non_coding_transcript_exon_variant 0.21
rrs 1472716 n.871C>T non_coding_transcript_exon_variant 0.21
rrs 1472742 n.897C>T non_coding_transcript_exon_variant 0.44
rrs 1472770 n.925C>T non_coding_transcript_exon_variant 0.43
rrs 1472781 n.936C>T non_coding_transcript_exon_variant 0.44
rrs 1472793 n.948A>T non_coding_transcript_exon_variant 0.41
rrs 1472803 n.958T>A non_coding_transcript_exon_variant 0.34
rrs 1472812 n.967A>C non_coding_transcript_exon_variant 0.3
rrs 1472824 n.979T>A non_coding_transcript_exon_variant 0.19
rrs 1472826 n.981G>C non_coding_transcript_exon_variant 0.16
rrl 1474182 n.525C>G non_coding_transcript_exon_variant 0.2
rrl 1474184 n.527C>A non_coding_transcript_exon_variant 0.2
rrl 1474185 n.528G>C non_coding_transcript_exon_variant 0.2
rrl 1474199 n.542G>A non_coding_transcript_exon_variant 0.2
rrl 1474201 n.544T>C non_coding_transcript_exon_variant 0.21
rrl 1474218 n.561T>A non_coding_transcript_exon_variant 0.2
rrl 1474228 n.571T>C non_coding_transcript_exon_variant 0.19
rrl 1474249 n.592G>C non_coding_transcript_exon_variant 0.17
rrl 1475803 n.2146T>C non_coding_transcript_exon_variant 0.24
rrl 1475804 n.2147G>C non_coding_transcript_exon_variant 0.25
rrl 1475816 n.2159C>G non_coding_transcript_exon_variant 0.27
rrl 1475817 n.2160A>G non_coding_transcript_exon_variant 0.27
rrl 1475881 n.2224T>C non_coding_transcript_exon_variant 0.17
rrl 1475883 n.2226A>C non_coding_transcript_exon_variant 0.17
rrl 1476311 n.2654G>C non_coding_transcript_exon_variant 0.12
rrl 1476312 n.2655T>C non_coding_transcript_exon_variant 0.12
rrl 1476313 n.2656G>A non_coding_transcript_exon_variant 0.17
rrl 1476336 n.2679C>G non_coding_transcript_exon_variant 0.63
rrl 1476356 n.2699C>A non_coding_transcript_exon_variant 0.74
rrl 1476357 n.2700T>A non_coding_transcript_exon_variant 0.72
rrl 1476358 n.2701T>C non_coding_transcript_exon_variant 0.73
rrl 1476368 n.2711T>C non_coding_transcript_exon_variant 0.73
rrl 1476369 n.2712C>T non_coding_transcript_exon_variant 0.74
rrl 1476382 n.2725A>G non_coding_transcript_exon_variant 0.76
rrl 1476384 n.2727G>T non_coding_transcript_exon_variant 0.76
rrl 1476408 n.2751G>A non_coding_transcript_exon_variant 0.78
rrl 1476411 n.2754G>A non_coding_transcript_exon_variant 0.77
rrl 1476443 n.2786G>T non_coding_transcript_exon_variant 0.73
rrl 1476455 n.2798C>A non_coding_transcript_exon_variant 0.68
rrl 1476463 n.2806C>T non_coding_transcript_exon_variant 0.65
rrl 1476466 n.2809C>T non_coding_transcript_exon_variant 0.63
rrl 1476470 n.2813C>T non_coding_transcript_exon_variant 0.61
rrl 1476481 n.2824T>C non_coding_transcript_exon_variant 0.53
rrl 1476491 n.2834T>C non_coding_transcript_exon_variant 0.45
rrl 1476501 n.2844C>T non_coding_transcript_exon_variant 0.32
rrl 1476506 n.2849T>C non_coding_transcript_exon_variant 0.28
rrl 1476512 n.2855C>T non_coding_transcript_exon_variant 0.15
rrl 1476517 n.2860C>T non_coding_transcript_exon_variant 0.12
inhA 1674465 c.264C>T synonymous_variant 1.0
tlyA 1917972 c.33A>G synonymous_variant 1.0
katG 2154874 p.Tyr413Cys missense_variant 1.0
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
thyA 3073806 c.666C>G synonymous_variant 0.19
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embA 4245055 p.Thr608Asn missense_variant 1.0
ethR 4328183 p.Tyr212Cys missense_variant 1.0
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
whiB6 4338635 c.-114A>C upstream_gene_variant 1.0