TB-Profiler result

Run: SRR1013634
Summary

Run ID: SRR1013634

Sample name:

Date: 02-04-2023 16:02:15

Number of reads: 1244378

Percentage reads mapped: 22.08

Strain: lineage2.2

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
lineage2 East-Asian Beijing RD105 1.0
lineage2.2 East-Asian (Beijing) Beijing-RD207 RD105;RD207 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 761277 p.Ile491Phe missense_variant 0.94 rifampicin
katG 2155168 p.Ser315Thr missense_variant 1.0 isoniazid
katG 2155693 p.Ser140Asn missense_variant 0.36 isoniazid
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 9304 p.Gly668Asp missense_variant 1.0
fgd1 491742 c.960T>C synonymous_variant 1.0
rpoB 760480 p.Arg225Pro missense_variant 0.73
rpoB 762881 p.Met1025Ile missense_variant 0.19
rpoC 762893 c.-477C>T upstream_gene_variant 0.26
rpoC 762896 c.-474G>C upstream_gene_variant 0.26
rpoC 762917 c.-453C>G upstream_gene_variant 0.38
rpoC 762920 c.-450C>T upstream_gene_variant 0.36
rpoC 762923 c.-447C>G upstream_gene_variant 0.35
rpoB 762925 p.Thr1040Ile missense_variant 0.35
rpoC 762929 c.-441G>T upstream_gene_variant 0.34
rpoB 762939 p.Met1045Leu missense_variant 0.36
rpoB 762942 p.Ile1046Val missense_variant 0.38
rpoC 762965 c.-405T>C upstream_gene_variant 0.38
rpoC 762980 c.-390T>C upstream_gene_variant 0.31
rpoC 762989 c.-381G>C upstream_gene_variant 0.16
rpoC 763031 c.-339T>C upstream_gene_variant 1.0
rpoC 764338 p.Glu323Asp missense_variant 0.29
rpoC 764344 c.975C>T synonymous_variant 0.29
rpoC 764348 p.Met327Leu missense_variant 0.38
rpoC 764355 p.Gln329Pro missense_variant 0.43
rpoC 764377 c.1008C>G synonymous_variant 0.33
rpoC 764380 c.1011G>C synonymous_variant 0.33
rpoC 764383 c.1014C>G synonymous_variant 0.33
rpoC 764387 c.1018_1020delTTGinsCTC synonymous_variant 0.33
rpoC 764398 c.1029G>C synonymous_variant 0.33
rpoC 764405 c.1036_1038delAGGinsCGC synonymous_variant 0.3
rpoC 764410 c.1041G>T synonymous_variant 0.32
rpoC 764428 c.1059G>T synonymous_variant 0.26
rpoC 765599 p.Glu744Lys missense_variant 0.62
rpoC 765905 p.Val846Leu missense_variant 0.17
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 776100 p.Thr794Ile missense_variant 1.0
mmpS5 778656 p.Ala84Thr missense_variant 1.0
mmpS5 779615 c.-710C>G upstream_gene_variant 1.0
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
rpsL 781406 c.-154_-153insC upstream_gene_variant 1.0
fbiC 1303671 c.747_750dupCCGG frameshift_variant 0.25
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rrs 1472172 n.327T>C non_coding_transcript_exon_variant 0.12
rrs 1472181 n.336G>A non_coding_transcript_exon_variant 0.18
rrs 1472214 n.369C>G non_coding_transcript_exon_variant 0.3
rrs 1472235 n.390G>C non_coding_transcript_exon_variant 0.27
rrs 1472240 n.395G>C non_coding_transcript_exon_variant 0.27
rrs 1472242 n.397C>T non_coding_transcript_exon_variant 0.27
rrs 1472251 n.406G>A non_coding_transcript_exon_variant 0.23
rrs 1472253 n.408G>T non_coding_transcript_exon_variant 0.22
rrs 1472259 n.414C>A non_coding_transcript_exon_variant 0.19
rrs 1472264 n.419T>C non_coding_transcript_exon_variant 0.17
rrs 1472266 n.421C>A non_coding_transcript_exon_variant 0.17
rrs 1472277 n.432C>G non_coding_transcript_exon_variant 0.16
rrs 1472571 n.726G>C non_coding_transcript_exon_variant 0.11
rrs 1472574 n.729T>A non_coding_transcript_exon_variant 0.11
rrs 1472579 n.734G>C non_coding_transcript_exon_variant 0.11
rrs 1472581 n.736A>C non_coding_transcript_exon_variant 0.11
rrs 1472583 n.738T>A non_coding_transcript_exon_variant 0.11
rrs 1472584 n.739A>T non_coding_transcript_exon_variant 0.11
rrs 1472598 n.753A>C non_coding_transcript_exon_variant 0.12
rrs 1472599 n.754G>A non_coding_transcript_exon_variant 0.12
rrs 1472616 n.771G>A non_coding_transcript_exon_variant 0.13
rrs 1472734 n.889C>T non_coding_transcript_exon_variant 0.22
rrs 1472741 n.896G>A non_coding_transcript_exon_variant 0.24
rrs 1472742 n.897C>T non_coding_transcript_exon_variant 0.24
rrs 1472781 n.936C>T non_coding_transcript_exon_variant 0.28
rrs 1472793 n.948A>T non_coding_transcript_exon_variant 0.26
rrs 1472803 n.958T>C non_coding_transcript_exon_variant 0.2
rrs 1472812 n.967A>C non_coding_transcript_exon_variant 0.19
rrs 1473145 n.1300C>T non_coding_transcript_exon_variant 0.29
rrs 1473149 n.1304G>C non_coding_transcript_exon_variant 0.28
rrs 1473162 n.1317C>G non_coding_transcript_exon_variant 0.32
rrs 1473166 n.1321G>A non_coding_transcript_exon_variant 0.33
rrs 1473173 n.1328C>T non_coding_transcript_exon_variant 0.33
rrs 1473177 n.1332G>A non_coding_transcript_exon_variant 0.33
rrs 1473191 n.1346C>T non_coding_transcript_exon_variant 0.32
rrs 1473192 n.1347A>G non_coding_transcript_exon_variant 0.32
rrs 1473199 n.1356delA non_coding_transcript_exon_variant 0.31
rrs 1473205 n.1360T>C non_coding_transcript_exon_variant 0.3
rrs 1473206 n.1361G>A non_coding_transcript_exon_variant 0.31
rrl 1475803 n.2146T>C non_coding_transcript_exon_variant 0.11
rrl 1475804 n.2147G>C non_coding_transcript_exon_variant 0.11
rrl 1475816 n.2159C>G non_coding_transcript_exon_variant 0.17
rrl 1475817 n.2160A>G non_coding_transcript_exon_variant 0.17
rrl 1475874 n.2217C>T non_coding_transcript_exon_variant 0.15
rrl 1476336 n.2679C>G non_coding_transcript_exon_variant 0.37
rrl 1476356 n.2699C>G non_coding_transcript_exon_variant 0.43
rrl 1476357 n.2700T>A non_coding_transcript_exon_variant 0.43
rrl 1476358 n.2701T>C non_coding_transcript_exon_variant 0.43
rrl 1476359 n.2702C>G non_coding_transcript_exon_variant 0.43
rrl 1476381 n.2724G>C non_coding_transcript_exon_variant 0.52
rrl 1476382 n.2725A>G non_coding_transcript_exon_variant 0.52
rrl 1476384 n.2727G>C non_coding_transcript_exon_variant 0.5
rrl 1476408 n.2751G>A non_coding_transcript_exon_variant 0.58
rrl 1476411 n.2754G>A non_coding_transcript_exon_variant 0.61
rrl 1476428 n.2771C>A non_coding_transcript_exon_variant 0.54
rrl 1476443 n.2786G>C non_coding_transcript_exon_variant 0.42
rrl 1476455 n.2798C>G non_coding_transcript_exon_variant 0.4
rrl 1476463 n.2806C>T non_coding_transcript_exon_variant 0.33
rrl 1476466 n.2809C>T non_coding_transcript_exon_variant 0.28
rrl 1476470 n.2813C>T non_coding_transcript_exon_variant 0.27
rrl 1476481 n.2824T>C non_coding_transcript_exon_variant 0.28
rrl 1476506 n.2849T>C non_coding_transcript_exon_variant 0.14
rpsA 1833909 p.Asp123Ala missense_variant 1.0
rpsA 1834177 c.636A>C synonymous_variant 1.0
tlyA 1917972 c.33A>G synonymous_variant 1.0
katG 2154724 p.Arg463Leu missense_variant 1.0
katG 2155617 p.Ile165Met missense_variant 0.13
katG 2155626 c.486G>C synonymous_variant 0.19
katG 2155637 p.Leu159Ile missense_variant 0.22
katG 2155641 p.Lys157Arg missense_variant 0.24
katG 2155650 c.462G>A synonymous_variant 0.29
katG 2155655 p.Lys153Gln missense_variant 0.29
katG 2155661 p.Val151Ile missense_variant 0.27
katG 2155668 c.444G>C synonymous_variant 0.32
katG 2155689 c.421_423delTTGinsCTC synonymous_variant 0.36
katG 2155704 c.408C>T synonymous_variant 0.38
katG 2155716 c.396T>C synonymous_variant 0.38
katG 2155722 c.390G>C synonymous_variant 0.37
katG 2155728 c.384G>C synonymous_variant 0.35
katG 2155735 p.Met126Gln missense_variant 0.31
katG 2155737 c.375C>T synonymous_variant 0.33
katG 2155741 p.Gly124Ala missense_variant 0.36
katG 2155743 c.369G>T synonymous_variant 0.36
katG 2155765 p.His116Thr missense_variant 0.23
PPE35 2167926 p.Leu896Ser missense_variant 1.0
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
folC 2746165 c.1431_1433dupGGC disruptive_inframe_insertion 0.15
ald 3086788 c.-32T>C upstream_gene_variant 1.0
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
Rv3236c 3612813 p.Thr102Ala missense_variant 0.96
ddn 3987084 p.Gly81Ser missense_variant 1.0
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embA 4243460 c.228C>T synonymous_variant 1.0
embB 4247927 c.1414C>T synonymous_variant 1.0
aftB 4267647 p.Asp397Gly missense_variant 1.0
aftB 4267851 p.Gln329Arg missense_variant 0.11
ubiA 4269317 p.Ser173Ala missense_variant 0.6
whiB6 4338595 c.-75delG upstream_gene_variant 1.0
gid 4407588 c.615A>G synonymous_variant 1.0
gid 4407866 p.Glu113* stop_gained 1.0
gid 4407927 p.Glu92Asp missense_variant 1.0