TB-Profiler result

Run: SRR1049022
Summary

Run ID: SRR1049022

Sample name:

Date: 02-04-2023 17:51:44

Number of reads: 131178

Percentage reads mapped: 4.31

Strain: lineage4.9;lineage2

Drug-resistance: HR-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 0.11
lineage4.9 Euro-American (H37Rv-like) T1 None 0.82
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
katG 2155693 p.Ser140Asn missense_variant 1.0 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 9304 p.Gly668Asp missense_variant 1.0
fgd1 490608 c.-174delG upstream_gene_variant 1.0
fgd1 491742 c.960T>C synonymous_variant 1.0
rpoC 762893 c.-477C>T upstream_gene_variant 0.6
rpoC 762896 c.-474G>C upstream_gene_variant 0.73
rpoC 762917 c.-453C>G upstream_gene_variant 0.75
rpoC 762920 c.-450C>T upstream_gene_variant 0.75
rpoC 762923 c.-447C>G upstream_gene_variant 0.75
rpoB 762925 p.Thr1040Ile missense_variant 0.75
rpoC 762929 c.-441G>T upstream_gene_variant 0.82
rpoB 762939 p.Met1045Leu missense_variant 0.82
rpoB 762942 p.Ile1046Val missense_variant 0.82
rpoC 762965 c.-405T>C upstream_gene_variant 0.75
rpoC 762980 c.-390T>C upstream_gene_variant 0.62
rpoC 762989 c.-381G>C upstream_gene_variant 0.44
rpoC 763031 c.-339T>C upstream_gene_variant 1.0
rpoC 764329 c.960C>T synonymous_variant 0.83
rpoC 764338 p.Glu323Asp missense_variant 0.71
rpoC 764344 c.975C>T synonymous_variant 0.71
rpoC 764348 p.Met327Leu missense_variant 0.75
rpoC 764355 p.Gln329Pro missense_variant 0.75
rpoC 764377 c.1008C>G synonymous_variant 0.75
rpoC 764380 c.1011G>C synonymous_variant 0.75
rpoC 764383 c.1014C>G synonymous_variant 0.75
rpoC 764387 c.1018_1020delTTGinsCTC synonymous_variant 0.75
rpoC 764398 c.1029G>C synonymous_variant 0.75
rpoC 764405 c.1036_1038delAGGinsCGC synonymous_variant 0.75
rpoC 764410 c.1041G>T synonymous_variant 0.75
mmpL5 775639 p.Ile948Val missense_variant 1.0
mmpL5 776100 p.Thr794Ile missense_variant 1.0
mmpS5 779615 c.-710C>G upstream_gene_variant 1.0
rpsL 781395 c.-165T>C upstream_gene_variant 1.0
fbiC 1305297 c.2367G>C synonymous_variant 0.5
rrs 1471659 n.-187C>T upstream_gene_variant 1.0
rrs 1472160 n.315C>T non_coding_transcript_exon_variant 1.0
rrs 1472172 n.327T>C non_coding_transcript_exon_variant 0.75
rrs 1472181 n.336G>A non_coding_transcript_exon_variant 0.83
rrs 1472214 n.369C>G non_coding_transcript_exon_variant 0.89
rrs 1472235 n.390G>C non_coding_transcript_exon_variant 0.89
rrs 1472240 n.395G>C non_coding_transcript_exon_variant 0.89
rrs 1472242 n.397C>T non_coding_transcript_exon_variant 0.89
rrs 1472251 n.406G>A non_coding_transcript_exon_variant 0.88
rrs 1472253 n.408G>T non_coding_transcript_exon_variant 0.86
rrs 1472259 n.414C>A non_coding_transcript_exon_variant 0.86
rrs 1472264 n.419T>C non_coding_transcript_exon_variant 0.83
rrs 1472266 n.421C>A non_coding_transcript_exon_variant 0.83
rrs 1472277 n.432C>G non_coding_transcript_exon_variant 1.0
rrs 1472707 n.862A>T non_coding_transcript_exon_variant 0.6
rrs 1472713 n.868T>C non_coding_transcript_exon_variant 0.6
rrs 1472715 n.870C>T non_coding_transcript_exon_variant 0.6
rrs 1472716 n.871C>T non_coding_transcript_exon_variant 0.6
rrs 1472734 n.889C>T non_coding_transcript_exon_variant 0.82
rrs 1472741 n.896G>A non_coding_transcript_exon_variant 0.75
rrs 1472742 n.897C>T non_coding_transcript_exon_variant 0.75
rrs 1472781 n.936C>T non_coding_transcript_exon_variant 0.82
rrs 1472793 n.948A>T non_coding_transcript_exon_variant 0.89
rrs 1472803 n.958T>C non_coding_transcript_exon_variant 0.83
rrs 1472812 n.967A>C non_coding_transcript_exon_variant 0.83
rrs 1473145 n.1300C>T non_coding_transcript_exon_variant 1.0
rrs 1473149 n.1304G>C non_coding_transcript_exon_variant 1.0
rrs 1473162 n.1317C>G non_coding_transcript_exon_variant 1.0
rrs 1473166 n.1321G>A non_coding_transcript_exon_variant 1.0
rrs 1473173 n.1328C>T non_coding_transcript_exon_variant 0.89
rrs 1473177 n.1332G>A non_coding_transcript_exon_variant 0.89
rrs 1473191 n.1346C>T non_coding_transcript_exon_variant 0.8
rrs 1473192 n.1347A>G non_coding_transcript_exon_variant 0.8
rrs 1473199 n.1356delA non_coding_transcript_exon_variant 0.8
rrs 1473205 n.1360T>C non_coding_transcript_exon_variant 0.8
rrs 1473206 n.1361G>A non_coding_transcript_exon_variant 0.8
rrl 1474825 n.1168G>A non_coding_transcript_exon_variant 1.0
rrl 1474828 n.1171G>C non_coding_transcript_exon_variant 1.0
rrl 1474832 n.1176delG non_coding_transcript_exon_variant 1.0
rrl 1474864 n.1207C>T non_coding_transcript_exon_variant 1.0
rrl 1474869 n.1212G>T non_coding_transcript_exon_variant 0.67
rrl 1474875 n.1218G>A non_coding_transcript_exon_variant 0.67
rrl 1474876 n.1219T>A non_coding_transcript_exon_variant 0.67
rrl 1474883 n.1226T>C non_coding_transcript_exon_variant 0.67
rrl 1475499 n.1842C>G non_coding_transcript_exon_variant 1.0
rrl 1475516 n.1859T>A non_coding_transcript_exon_variant 0.67
rrl 1475518 n.1861A>T non_coding_transcript_exon_variant 0.5
rrl 1475526 n.1869C>T non_coding_transcript_exon_variant 0.4
rrl 1475538 n.1881T>C non_coding_transcript_exon_variant 0.33
rrl 1475539 n.1882A>T non_coding_transcript_exon_variant 0.33
rrl 1475540 n.1883C>T non_coding_transcript_exon_variant 0.33
rrl 1475545 n.1888T>G non_coding_transcript_exon_variant 0.33
rrl 1475553 n.1896G>T non_coding_transcript_exon_variant 0.33
rrl 1475555 n.1898T>G non_coding_transcript_exon_variant 0.33
rrl 1475570 n.1913A>T non_coding_transcript_exon_variant 0.33
rrl 1475571 n.1914A>T non_coding_transcript_exon_variant 0.33
rrl 1475573 n.1916G>A non_coding_transcript_exon_variant 0.33
rrl 1475576 n.1919C>T non_coding_transcript_exon_variant 0.33
rrl 1475791 n.2134A>G non_coding_transcript_exon_variant 0.75
rrl 1475803 n.2146T>C non_coding_transcript_exon_variant 0.75
rrl 1475804 n.2147G>C non_coding_transcript_exon_variant 0.75
rrl 1475816 n.2159C>G non_coding_transcript_exon_variant 0.83
rrl 1475817 n.2160A>G non_coding_transcript_exon_variant 0.83
rrl 1475874 n.2217C>T non_coding_transcript_exon_variant 1.0
rrl 1475881 n.2224T>C non_coding_transcript_exon_variant 1.0
rrl 1475883 n.2226A>C non_coding_transcript_exon_variant 1.0
rrl 1475884 n.2227A>G non_coding_transcript_exon_variant 1.0
rrl 1475892 n.2235A>C non_coding_transcript_exon_variant 1.0
rrl 1475894 n.2237C>A non_coding_transcript_exon_variant 1.0
rrl 1476336 n.2679C>G non_coding_transcript_exon_variant 0.73
rrl 1476356 n.2699C>G non_coding_transcript_exon_variant 0.85
rrl 1476357 n.2700T>A non_coding_transcript_exon_variant 0.85
rrl 1476358 n.2701T>C non_coding_transcript_exon_variant 0.85
rrl 1476359 n.2702C>G non_coding_transcript_exon_variant 0.86
rrl 1476381 n.2724G>C non_coding_transcript_exon_variant 0.89
rrl 1476382 n.2725A>G non_coding_transcript_exon_variant 0.89
rrl 1476384 n.2727G>C non_coding_transcript_exon_variant 0.89
rrl 1476408 n.2751G>A non_coding_transcript_exon_variant 0.95
rrl 1476411 n.2754G>A non_coding_transcript_exon_variant 0.91
rrl 1476428 n.2771C>A non_coding_transcript_exon_variant 0.94
rrl 1476443 n.2786G>C non_coding_transcript_exon_variant 0.8
rrl 1476455 n.2798C>G non_coding_transcript_exon_variant 0.69
rrl 1476463 n.2806C>T non_coding_transcript_exon_variant 0.5
rrl 1476466 n.2809C>T non_coding_transcript_exon_variant 0.45
rrl 1476470 n.2813C>T non_coding_transcript_exon_variant 0.45
rrl 1476481 n.2824T>C non_coding_transcript_exon_variant 0.45
rrl 1476506 n.2849T>C non_coding_transcript_exon_variant 0.22
rrl 1476512 n.2855C>T non_coding_transcript_exon_variant 0.25
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
ndh 2103097 c.-55C>G upstream_gene_variant 1.0
katG 2154724 p.Arg463Leu missense_variant 1.0
katG 2155600 p.Cys171Val missense_variant 1.0
katG 2155613 p.Phe167Leu missense_variant 1.0
katG 2155614 c.498T>C synonymous_variant 1.0
katG 2155617 p.Ile165Met missense_variant 1.0
katG 2155626 c.486G>C synonymous_variant 1.0
katG 2155637 p.Leu159Ile missense_variant 1.0
katG 2155641 p.Lys157Arg missense_variant 1.0
katG 2155650 c.462G>A synonymous_variant 1.0
katG 2155655 p.Lys153Gln missense_variant 1.0
katG 2155661 p.Val151Ile missense_variant 1.0
katG 2155668 c.444G>C synonymous_variant 1.0
katG 2155689 c.421_423delTTGinsCTC synonymous_variant 1.0
katG 2155704 c.408C>T synonymous_variant 1.0
katG 2155716 c.396T>C synonymous_variant 1.0
katG 2155722 c.390G>C synonymous_variant 1.0
katG 2155728 c.384G>C synonymous_variant 0.86
katG 2155735 p.Met126Gln missense_variant 0.86
katG 2155737 c.375C>T synonymous_variant 0.86
katG 2155741 p.Gly124Ala missense_variant 0.86
katG 2155743 c.369G>T synonymous_variant 0.86
katG 2155765 p.His116Thr missense_variant 0.57
PPE35 2167926 p.Leu896Ser missense_variant 1.0
Rv1979c 2223293 c.-129A>G upstream_gene_variant 1.0
Rv1979c 2223333 c.-171_-170delAG upstream_gene_variant 0.67
Rv2752c 3065617 p.Gly192Ala missense_variant 0.67
fprA 3473996 c.-11_-10insA upstream_gene_variant 1.0
clpC1 4040032 p.Val225Ile missense_variant 0.4
clpC1 4040066 c.639G>C synonymous_variant 0.33
clpC1 4040069 c.636G>C synonymous_variant 0.4
clpC1 4040072 c.633C>T synonymous_variant 0.4
embA 4242643 c.-590C>T upstream_gene_variant 1.0
embA 4243460 c.228C>T synonymous_variant 1.0
embA 4244926 p.Phe565Ser missense_variant 0.67
aftB 4267647 p.Asp397Gly missense_variant 1.0
gid 4407588 c.615A>G synonymous_variant 1.0