Run ID: SRR1048986
Sample name:
Date: 02-04-2023 17:50:48
Number of reads: 757075
Percentage reads mapped: 21.64
Strain: lineage2.2.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155693 | p.Ser140Asn | missense_variant | 0.52 | isoniazid |
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 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.25 |
rpoC | 762893 | c.-477C>T | upstream_gene_variant | 0.35 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.32 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.44 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.44 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.41 |
rpoB | 762925 | p.Thr1040Ile | missense_variant | 0.41 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.41 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.4 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.4 |
rpoC | 762965 | c.-405T>C | upstream_gene_variant | 0.44 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.38 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.23 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763412 | p.Ala15Thr | missense_variant | 0.11 |
rpoC | 764329 | c.960C>T | synonymous_variant | 0.21 |
rpoC | 764338 | p.Glu323Asp | missense_variant | 0.3 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.32 |
rpoC | 764348 | p.Met327Leu | missense_variant | 0.32 |
rpoC | 764355 | p.Gln329Pro | missense_variant | 0.3 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.28 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.29 |
rpoC | 764383 | c.1014C>G | synonymous_variant | 0.29 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.3 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 0.32 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.29 |
rpoC | 764410 | c.1041G>T | synonymous_variant | 0.32 |
rpoC | 765891 | p.Arg841Leu | missense_variant | 0.11 |
rpoC | 765931 | c.2562C>T | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | 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 | 1303088 | p.Asp53Val | missense_variant | 0.18 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472264 | n.419T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472266 | n.421C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473038 | n.1193A>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473051 | n.1206T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473053 | n.1208T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473054 | n.1209C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473081 | n.1236C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473149 | n.1304G>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473162 | n.1317C>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475939 | n.2282G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476356 | n.2699C>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476384 | n.2727G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476428 | n.2771C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.29 |
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 | 2155600 | p.Cys171Val | missense_variant | 0.19 |
katG | 2155613 | p.Phe167Leu | missense_variant | 0.21 |
katG | 2155614 | c.498T>C | synonymous_variant | 0.21 |
katG | 2155617 | p.Ile165Met | missense_variant | 0.21 |
katG | 2155626 | c.486G>C | synonymous_variant | 0.3 |
katG | 2155637 | p.Leu159Ile | missense_variant | 0.35 |
katG | 2155641 | p.Lys157Arg | missense_variant | 0.35 |
katG | 2155650 | c.462G>A | synonymous_variant | 0.36 |
katG | 2155655 | p.Lys153Gln | missense_variant | 0.38 |
katG | 2155661 | p.Val151Ile | missense_variant | 0.35 |
katG | 2155668 | c.444G>C | synonymous_variant | 0.38 |
katG | 2155689 | c.421_423delTTGinsCTC | synonymous_variant | 0.5 |
katG | 2155704 | c.408C>T | synonymous_variant | 0.58 |
katG | 2155716 | c.396T>C | synonymous_variant | 0.58 |
katG | 2155722 | c.390G>C | synonymous_variant | 0.53 |
katG | 2155728 | c.384G>C | synonymous_variant | 0.53 |
katG | 2155735 | p.Met126Gln | missense_variant | 0.5 |
katG | 2155737 | c.375C>T | synonymous_variant | 0.47 |
katG | 2155741 | p.Gly124Ala | missense_variant | 0.47 |
katG | 2155743 | c.369G>T | synonymous_variant | 0.42 |
katG | 2155765 | p.His116Thr | missense_variant | 0.4 |
katG | 2155782 | c.330C>G | synonymous_variant | 0.29 |
katG | 2155785 | p.Ala109Ser | missense_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168445 | p.Pro723Leu | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518118 | p.Ser2Gly | missense_variant | 0.17 |
ahpC | 2726651 | c.459G>C | synonymous_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449435 | p.Ser311Leu | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568862 | c.-183C>T | upstream_gene_variant | 0.1 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3877575 | p.Ser311Arg | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242949 | c.-284C>T | upstream_gene_variant | 0.14 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethR | 4328081 | p.Met178Thr | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |