Run ID: SRR12199485
Sample name:
Date: 03-04-2023 06:43:13
Number of reads: 179900
Percentage reads mapped: 91.3
Strain: lineage2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.18 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5156 | c.-84G>A | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8386 | p.Ile362Thr | missense_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491661 | c.879C>T | synonymous_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 619781 | c.-110T>C | upstream_gene_variant | 0.33 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.22 |
rpoB | 760222 | p.Gly139Val | missense_variant | 0.15 |
rpoB | 760445 | c.639C>A | synonymous_variant | 0.13 |
rpoB | 763006 | p.Cys1067Tyr | missense_variant | 0.29 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763083 | p.Arg1093Ser | missense_variant | 0.27 |
rpoC | 763501 | p.Asp44Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.25 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.25 |
mmpS5 | 778626 | c.279_280insGTGAGCG | frameshift_variant | 0.4 |
mmpS5 | 778630 | p.Leu92Phe | missense_variant | 0.4 |
mmpS5 | 778632 | c.267_273delGCTCACC | frameshift_variant | 0.4 |
mmpR5 | 779437 | p.Val150Ile | missense_variant | 0.29 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781557 | c.-3T>G | upstream_gene_variant | 0.33 |
rplC | 801024 | c.216C>A | synonymous_variant | 0.33 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406894 | c.447C>A | synonymous_variant | 0.4 |
embR | 1417053 | p.Pro99Ser | missense_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472607 | n.762G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472608 | n.763T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475462 | n.1809delA | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475869 | n.2212C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476075 | n.2418_2419insGTCA | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476088 | n.2431A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476100 | n.2443A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476581 | n.2924G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673296 | c.-144T>C | upstream_gene_variant | 0.18 |
inhA | 1675000 | p.Gln267Lys | missense_variant | 0.25 |
rpsA | 1834084 | p.Asn181Lys | missense_variant | 0.5 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156251 | c.-140G>A | upstream_gene_variant | 0.22 |
katG | 2156508 | c.-397G>T | upstream_gene_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.5 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.5 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.4 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.4 |
Rv1979c | 2222126 | p.Asp347Tyr | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2725931 | c.-262T>C | upstream_gene_variant | 0.29 |
folC | 2746686 | p.Ala305Pro | missense_variant | 1.0 |
Rv2752c | 3065998 | p.Arg65His | missense_variant | 0.5 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339123 | p.Ser2Arg | missense_variant | 0.22 |
Rv3083 | 3449680 | p.Ala393Ser | missense_variant | 0.2 |
Rv3083 | 3449724 | p.Cys407* | stop_gained | 0.2 |
Rv3083 | 3449968 | c.1468delC | frameshift_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568796 | c.-117G>T | upstream_gene_variant | 0.5 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641648 | c.114G>A | synonymous_variant | 0.2 |
alr | 3841386 | p.Asn12Ser | missense_variant | 0.15 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.22 |
rpoA | 3877849 | p.Gly220Val | missense_variant | 0.2 |
clpC1 | 4038776 | p.Glu643Asp | missense_variant | 0.22 |
clpC1 | 4040010 | p.Ala232Arg | missense_variant | 0.22 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.25 |
embC | 4240762 | p.Met300Ile | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243136 | p.Arg1092Ser | missense_variant | 1.0 |
embA | 4243380 | p.Thr50Pro | missense_variant | 0.33 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244224 | p.Ala331Val | missense_variant | 0.5 |
embA | 4244347 | p.Trp372Leu | missense_variant | 0.33 |
embA | 4245275 | c.2043C>A | synonymous_variant | 0.2 |
embB | 4247925 | p.Arg471Leu | missense_variant | 0.29 |
aftB | 4267027 | p.Arg604Cys | missense_variant | 0.29 |
aftB | 4267191 | p.Gly549Val | missense_variant | 0.33 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269380 | p.Val152Phe | missense_variant | 0.2 |
ethA | 4327578 | c.-105C>T | upstream_gene_variant | 0.25 |
whiB6 | 4338566 | c.-45A>G | upstream_gene_variant | 0.12 |
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 |