Run ID: ERR4863405
Sample name:
Date: 01-04-2023 21:32:03
Number of reads: 4449346
Percentage reads mapped: 45.57
Strain: lineage4.1.2.1;lineage2.2.1
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.7 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.31 |
lineage4.1 | Euro-American | T;X;H | None | 0.25 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.64 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.68 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.33 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Gly | missense_variant | 0.54 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761095 | p.Leu430Pro | missense_variant | 0.65 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.64 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.49 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.15 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.6 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 0.72 | ethambutol |
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 | 491591 | p.Lys270Met | missense_variant | 0.37 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.63 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.44 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.78 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.4 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.11 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.61 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.31 |
rpoB | 760324 | p.Leu173Pro | missense_variant | 0.64 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.57 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.4 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.71 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.76 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.7 |
mmpL5 | 778292 | c.188dupC | frameshift_variant | 0.57 |
mmpR5 | 779243 | p.Val85Gly | missense_variant | 0.67 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.62 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.77 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476214 | n.2557G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.21 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.78 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.69 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.65 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.35 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.38 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288944 | p.Thr100Pro | missense_variant | 0.65 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.26 |
eis | 2715368 | c.-54_-37delGTCGTCGTAATATTCACG | upstream_gene_variant | 0.64 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.19 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.53 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.19 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.73 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.37 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.26 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.38 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.38 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.31 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.33 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.18 |
embB | 4247050 | c.537C>T | synonymous_variant | 0.31 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.79 |
ethA | 4326623 | p.Pro284Leu | missense_variant | 0.54 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.51 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.64 |