Run ID: ERR4815551
Sample name:
Date: 01-04-2023 13:55:43
Number of reads: 744281
Percentage reads mapped: 44.26
Strain: lineage2.2.1
Drug-resistance: Other
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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.76 | streptomycin |
pncA | 2288844 | p.Ile133Thr | missense_variant | 0.12 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7391 | c.91_98delTATGCGAT | frameshift_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490986 | c.204G>T | synonymous_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576741 | p.Ala465Glu | missense_variant | 0.17 |
ccsA | 620194 | p.Thr102Ala | missense_variant | 0.25 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761435 | c.1629T>C | synonymous_variant | 0.14 |
rpoB | 761438 | c.1632G>T | synonymous_variant | 0.14 |
rpoB | 761441 | p.Asp545Glu | missense_variant | 0.14 |
rpoB | 761444 | c.1638T>C | synonymous_variant | 0.17 |
rpoB | 761447 | c.1641C>G | synonymous_variant | 0.15 |
rpoB | 761471 | c.1665C>G | synonymous_variant | 0.13 |
rpoB | 761483 | c.1677G>C | synonymous_variant | 0.11 |
rpoC | 762782 | c.-588T>C | upstream_gene_variant | 0.18 |
rpoB | 762799 | p.Ala998Gly | missense_variant | 0.12 |
rpoC | 762812 | c.-558C>G | upstream_gene_variant | 0.11 |
rpoB | 762813 | p.Met1003Val | missense_variant | 0.11 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.13 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.13 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.12 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.12 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.12 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.16 |
rpoC | 762956 | c.-414G>C | upstream_gene_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764939 | p.Leu524Met | missense_variant | 0.11 |
rpoC | 765236 | p.Asp623Asn | missense_variant | 0.12 |
rpoC | 766891 | c.3527delT | frameshift_variant | 0.15 |
rpoC | 766918 | c.3549C>A | synonymous_variant | 0.12 |
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 | 777704 | c.777G>A | synonymous_variant | 0.11 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.13 |
rpsL | 781667 | c.108C>T | synonymous_variant | 0.14 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.11 |
fbiC | 1303893 | c.963G>T | synonymous_variant | 0.17 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416847 | c.501A>T | synonymous_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473291 | n.1446G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473316 | n.1471C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473318 | n.1473G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474074 | n.417C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476252 | n.2595T>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.19 |
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 | 0.15 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.13 |
inhA | 1674210 | c.9A>C | synonymous_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917965 | p.Ala9Val | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917975 | c.36C>G | synonymous_variant | 0.22 |
tlyA | 1917981 | c.42G>C | synonymous_variant | 0.2 |
tlyA | 1917987 | c.48G>C | synonymous_variant | 0.22 |
tlyA | 1917996 | c.57A>C | synonymous_variant | 0.2 |
tlyA | 1918002 | p.Gln21His | missense_variant | 0.17 |
ndh | 2101843 | p.His400Gln | missense_variant | 0.12 |
ndh | 2102861 | p.Gly61Ala | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170050 | p.Ala188Glu | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289173 | c.69T>C | synonymous_variant | 0.5 |
kasA | 2518871 | p.His253Asn | missense_variant | 0.18 |
folC | 2746433 | p.Gly389Val | missense_variant | 0.14 |
Rv2752c | 3067030 | c.-839C>T | upstream_gene_variant | 0.14 |
thyX | 3067602 | p.Arg115Gln | missense_variant | 0.18 |
thyX | 3067750 | p.Asp66Asn | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087317 | c.498C>A | synonymous_variant | 0.15 |
Rv3083 | 3448426 | c.-78T>C | upstream_gene_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474882 | p.Asn292Lys | missense_variant | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3640803 | c.-732C>T | upstream_gene_variant | 1.0 |
fbiB | 3640920 | c.-615A>G | upstream_gene_variant | 0.17 |
fbiB | 3640989 | c.-546T>C | upstream_gene_variant | 0.14 |
fbiB | 3642865 | p.Leu444Ser | missense_variant | 0.18 |
alr | 3840256 | p.Glu389Lys | missense_variant | 0.12 |
clpC1 | 4038670 | p.Leu679Met | missense_variant | 0.11 |
clpC1 | 4039293 | p.Gly471Val | missense_variant | 0.13 |
clpC1 | 4039596 | p.His370Leu | missense_variant | 0.22 |
embC | 4239983 | p.Ala41Thr | missense_variant | 0.22 |
embC | 4241195 | p.Ser445Pro | missense_variant | 0.14 |
embC | 4241306 | p.Val482Ile | missense_variant | 0.14 |
embC | 4242331 | c.2474delG | frameshift_variant | 0.17 |
embA | 4242352 | c.-881G>C | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244513 | c.1281C>A | synonymous_variant | 0.29 |
embA | 4245536 | c.2307delC | frameshift_variant | 0.13 |
embB | 4245566 | c.-948C>T | upstream_gene_variant | 0.15 |
embB | 4245683 | c.-831C>T | upstream_gene_variant | 0.14 |
embA | 4245693 | p.Ile821Val | missense_variant | 0.31 |
embB | 4245714 | c.-800C>T | upstream_gene_variant | 0.18 |
embB | 4245725 | c.-789A>G | upstream_gene_variant | 0.18 |
embB | 4245726 | c.-788T>C | upstream_gene_variant | 0.18 |
embB | 4248461 | p.Ser650Pro | missense_variant | 0.12 |
embB | 4248633 | p.Val707Ala | missense_variant | 0.15 |
aftB | 4267265 | c.1572C>T | synonymous_variant | 0.11 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267704 | p.Leu378Pro | missense_variant | 0.13 |
ethA | 4328133 | c.-660C>T | upstream_gene_variant | 0.17 |
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 |