Run ID: ERR4816944
Sample name:
Date: 01-04-2023 14:43:06
Number of reads: 430001
Percentage reads mapped: 80.94
Strain: lineage2.2
Drug-resistance: RR-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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761142 | p.Lys446Gln | missense_variant | 0.33 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.29 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.48 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5378 | p.Trp47Arg | missense_variant | 0.13 |
gyrB | 5638 | c.399C>T | synonymous_variant | 0.15 |
gyrA | 7057 | c.-245C>T | upstream_gene_variant | 0.17 |
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 | 575881 | p.His178Gln | missense_variant | 0.15 |
rpoB | 760577 | p.Glu257Asp | missense_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.31 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.27 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.25 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.25 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.24 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.25 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.25 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.31 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.31 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.31 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.25 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.25 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.22 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.12 |
rpoC | 764274 | p.Phe302Ser | missense_variant | 0.15 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.14 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.13 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.14 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 779309 | p.Arg107His | missense_variant | 0.2 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417109 | p.Arg80His | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473122 | n.1281delA | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.29 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.15 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.14 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.17 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.17 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.14 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.13 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.12 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.12 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101741 | c.1302G>A | synonymous_variant | 0.17 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155090 | p.Trp341Leu | missense_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222263 | p.Arg301Leu | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289519 | c.-278T>C | upstream_gene_variant | 0.17 |
ahpC | 2726226 | p.Ala12Thr | missense_variant | 0.12 |
Rv2752c | 3066214 | c.-23G>T | upstream_gene_variant | 0.17 |
ald | 3086681 | c.-139T>C | upstream_gene_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3841562 | c.-142A>G | upstream_gene_variant | 1.0 |
clpC1 | 4039592 | c.1113G>A | synonymous_variant | 1.0 |
embC | 4241478 | p.Ala539Asp | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4269129 | c.-293G>C | upstream_gene_variant | 0.18 |
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 |