Run ID: ERR2509885
Sample name:
Date: 31-03-2023 18:32:50
Number of reads: 628273
Percentage reads mapped: 83.5
Strain: lineage3
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761098 | p.Ser431Thr | missense_variant | 0.11 | rifampicin |
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.14 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.56 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6981 | p.Ala581Val | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7445 | c.144C>T | synonymous_variant | 0.2 |
gyrA | 7446 | p.Lys49Glu | missense_variant | 0.2 |
gyrA | 7455 | p.His52Asn | missense_variant | 0.18 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8360 | c.1059G>A | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9623 | c.2322G>A | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.12 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.12 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.12 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.12 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.12 |
rpoB | 761088 | p.Ser428Cys | missense_variant | 0.11 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.11 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.11 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.14 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.13 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.14 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.11 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.14 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.19 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.17 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.17 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.12 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.12 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.1 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 777052 | p.Gly477Arg | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.21 |
fbiC | 1305073 | p.Ser715Cys | missense_variant | 0.11 |
embR | 1416426 | c.919_921delGCG | conservative_inframe_deletion | 0.16 |
embR | 1416436 | c.911_912insGTGGGT | disruptive_inframe_insertion | 0.16 |
embR | 1416440 | c.902_907delACCCAC | disruptive_inframe_deletion | 0.17 |
atpE | 1461082 | p.Gly13Ala | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475290 | n.1633A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.19 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169866 | c.747G>A | synonymous_variant | 0.11 |
Rv1979c | 2222273 | p.Ala298Ser | missense_variant | 1.0 |
Rv1979c | 2222826 | c.338dupT | frameshift_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.29 |
folC | 2746416 | p.Glu395Lys | missense_variant | 0.1 |
folC | 2747618 | c.-20A>G | upstream_gene_variant | 0.12 |
pepQ | 2859621 | c.797delC | frameshift_variant | 0.22 |
ribD | 2986752 | c.-87C>G | upstream_gene_variant | 1.0 |
Rv2752c | 3066219 | c.-28T>A | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087917 | c.1098C>G | synonymous_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474115 | p.Asp37Asn | missense_variant | 0.13 |
whiB7 | 3568665 | c.14_15insT | frameshift_variant | 1.0 |
Rv3236c | 3612568 | c.549G>C | synonymous_variant | 0.29 |
fbiA | 3640880 | c.340dupG | frameshift_variant | 0.12 |
fbiA | 3640888 | c.349delC | frameshift_variant | 0.13 |
alr | 3840211 | p.Glu404* | stop_gained | 1.0 |
alr | 3840688 | c.732delC | frameshift_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247358 | p.Val282Ala | missense_variant | 0.1 |
embB | 4249796 | p.Arg1095* | stop_gained | 0.2 |
aftB | 4268060 | c.777C>T | synonymous_variant | 0.14 |
ethR | 4327813 | p.Thr89Pro | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |