Run ID: ERR4819305
Sample name:
Date: 01-04-2023 16:02:09
Number of reads: 19367
Percentage reads mapped: 3.28
Strain: lineage4.9
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 1.0 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 761051 | c.1245G>C | synonymous_variant | 1.0 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 1.0 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
rpoB | 761066 | c.1260G>C | synonymous_variant | 1.0 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.9 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.9 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 1.0 |
rpoB | 761099 | c.1293C>T | synonymous_variant | 0.9 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.8 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
rpoB | 761147 | c.1341C>G | synonymous_variant | 0.67 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 1.0 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 1.0 |
rpoB | 762227 | c.2421G>A | synonymous_variant | 1.0 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 1.0 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 1.0 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 1.0 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 1.0 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 1.0 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 1.0 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 1.0 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 1.0 |
rpoC | 763511 | p.Cys48Gly | missense_variant | 1.0 |
rpoC | 763517 | p.Lys50Gln | missense_variant | 1.0 |
rpoC | 763528 | c.159G>C | synonymous_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763534 | c.165T>G | synonymous_variant | 1.0 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.83 |
rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.8 |
rpoC | 763598 | p.Arg77Lys | missense_variant | 0.67 |
rpoC | 763606 | c.237C>A | synonymous_variant | 0.67 |
rpoC | 763648 | c.279C>G | synonymous_variant | 1.0 |
rpoC | 763657 | p.Glu96Asp | missense_variant | 1.0 |
rpoC | 763660 | c.291T>C | synonymous_variant | 1.0 |
rpoC | 763675 | c.306C>G | synonymous_variant | 1.0 |
rpoC | 763696 | c.327T>A | synonymous_variant | 1.0 |
rpoC | 763699 | c.330G>T | synonymous_variant | 1.0 |
rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
rpoC | 763718 | p.Leu117Val | missense_variant | 1.0 |
rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 1.0 |
rpoC | 763729 | c.360G>C | synonymous_variant | 1.0 |
rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
rpoC | 763735 | c.366G>C | synonymous_variant | 1.0 |
rpoC | 763744 | c.375G>C | synonymous_variant | 1.0 |
rpoC | 763751 | p.Ile128Val | missense_variant | 1.0 |
rpoC | 763765 | c.396T>G | synonymous_variant | 1.0 |
rpoC | 763772 | p.Val135Met | missense_variant | 1.0 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 1.0 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 1.0 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 1.0 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 1.0 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
rpoC | 764527 | c.1158C>A | synonymous_variant | 1.0 |
rpoC | 764533 | c.1164C>A | synonymous_variant | 1.0 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 1.0 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 1.0 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 1.0 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 1.0 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 1.0 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 1.0 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
rpoC | 764582 | p.Leu405Met | missense_variant | 1.0 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 1.0 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 1.0 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 1.0 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 1.0 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 1.0 |
rpsL | 781643 | c.84G>C | synonymous_variant | 1.0 |
rpsL | 781652 | c.93T>C | synonymous_variant | 1.0 |
rpsL | 781655 | c.96T>C | synonymous_variant | 1.0 |
rpsL | 781658 | c.99A>G | synonymous_variant | 1.0 |
rpsL | 781682 | c.123T>G | synonymous_variant | 1.0 |
rpsL | 781703 | c.144G>T | synonymous_variant | 1.0 |
rpsL | 781706 | c.147T>G | synonymous_variant | 1.0 |
rpsL | 781709 | c.150G>A | synonymous_variant | 1.0 |
rpsL | 781745 | c.186G>A | synonymous_variant | 1.0 |
rpsL | 781751 | c.192G>C | synonymous_variant | 1.0 |
rpsL | 781754 | c.195G>A | synonymous_variant | 1.0 |
rpsL | 781760 | c.201T>C | synonymous_variant | 1.0 |
rpsL | 781766 | c.207C>T | synonymous_variant | 1.0 |
rpsL | 781796 | p.Met79Ile | missense_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 1.0 |
rpsL | 781835 | c.276T>C | synonymous_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473122 | n.1281delA | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 1.0 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474271 | n.614A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474551 | n.894G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475760 | n.2103C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475762 | n.2105G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476420 | n.2763G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 1.0 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 1.0 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 1.0 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 1.0 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 1.0 |
rpsA | 1833684 | p.Arg48His | missense_variant | 1.0 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 1.0 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 1.0 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 1.0 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 1.0 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 1.0 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 1.0 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 1.0 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 1.0 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 1.0 |
rpsA | 1834477 | c.936C>A | synonymous_variant | 1.0 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 1.0 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 1.0 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 1.0 |
rpsA | 1834522 | c.981C>T | synonymous_variant | 1.0 |
rpsA | 1834523 | p.Glu328Gln | missense_variant | 1.0 |
rpsA | 1834538 | p.Val333Leu | missense_variant | 1.0 |
fbiB | 3642710 | c.1176G>C | synonymous_variant | 1.0 |
fbiB | 3642711 | p.Leu393Val | missense_variant | 1.0 |
fbiB | 3642719 | c.1185T>C | synonymous_variant | 1.0 |
fbiB | 3642731 | c.1197C>G | synonymous_variant | 1.0 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 1.0 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 1.0 |
clpC1 | 4039981 | p.Leu242Ile | missense_variant | 1.0 |