Run ID: SRR8692897
Sample name:
Date: 13-08-2023 20:03:46
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.9
Drug-resistance: Other
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.84 | linezolid |
pncA | 2289039 | p.Trp68Leu | missense_variant | 0.13 | pyrazinamide |
pncA | 2289073 | p.His57Asp | missense_variant | 0.12 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5308 | c.69G>A | synonymous_variant | 0.33 |
gyrB | 6196 | c.957C>G | synonymous_variant | 0.12 |
gyrB | 6202 | c.963C>G | synonymous_variant | 0.13 |
gyrB | 6203 | p.Ser322Ala | missense_variant | 0.13 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.12 |
gyrB | 6215 | p.Ser326Thr | missense_variant | 0.12 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.12 |
gyrB | 6243 | p.Arg335Gln | missense_variant | 0.12 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.11 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.11 |
gyrB | 6365 | p.Gly376Cys | missense_variant | 0.2 |
gyrA | 8013 | p.Gln238Lys | missense_variant | 0.17 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.11 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.12 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.12 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 0.18 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.12 |
gyrA | 9324 | c.2023_2025delTCGinsAGC | synonymous_variant | 0.13 |
gyrA | 9335 | c.2034G>T | synonymous_variant | 0.12 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.12 |
fgd1 | 491245 | p.Tyr155His | missense_variant | 0.1 |
fgd1 | 491728 | p.Asp316Tyr | missense_variant | 0.15 |
rpoB | 760019 | c.213G>T | synonymous_variant | 0.13 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.15 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.15 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.15 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.17 |
rpoC | 762443 | c.-927G>C | upstream_gene_variant | 0.1 |
rpoC | 762449 | c.-921C>G | upstream_gene_variant | 0.11 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.1 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.16 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.23 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.22 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.17 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.18 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.19 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.19 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.19 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.18 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.18 |
rpoC | 763726 | c.357C>T | synonymous_variant | 0.18 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.12 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.12 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.12 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.13 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.12 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.14 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.13 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.14 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.14 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.14 |
rpoC | 766242 | p.Thr958Asn | missense_variant | 0.12 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.12 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.14 |
rpoC | 767106 | p.Asn1246Met | missense_variant | 0.14 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.23 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.24 |
rpoC | 767162 | p.Asn1265Ala | missense_variant | 0.19 |
rpoC | 767173 | c.3804C>G | synonymous_variant | 0.17 |
rpoC | 767174 | p.Asn1269Asp | missense_variant | 0.17 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.14 |
rpoC | 767185 | c.3816G>C | synonymous_variant | 0.13 |
rpoC | 767186 | p.Gln1273Asn | missense_variant | 0.13 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.12 |
rpoC | 767197 | c.3828G>A | synonymous_variant | 0.12 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.15 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.11 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.1 |
mmpL5 | 776210 | c.2271C>T | synonymous_variant | 0.12 |
mmpL5 | 776591 | c.1890C>A | synonymous_variant | 0.12 |
mmpL5 | 776734 | p.Ser583Gly | missense_variant | 0.11 |
mmpL5 | 777042 | p.Arg480Leu | missense_variant | 0.2 |
mmpL5 | 777083 | p.Asn466Lys | missense_variant | 0.15 |
mmpL5 | 778747 | c.-267C>A | upstream_gene_variant | 0.15 |
mmpS5 | 779509 | c.-604G>T | upstream_gene_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.11 |
rplC | 800651 | c.-158G>C | upstream_gene_variant | 0.15 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.84 |
atpE | 1460952 | c.-93T>C | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471834 | n.-12G>T | upstream_gene_variant | 0.18 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472290 | n.445C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472324 | n.479G>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472573 | n.728C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473165 | n.1320C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473239 | n.1394G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473811 | n.154C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473961 | n.304G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474340 | n.683C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474792 | n.1135C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474895 | n.1238C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475202 | n.1545G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475209 | n.1552G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475221 | n.1564C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475961 | n.2304C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476003 | n.2346T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476512 | n.2855C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476576 | n.2919C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476777 | n.3120C>A | non_coding_transcript_exon_variant | 0.22 |
inhA | 1673387 | c.-815C>A | upstream_gene_variant | 0.13 |
rpsA | 1833616 | c.75A>G | synonymous_variant | 0.14 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.14 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.14 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.14 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.2 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.17 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.15 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.14 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.14 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.13 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.12 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.12 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.12 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.13 |
rpsA | 1834299 | p.Gln253Pro | missense_variant | 0.11 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.11 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.11 |
rpsA | 1834585 | c.1044C>A | synonymous_variant | 0.13 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.14 |
PPE35 | 2168872 | c.1741C>T | synonymous_variant | 0.13 |
PPE35 | 2168912 | c.1701G>T | synonymous_variant | 0.17 |
PPE35 | 2168939 | p.Leu558Phe | missense_variant | 0.14 |
PPE35 | 2169866 | c.747G>T | synonymous_variant | 0.17 |
Rv1979c | 2222020 | p.Arg382Gln | missense_variant | 0.14 |
Rv1979c | 2222257 | p.Ile303Thr | missense_variant | 0.13 |
Rv1979c | 2222391 | c.774C>A | synonymous_variant | 0.18 |
Rv1979c | 2222541 | c.624T>C | synonymous_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.32 |
eis | 2715415 | c.-83C>A | upstream_gene_variant | 0.12 |
ald | 3086697 | c.-123G>T | upstream_gene_variant | 0.29 |
fbiB | 3642858 | p.Ala442Thr | missense_variant | 0.13 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.11 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.1 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.11 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.11 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.12 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.12 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.12 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.12 |
clpC1 | 4040666 | c.39C>A | synonymous_variant | 0.15 |
embC | 4241806 | c.1944G>A | synonymous_variant | 0.14 |
embA | 4245152 | c.1920C>A | synonymous_variant | 0.13 |
aftB | 4267084 | p.His585Asn | missense_variant | 0.12 |
ethA | 4327173 | p.His101Asn | missense_variant | 0.18 |