Run ID: SRR5818394
Sample name:
Date: 04-04-2023 11:17:04
Number of reads: 227932
Percentage reads mapped: 94.61
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.94 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1471929 | n.84C>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472119 | n.274G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472286 | n.441C>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472297 | n.453_461delGTCCGGGTT | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472309 | n.464C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472311 | n.466C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472312 | n.468_470delGAT | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472328 | n.483G>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476595 | n.2938C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476602 | n.2945G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476608 | n.2951C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ahpC | 2726184 | c.-9A>C | upstream_gene_variant | 0.35 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.4 |
ethA | 4326148 | c.1326G>T | synonymous_variant | 0.34 |
ethA | 4326439 | p.Asn345Lys | missense_variant | 0.31 |
ethA | 4326764 | p.Ala237Val | missense_variant | 0.28 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.36 |
gid | 4407742 | p.Arg154Pro | missense_variant | 0.17 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.17 |