Run ID: SRR5818466
Sample name:
Date: 04-04-2023 11:33:25
Number of reads: 253884
Percentage reads mapped: 94.25
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 | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.64 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472027 | n.183_189delACGGGAT | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472037 | n.192_193insCTTTAG | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472057 | n.212C>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472138 | n.293C>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472147 | n.302G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.92 |
ahpC | 2726184 | c.-9A>C | upstream_gene_variant | 0.51 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.26 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.93 |