Run ID: SRR5818402
Sample name:
Date: 04-04-2023 11:21:12
Number of reads: 315368
Percentage reads mapped: 98.54
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 | 0.4 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
mmpR5 | 779434 | p.Val149Ile | missense_variant | 0.99 |
rrs | 1472119 | n.274G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472436 | n.591G>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472486 | n.641A>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472571 | n.726G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472585 | n.740A>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476235 | n.2578A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476544 | n.2887T>C | non_coding_transcript_exon_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.98 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.98 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.99 |