Run ID: ERR3439268
Sample name:
Date: 01-04-2023 02:00:35
Number of reads: 27309
Percentage reads mapped: 2.3
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.98 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472518 | n.673G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472592 | n.747C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475752 | n.2095C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475776 | n.2119G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476420 | n.2763G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476433 | n.2776C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.3 |
folC | 2746345 | c.1254G>A | synonymous_variant | 0.67 |
clpC1 | 4038334 | p.Phe791Leu | missense_variant | 0.4 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |