Run ID: ERR3468549
Sample name:
Date: 01-04-2023 02:17:21
Number of reads: 25939
Percentage reads mapped: 1.89
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 | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8741 | c.1440C>T | synonymous_variant | 1.0 |
gyrA | 9217 | p.Asp639Ala | missense_variant | 1.0 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472349 | n.504A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472374 | n.529T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472509 | n.664G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472517 | n.672T>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 | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472553 | n.708C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472572 | n.727T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472574 | n.729T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472583 | n.738T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472584 | n.739A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472594 | n.749G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1472697 | n.852T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472714 | n.869A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
thyX | 3067368 | p.Arg193Gln | missense_variant | 0.4 |
thyX | 3067409 | c.537C>T | synonymous_variant | 0.4 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |