Run ID: SRR7645856
Sample name:
Date: 04-04-2023 19:55:13
Number of reads: 3774774
Percentage reads mapped: 67.21
Strain: lineage4.4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302887 | c.-44T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472108 | n.263C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472129 | n.284G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472135 | n.290C>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472153 | n.308G>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476588 | n.2931A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476595 | n.2938C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476602 | n.2945G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476611 | n.2954T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476621 | n.2964C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407965 | p.Ala80Thr | missense_variant | 1.0 |