Run ID: ERR181733
Sample name:
Date: 31-03-2023 15:17:55
Number of reads: 4468874
Percentage reads mapped: 86.63
Strain: lineage4.3.4.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 0.99 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
lineage4.3.4.2.1 | Euro-American (LAM) | LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6140 | p.Val301Leu | missense_variant | 0.99 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472128 | n.283G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472129 | n.284G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472139 | n.294C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472146 | n.301G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472181 | n.336G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472574 | n.729T>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472592 | n.747C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472698 | n.853A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472701 | n.856T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472719 | n.874G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472733 | n.888G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472742 | n.897C>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476381 | n.2724G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476427 | n.2770G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.19 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.23 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.27 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.31 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 0.99 |
alr | 3840719 | c.702A>G | synonymous_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.21 |
embC | 4239842 | c.-21C>A | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338548 | c.-27G>C | upstream_gene_variant | 0.99 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |