Run ID: ERR2987810
Sample name:
Date: 01-04-2023 00:16:29
Number of reads: 307957817
Percentage reads mapped: 98.88
Strain: lineage4.2.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
lineage4.2.1.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
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 |
mmpL5 | 776536 | p.Lys649Gln | missense_variant | 1.0 |
mmpL5 | 777451 | p.Val344Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3064701 | p.Phe497Leu | missense_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3840696 | p.Ala242Val | missense_variant | 0.57 |
ddn | 3987092 | p.Glu83Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408213 | c.-11C>T | upstream_gene_variant | 1.0 |