Run ID: ERR4797086
Sample name:
Date: 01-04-2023 07:21:07
Number of reads: 4343046
Percentage reads mapped: 99.82
Strain: lineage4.4.1.2
Drug-resistance: Other
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 | 0.99 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 0.99 |
lineage4.4.1.2 | Euro-American | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
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 |
fgd1 | 490756 | c.-27T>G | upstream_gene_variant | 0.18 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.3 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.29 |
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 | 1471793 | n.-53G>T | upstream_gene_variant | 0.33 |
rrs | 1471805 | n.-41C>A | upstream_gene_variant | 0.38 |
rrl | 1473619 | n.-39G>A | upstream_gene_variant | 0.11 |
rrl | 1473906 | n.249G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474191 | n.534C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475660 | n.2003A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475950 | n.2293C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476311 | n.2654G>A | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2167770 | p.Ser948Ile | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289805 | c.-564C>T | upstream_gene_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.3 |
pepQ | 2860213 | p.Pro69Leu | missense_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 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.23 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.18 |
embC | 4240479 | p.Gly206Glu | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247024 | p.Pro171Ala | missense_variant | 0.17 |
embB | 4248324 | p.Ala604Gly | missense_variant | 0.34 |
embB | 4249012 | c.2499G>A | synonymous_variant | 1.0 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.24 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |