Run ID: ERR4820135
Sample name:
Date: 01-04-2023 16:30:38
Number of reads: 4889029
Percentage reads mapped: 99.14
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.43 | streptomycin |
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 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 764095 | c.726C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_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 | 1472117 | n.272A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472543 | n.699_700delCA | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476620 | n.2963A>G | non_coding_transcript_exon_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | 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 |
rpoA | 3878638 | c.-131C>T | upstream_gene_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |