Run ID: ERR4814963
Sample name:
Date: 01-04-2023 13:35:26
Number of reads: 1545062
Percentage reads mapped: 98.87
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 | 0.25 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5128 | c.-111delA | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7907 | p.Phe202Leu | 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 | 760042 | p.Gly79Val | missense_variant | 0.11 |
rpoB | 760115 | c.309C>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 |
atpE | 1461035 | c.-10G>T | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472912 | n.1067C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472917 | n.1072G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473695 | n.39_40delTC | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473700 | n.43G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473702 | n.45_46insGA | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473717 | n.60G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473718 | n.61G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473744 | n.87T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473748 | n.91A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473751 | n.94C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473753 | n.96A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474202 | n.545T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474249 | n.592G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475504 | n.1847C>A | non_coding_transcript_exon_variant | 0.67 |
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 |
ahpC | 2726274 | p.Ala28Thr | missense_variant | 0.12 |
Rv2752c | 3065207 | p.Thr329Pro | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
ethR | 4326613 | c.-936G>A | upstream_gene_variant | 1.0 |
ethA | 4327389 | p.Thr29Ala | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |