Run ID: ERR4816869
Sample name:
Date: 01-04-2023 14:40:43
Number of reads: 2838768
Percentage reads mapped: 98.58
Strain: lineage4.3.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.3 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5078 | c.-162_-161insG | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | 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 |
fbiC | 1303095 | c.165G>A | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.26 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 0.96 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
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 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |