Run ID: ERR4818539
Sample name:
Date: 01-04-2023 15:36:58
Number of reads: 711166
Percentage reads mapped: 99.45
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 | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5597 | p.Leu120Val | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7930 | p.Ala210Val | missense_variant | 1.0 |
gyrA | 8629 | p.Leu443Pro | missense_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491523 | c.745delT | frameshift_variant | 0.18 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 759620 | c.-187A>C | upstream_gene_variant | 0.33 |
rpoB | 759678 | c.-129T>C | upstream_gene_variant | 0.12 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 764484 | p.Arg372Gln | missense_variant | 0.14 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766817 | p.His1150Asn | missense_variant | 0.27 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779407 | c.421dupG | frameshift_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167859 | c.2754T>G | synonymous_variant | 0.38 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.13 |
PPE35 | 2169272 | c.1341C>A | synonymous_variant | 0.13 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.14 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.23 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518274 | p.Trp54Arg | missense_variant | 0.15 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.29 |
folC | 2746495 | p.His368Gln | missense_variant | 0.22 |
thyA | 3074660 | c.-189C>A | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640415 | c.-128T>C | upstream_gene_variant | 1.0 |
embC | 4240180 | c.318G>A | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245143 | c.1911C>A | synonymous_variant | 0.1 |
embB | 4249330 | p.Met939Ile | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |