Run ID: ERR11068532
Sample name:
Date: 06-04-2023 16:28:52
Number of reads: 4198084
Percentage reads mapped: 99.42
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
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 |
---|
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 |
mshA | 576116 | p.Ala257Pro | missense_variant | 0.5 |
mshA | 576119 | p.Ala258Pro | missense_variant | 0.4 |
ccsA | 619849 | c.-42G>A | upstream_gene_variant | 0.15 |
ccsA | 619939 | p.Ala17Thr | missense_variant | 0.15 |
ccsA | 620049 | c.159G>A | synonymous_variant | 0.29 |
rpoB | 760106 | c.300G>A | synonymous_variant | 1.0 |
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 |
fbiC | 1304226 | c.1296C>T | synonymous_variant | 0.14 |
fbiC | 1304230 | p.Pro434Ser | missense_variant | 0.12 |
Rv1258c | 1406991 | p.Gly117Asp | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1674381 | c.180G>A | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918108 | p.Asp57Tyr | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2519049 | p.Gly312Asp | missense_variant | 0.13 |
folC | 2746593 | p.Pro336Ser | missense_variant | 1.0 |
pepQ | 2860150 | p.Ala90Val | missense_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339345 | c.228C>G | synonymous_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.33 |
fbiB | 3642711 | c.1177C>T | synonymous_variant | 0.11 |
embC | 4241702 | p.Arg614Cys | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4248329 | p.Met606Leu | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |