Run ID: ERR4821192
Sample name:
Date: 01-04-2023 17:06:54
Number of reads: 1326782
Percentage reads mapped: 99.44
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 | 491308 | p.Ala176Ser | missense_variant | 0.5 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576259 | p.Ser304Arg | missense_variant | 0.12 |
ccsA | 620661 | c.771C>A | synonymous_variant | 0.13 |
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 | 1304424 | c.1494C>A | synonymous_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472685 | n.840G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474525 | n.868A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475235 | n.1578C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476634 | n.2977T>C | non_coding_transcript_exon_variant | 0.11 |
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 |
pepQ | 2859786 | c.633G>T | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449042 | p.Val180Gly | missense_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475235 | p.Leu410Gln | missense_variant | 0.15 |
whiB7 | 3568796 | c.-117G>A | upstream_gene_variant | 0.12 |
Rv3236c | 3613232 | c.-116T>C | upstream_gene_variant | 0.13 |
fbiB | 3641915 | c.381C>T | synonymous_variant | 0.25 |
fbiB | 3642062 | p.Tyr176* | stop_gained | 0.14 |
rpoA | 3878129 | c.378delC | frameshift_variant | 0.1 |
clpC1 | 4038281 | c.2424C>T | synonymous_variant | 0.11 |
clpC1 | 4038442 | p.Ala755Thr | missense_variant | 0.12 |
embC | 4242588 | p.Gly909Val | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243746 | p.Gly172Ser | missense_variant | 0.22 |
aftB | 4267095 | p.Pro581Arg | missense_variant | 0.11 |
aftB | 4267544 | c.1293T>C | synonymous_variant | 0.12 |
ubiA | 4269031 | p.Gly268Val | missense_variant | 0.14 |
ubiA | 4269888 | c.-55C>A | upstream_gene_variant | 0.12 |
whiB6 | 4338256 | c.265delG | frameshift_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |