Run ID: ERR4828888
Sample name:
Date: 01-04-2023 19:09:05
Number of reads: 1013852
Percentage reads mapped: 99.69
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 | 576089 | p.Ala254Gly | missense_variant | 0.27 |
ccsA | 620250 | c.360C>G | 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 |
mmpL5 | 775973 | c.2508G>A | synonymous_variant | 0.12 |
mmpR5 | 778403 | c.-587T>C | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406593 | p.Tyr250Asn | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472104 | n.260delT | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476495 | n.2838A>G | non_coding_transcript_exon_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102214 | p.Ser277Thr | missense_variant | 0.11 |
PPE35 | 2167800 | p.Gly938Val | missense_variant | 0.15 |
PPE35 | 2168512 | p.Gly701Ser | missense_variant | 0.2 |
PPE35 | 2168946 | p.Pro556Leu | missense_variant | 1.0 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.2 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
Rv2752c | 3064655 | p.Ala513Ser | missense_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087817 | p.Cys333Phe | missense_variant | 0.21 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568427 | p.Arg85Gly | missense_variant | 0.25 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.25 |
whiB7 | 3568586 | p.Thr32Ala | missense_variant | 0.11 |
whiB7 | 3568588 | p.Asp31Val | missense_variant | 0.11 |
rpoA | 3878583 | c.-76C>A | upstream_gene_variant | 1.0 |
clpC1 | 4038740 | c.1965G>T | synonymous_variant | 0.14 |
clpC1 | 4039829 | p.Leu292Ile | missense_variant | 0.12 |
clpC1 | 4040471 | c.234T>A | synonymous_variant | 0.12 |
embC | 4239713 | c.-150G>A | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
ethA | 4327543 | c.-70C>T | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |