Run ID: ERR11050530
Sample name:
Date: 03-04-2023 09:10:04
Number of reads: 6354007
Percentage reads mapped: 99.48
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 | 0.99 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.24 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.3 |
mshA | 576613 | c.1266A>C | synonymous_variant | 0.3 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.3 |
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 | 777883 | p.Gly200Arg | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.3 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168981 | c.1632A>G | synonymous_variant | 1.0 |
PPE35 | 2168985 | p.Thr543Met | missense_variant | 1.0 |
PPE35 | 2168987 | p.Thr542Ala | missense_variant | 1.0 |
PPE35 | 2168990 | c.1623T>G | synonymous_variant | 1.0 |
PPE35 | 2169029 | p.Asp528Asn | missense_variant | 0.12 |
PPE35 | 2169041 | c.1572G>A | synonymous_variant | 0.79 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289873 | c.-640_-633delGTGCCGCC | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.24 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.79 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.23 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878589 | c.-82A>T | upstream_gene_variant | 0.14 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.22 |
rpoA | 3878613 | c.-106A>C | upstream_gene_variant | 0.29 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.58 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.2 |
embB | 4246659 | p.Val49Ala | missense_variant | 1.0 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.2 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |