Run ID: ERR11049474
Sample name:
Date: 01-04-2023 05:17:38
Number of reads: 6396738
Percentage reads mapped: 99.57
Strain: lineage4.5
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.5 | Euro-American | H;T | RD122 | 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 | 7892 | c.591G>A | synonymous_variant | 1.0 |
gyrA | 8155 | p.Thr285Ile | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.19 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.3 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.29 |
ccsA | 620029 | c.139C>T | synonymous_variant | 1.0 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.21 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.19 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406101 | p.Pro414Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.35 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.3 |
PPE35 | 2170568 | p.Ile15Met | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.27 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.18 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.45 |
fbiD | 3339749 | p.Val211Gly | missense_variant | 0.3 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568425 | c.255T>C | synonymous_variant | 0.27 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.47 |
Rv3236c | 3612267 | p.Pro284Ala | missense_variant | 1.0 |
rpoA | 3878575 | c.-68C>T | upstream_gene_variant | 1.0 |
rpoA | 3878597 | c.-90G>C | upstream_gene_variant | 0.26 |
rpoA | 3878609 | c.-102T>G | upstream_gene_variant | 0.4 |
rpoA | 3878613 | c.-106A>C | upstream_gene_variant | 0.6 |
rpoA | 3878618 | c.-111A>C | upstream_gene_variant | 0.29 |
rpoA | 3878639 | c.-132C>G | upstream_gene_variant | 0.12 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.49 |
clpC1 | 4038318 | p.Pro796Leu | missense_variant | 1.0 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.35 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.27 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.15 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.3 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.32 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.22 |
whiB6 | 4338205 | p.Val106Gly | missense_variant | 0.21 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |