Run ID: SRR2101525
Sample name:
Date: 03-04-2023 23:46:23
Number of reads: 715812
Percentage reads mapped: 99.56
Strain: lineage4.1.1.3
Drug-resistance: RR-TB
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 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 0.11 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6525 | p.Arg429Leu | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765762 | p.Pro798Arg | missense_variant | 0.1 |
rpoC | 766844 | p.Arg1159Ser | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776107 | p.Leu792Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302793 | c.-138A>G | upstream_gene_variant | 0.1 |
fbiC | 1304190 | c.1260G>A | synonymous_variant | 0.17 |
Rv1258c | 1406887 | p.Leu152Met | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.21 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746860 | p.Ala247Ser | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475004 | p.Pro333Gln | missense_variant | 0.14 |
fprA | 3475132 | p.Gln376Lys | missense_variant | 0.15 |
Rv3236c | 3612401 | p.Ser239* | stop_gained | 0.13 |
Rv3236c | 3612882 | p.Ala79Ser | missense_variant | 0.13 |
embC | 4240688 | p.Leu276Met | missense_variant | 0.13 |
embC | 4242197 | p.Ala779Ser | missense_variant | 0.12 |
embC | 4242492 | p.Arg877Leu | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244528 | c.1296G>C | synonymous_variant | 0.11 |
embA | 4244859 | p.Gly543Trp | missense_variant | 0.13 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.15 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.15 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.14 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.14 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.13 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.12 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
embB | 4249479 | p.Ala989Glu | missense_variant | 0.13 |
aftB | 4267795 | p.Ala348Ser | missense_variant | 0.11 |
aftB | 4268662 | p.Thr59Ala | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |