Run ID: SRR023452
Sample name:
Date: 02-04-2023 14:12:05
Number of reads: 5286126
Percentage reads mapped: 97.15
Strain: lineage4.1.2.1
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 |
lineage4.1.2 | 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 |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
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 | 491414 | p.Val211Gly | missense_variant | 0.37 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.94 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.96 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.96 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777502 | p.Thr327Pro | missense_variant | 0.23 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304071 | p.Thr381Pro | missense_variant | 0.44 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673449 | p.Thr4Pro | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155375 | p.Val246Gly | missense_variant | 0.2 |
katG | 2155726 | p.Phe129Ser | missense_variant | 1.0 |
PPE35 | 2170357 | p.Ala86Ser | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.99 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518144 | c.30T>G | synonymous_variant | 0.24 |
kasA | 2518163 | p.Thr17Pro | missense_variant | 0.15 |
eis | 2715098 | p.Thr79Pro | missense_variant | 0.18 |
pepQ | 2860126 | p.Glu98Gly | missense_variant | 0.15 |
thyA | 3074654 | c.-183T>G | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612422 | p.Val232Gly | missense_variant | 0.18 |
rpoA | 3877949 | p.Thr187Ala | missense_variant | 1.0 |
rpoA | 3878647 | c.-140delG | upstream_gene_variant | 0.12 |
ddn | 3986929 | p.Tyr29Ser | missense_variant | 0.14 |
embC | 4240619 | p.Thr253Pro | missense_variant | 0.14 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.36 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4247822 | p.Thr437Pro | missense_variant | 0.22 |
embB | 4247868 | p.Val452Ala | missense_variant | 0.33 |
embB | 4248614 | p.Ala701Thr | missense_variant | 1.0 |
ubiA | 4269317 | p.Ser173Ala | missense_variant | 1.0 |