Run ID: SRR20139569
Sample name:
Date: 13-03-2023 09:23:20
Number of reads: 1640717
Percentage reads mapped: 99.62
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 |
lineage4.1.2 | 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 | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
pncA | 2289252 | c.-11A>G | upstream_gene_variant | 1.0 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5740 | c.501G>C | synonymous_variant | 1.0 |
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.18 |
gyrB | 6927 | p.Leu563Trp | missense_variant | 0.14 |
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 | 490751 | c.-32T>G | upstream_gene_variant | 0.16 |
fgd1 | 490756 | c.-27T>G | upstream_gene_variant | 0.25 |
fgd1 | 490780 | c.-3C>A | upstream_gene_variant | 0.15 |
fgd1 | 490803 | c.21T>G | synonymous_variant | 0.18 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576710 | p.Arg455Gly | missense_variant | 0.14 |
mshA | 576718 | c.1371C>G | synonymous_variant | 0.17 |
mshA | 576731 | p.Asp462Ala | missense_variant | 0.21 |
mshA | 576739 | c.1392A>G | synonymous_variant | 0.17 |
mshA | 576740 | p.Ala465Gly | missense_variant | 0.16 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.18 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.27 |
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 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.19 |
fbiC | 1303038 | c.108T>G | synonymous_variant | 0.17 |
fbiC | 1303055 | p.Asp42Gly | missense_variant | 0.21 |
fbiC | 1304159 | p.Val410Gly | missense_variant | 0.27 |
fbiC | 1304166 | c.1236A>G | synonymous_variant | 0.16 |
fbiC | 1304174 | p.Val415Gly | missense_variant | 0.18 |
Rv1258c | 1407055 | p.Tyr96Asp | missense_variant | 0.18 |
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 | 0.16 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2714549 | p.Met262Leu | missense_variant | 0.16 |
eis | 2714552 | p.Ser261Pro | missense_variant | 0.14 |
eis | 2715468 | c.-136C>T | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val50Gly | missense_variant | 0.22 |
ahpC | 2726344 | c.153C>T | synonymous_variant | 0.17 |
ahpC | 2726350 | p.Trp53Leu | missense_variant | 0.38 |
thyA | 3074608 | c.-137A>G | upstream_gene_variant | 0.17 |
thyA | 3074646 | c.-177T>G | upstream_gene_variant | 0.21 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-10_-9insA | upstream_gene_variant | 1.0 |
embC | 4240188 | p.Val109Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249305 | p.Asn931Thr | missense_variant | 0.24 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.22 |
ethA | 4326060 | p.Lys472* | stop_gained | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407983 | c.217delG | frameshift_variant | 1.0 |