Run ID: ERR2652980
Sample name:
Date: 31-03-2023 22:25:51
Number of reads: 1062253
Percentage reads mapped: 99.37
Strain: lineage4.4.1.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7922 | p.Asn207Lys | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303151 | p.Gly74Ala | missense_variant | 0.2 |
fbiC | 1303393 | p.Trp155Arg | missense_variant | 1.0 |
fbiC | 1304052 | c.1122G>A | synonymous_variant | 0.12 |
Rv1258c | 1407075 | p.Val89Gly | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 0.99 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.4 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715545 | c.-213C>T | upstream_gene_variant | 0.29 |
folC | 2746590 | p.Gly337Ser | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339565 | p.Val150Leu | missense_variant | 0.12 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
rpoA | 3878639 | c.-132C>G | upstream_gene_variant | 0.12 |
embC | 4240460 | p.Val200Met | missense_variant | 0.14 |
embC | 4242188 | p.Ala776Thr | missense_variant | 0.12 |
embC | 4242227 | p.Gly789Ser | missense_variant | 0.12 |
embA | 4242328 | c.-905C>T | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242676 | c.-557C>T | upstream_gene_variant | 0.12 |
embC | 4242699 | p.Val946Ala | missense_variant | 0.11 |
embA | 4243482 | p.Ala84Thr | missense_variant | 0.22 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.1 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.11 |
aftB | 4267585 | p.Thr418Pro | missense_variant | 0.11 |
aftB | 4267593 | p.Ala415Val | missense_variant | 0.12 |
aftB | 4268358 | p.Gln160Arg | missense_variant | 0.1 |
whiB6 | 4338228 | c.294G>A | synonymous_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |