Run ID: ERR4813072
Sample name:
Date: 01-04-2023 12:31:18
Number of reads: 682123
Percentage reads mapped: 99.53
Strain: lineage4.3.3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
tlyA | 1918634 | p.Gly232Asp | missense_variant | 1.0 | capreomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289213 | p.Gln10Arg | missense_variant | 1.0 | pyrazinamide |
embB | 4247469 | p.Tyr319Ser | missense_variant | 1.0 | ethambutol |
gid | 4407952 | p.Pro84Leu | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5366 | p.His43Tyr | missense_variant | 0.11 |
gyrB | 6477 | p.Ser413Leu | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8969 | c.1668G>T | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 619833 | c.-58T>C | upstream_gene_variant | 0.25 |
rpoB | 759647 | c.-160T>C | upstream_gene_variant | 0.12 |
rpoB | 761814 | p.Ala670Thr | missense_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765450 | p.Ala694Val | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801280 | p.Ala158Ser | missense_variant | 0.12 |
embR | 1417532 | c.-185T>C | upstream_gene_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673288 | c.-152G>T | upstream_gene_variant | 0.11 |
fabG1 | 1673638 | p.Ala67Ser | missense_variant | 0.14 |
inhA | 1673658 | c.-544G>A | upstream_gene_variant | 0.14 |
inhA | 1674550 | p.Ser117Pro | missense_variant | 0.2 |
rpsA | 1834985 | c.1445dupG | frameshift_variant&stop_lost&splice_region_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918361 | p.Pro141Gln | missense_variant | 0.12 |
ndh | 2102776 | c.267C>G | synonymous_variant | 0.12 |
PPE35 | 2167684 | p.Leu977Met | missense_variant | 0.11 |
PPE35 | 2168998 | p.Ile539Val | missense_variant | 1.0 |
PPE35 | 2169973 | p.Gly214Cys | missense_variant | 0.12 |
PPE35 | 2170629 | c.-17C>A | upstream_gene_variant | 0.11 |
Rv1979c | 2222240 | p.Leu309Met | missense_variant | 0.29 |
Rv1979c | 2222268 | c.897C>A | synonymous_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289412 | c.-171C>A | upstream_gene_variant | 0.12 |
kasA | 2518443 | p.Val110Ala | missense_variant | 0.12 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
kasA | 2519291 | p.Asp393Asn | missense_variant | 0.17 |
eis | 2714545 | p.Glu263Gly | missense_variant | 0.14 |
folC | 2747518 | c.81G>T | synonymous_variant | 0.2 |
ribD | 2987487 | p.Pro217Thr | missense_variant | 0.11 |
ribD | 2987498 | c.660C>A | synonymous_variant | 0.13 |
thyX | 3067611 | p.Lys112Arg | missense_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339653 | c.537delA | frameshift_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.96 |
Rv3236c | 3612967 | c.150G>A | synonymous_variant | 0.18 |
fbiB | 3642807 | p.Ala425Thr | missense_variant | 0.12 |
ddn | 3986798 | c.-46G>T | upstream_gene_variant | 0.11 |
ddn | 3986801 | c.-43G>T | upstream_gene_variant | 0.11 |
ddn | 3987022 | p.Arg60Gln | missense_variant | 0.15 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038397 | p.Ala770Thr | missense_variant | 0.11 |
embC | 4240518 | p.Asp219Val | missense_variant | 0.15 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245907 | p.Leu892Pro | missense_variant | 0.4 |
aftB | 4269003 | c.-167C>A | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407740 | p.Pro155Thr | missense_variant | 0.25 |
gid | 4407934 | p.Leu90His | missense_variant | 0.2 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |