Run ID: ERR4812795
Sample name:
Date: 01-04-2023 12:20:36
Number of reads: 507210
Percentage reads mapped: 99.1
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 |
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 |
---|---|---|---|---|
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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576612 | p.Ala422Glu | missense_variant | 0.5 |
rpoB | 761104 | p.Phe433Ser | missense_variant | 0.14 |
rpoB | 763290 | p.Arg1162Ser | missense_variant | 0.14 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.14 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 779680 | c.-775G>T | upstream_gene_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834985 | c.1445dupG | frameshift_variant&stop_lost&splice_region_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168998 | p.Ile539Val | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
pepQ | 2860396 | p.Asp8Gly | missense_variant | 0.13 |
thyX | 3067340 | p.Glu202Asp | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074328 | p.Lys48Asn | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087533 | c.714C>A | synonymous_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
panD | 4044172 | c.107_109dupCCG | conservative_inframe_insertion | 0.15 |
embC | 4240681 | c.819G>T | synonymous_variant | 0.33 |
embC | 4241366 | p.Leu502Ile | missense_variant | 0.4 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
ubiA | 4269754 | p.Val27Ala | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |