Run ID: ERR5865200
Sample name:
Date: 01-04-2023 23:51:42
Number of reads: 1131200
Percentage reads mapped: 99.73
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 | 761086 | p.Thr427Ser | missense_variant | 1.0 | rifampicin |
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288778 | p.Val155Ala | missense_variant | 1.0 | pyrazinamide |
eis | 2715346 | c.-14C>T | upstream_gene_variant | 1.0 | kanamycin, amikacin |
embB | 4247730 | p.Gly406Asp | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6162 | c.924delC | frameshift_variant | 0.25 |
gyrB | 6268 | c.1029C>A | synonymous_variant | 0.11 |
gyrB | 6297 | p.Gly353Val | missense_variant | 0.1 |
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 | 576751 | p.Lys468Asn | missense_variant | 0.2 |
rpoC | 762611 | c.-759C>T | upstream_gene_variant | 0.2 |
rpoB | 763059 | p.Ile1085Phe | missense_variant | 0.17 |
rpoC | 763728 | p.Leu120Pro | missense_variant | 0.13 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303095 | c.165G>A | synonymous_variant | 0.94 |
fbiC | 1305183 | p.Leu751Phe | missense_variant | 0.12 |
atpE | 1461231 | p.Ala63Ser | missense_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673400 | c.-40C>T | upstream_gene_variant | 0.11 |
rpsA | 1833764 | p.Asp75Asn | missense_variant | 0.13 |
rpsA | 1834025 | p.Gln162Lys | missense_variant | 0.11 |
rpsA | 1834088 | p.Val183Met | missense_variant | 1.0 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
rpsA | 1834942 | p.Asp467Glu | missense_variant | 0.18 |
tlyA | 1917785 | c.-154delG | upstream_gene_variant | 0.12 |
tlyA | 1917795 | c.-145G>C | upstream_gene_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102098 | c.945G>A | synonymous_variant | 1.0 |
katG | 2156196 | c.-85C>T | upstream_gene_variant | 1.0 |
PPE35 | 2167837 | p.Gly926Arg | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290044 | c.-803G>T | upstream_gene_variant | 0.11 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.17 |
eis | 2714319 | c.1014G>A | synonymous_variant | 0.15 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.18 |
folC | 2746340 | p.Ala420Val | missense_variant | 1.0 |
folC | 2746658 | p.Gly314Val | missense_variant | 0.22 |
folC | 2747135 | p.Leu155His | missense_variant | 0.15 |
Rv2752c | 3064916 | p.Gly426Cys | missense_variant | 0.14 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
thyA | 3074036 | p.Cys146Arg | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612046 | c.1071G>A | synonymous_variant | 0.11 |
Rv3236c | 3612839 | p.Ala93Val | missense_variant | 0.17 |
rpoA | 3878367 | c.141C>T | synonymous_variant | 0.15 |
rpoA | 3878487 | c.21C>A | synonymous_variant | 0.13 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.67 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038968 | c.1737G>A | synonymous_variant | 1.0 |
clpC1 | 4040339 | c.365delA | frameshift_variant | 0.12 |
panD | 4044373 | c.-92C>A | upstream_gene_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4268311 | p.Ala176Thr | missense_variant | 0.11 |
ethA | 4326266 | p.Cys403Phe | missense_variant | 1.0 |
ethA | 4326537 | p.Val313Leu | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407952 | p.Pro84Arg | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |