Run ID: ERR4827467
Sample name:
Date: 01-04-2023 18:04:26
Number of reads: 794283
Percentage reads mapped: 98.94
Strain: lineage4.5
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 |
lineage4.5 | Euro-American | H;T | RD122 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761140 | p.His445Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Ile | missense_variant | 1.0 | isoniazid |
embB | 4247574 | p.Asp354Ala | missense_variant | 0.96 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7892 | c.591G>A | synonymous_variant | 0.95 |
gyrA | 8500 | p.Ala400Gly | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
ccsA | 620029 | c.139C>T | synonymous_variant | 1.0 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406101 | p.Pro414Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.12 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168225 | c.2388C>A | synonymous_variant | 0.22 |
PPE35 | 2169049 | p.Ile522Phe | missense_variant | 0.29 |
PPE35 | 2169082 | p.Leu511Val | missense_variant | 0.25 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.59 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.61 |
PPE35 | 2170454 | c.159C>G | synonymous_variant | 0.12 |
PPE35 | 2170457 | c.156G>C | synonymous_variant | 0.12 |
PPE35 | 2170521 | p.Trp31* | stop_gained | 0.94 |
PPE35 | 2170568 | p.Ile15Met | missense_variant | 1.0 |
Rv1979c | 2223189 | c.-25T>A | upstream_gene_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289731 | c.-490A>T | upstream_gene_variant | 0.12 |
pncA | 2289737 | c.-496A>G | upstream_gene_variant | 0.12 |
pncA | 2289740 | c.-499T>C | upstream_gene_variant | 0.12 |
pncA | 2289903 | c.-662C>T | upstream_gene_variant | 0.13 |
ahpC | 2726285 | c.93C>T | synonymous_variant | 0.12 |
folC | 2746245 | p.Ala452Thr | missense_variant | 0.13 |
folC | 2746572 | p.Arg343Cys | missense_variant | 0.22 |
folC | 2746616 | p.Ala328Asp | missense_variant | 0.18 |
thyX | 3068028 | c.-83G>T | upstream_gene_variant | 0.13 |
thyX | 3068127 | c.-182G>C | upstream_gene_variant | 0.14 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612666 | p.Val151Met | missense_variant | 1.0 |
Rv3236c | 3612719 | p.Ile133Thr | missense_variant | 0.17 |
fbiB | 3642470 | c.936G>A | synonymous_variant | 0.12 |
clpC1 | 4038318 | p.Pro796Leu | missense_variant | 1.0 |
clpC1 | 4038483 | p.Gln741Arg | missense_variant | 0.14 |
clpC1 | 4039425 | p.Lys427Met | missense_variant | 0.11 |
embC | 4240291 | c.429G>A | synonymous_variant | 0.14 |
embC | 4240608 | p.His249Arg | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245708 | c.2477delC | frameshift_variant | 0.2 |
embB | 4245845 | c.-669T>A | upstream_gene_variant | 0.2 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.18 |
embB | 4249188 | p.Tyr892Cys | missense_variant | 0.13 |
aftB | 4268021 | c.816G>T | synonymous_variant | 0.2 |
aftB | 4268519 | p.Tyr106* | stop_gained | 0.2 |
ubiA | 4269879 | c.-46C>T | upstream_gene_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407727 | p.Met159Pro | missense_variant | 1.0 |
gid | 4407818 | p.Gly129Cys | missense_variant | 1.0 |