Run ID: ERR10748234
Sample name:
Date: 31-03-2023 10:48:22
Number of reads: 689304
Percentage reads mapped: 99.76
Strain: lineage4.1.1.2;lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.27 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.73 |
lineage4.1 | Euro-American | T;X;H | None | 0.72 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.31 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.36 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 0.77 |
lineage4.1.1.2 | Euro-American (X-type) | X1 | None | 0.7 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.39 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.3 | isoniazid |
pncA | 2288930 | p.Ser104Arg | missense_variant | 0.32 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 0.33 | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.34 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.31 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.35 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.57 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.12 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.16 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.41 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.27 |
katG | 2155296 | c.816C>T | synonymous_variant | 0.81 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.31 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449787 | c.1284C>T | synonymous_variant | 0.76 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.26 |
alr | 3840597 | p.Met275Thr | missense_variant | 0.32 |
clpC1 | 4039676 | c.1029G>A | synonymous_variant | 0.35 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.83 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.24 |
embA | 4243833 | p.Ala201Thr | missense_variant | 0.71 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.25 |
embB | 4246930 | p.Gln139His | missense_variant | 0.72 |
embB | 4249408 | c.2895G>A | synonymous_variant | 0.58 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.26 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.32 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.11 |