Run ID: ERR234571
Sample name:
Date: 31-03-2023 18:05:52
Number of reads: 3549331
Percentage reads mapped: 99.67
Strain: lineage4.4.1.1;lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.18 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.83 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.16 |
lineage4.4 | Euro-American | S;T | None | 0.77 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.16 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 0.75 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 0.73 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 762089 | p.Glu761Asp | missense_variant | 0.15 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.16 | isoniazid |
embB | 4247574 | p.Asp354Ala | missense_variant | 0.11 | 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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.13 |
ccsA | 619876 | c.-15C>T | upstream_gene_variant | 0.65 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.33 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.19 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.22 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.23 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.17 |
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 | 0.26 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 0.79 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.18 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.15 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 0.83 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.26 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 0.67 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 0.82 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.24 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.31 |
embC | 4242425 | p.Arg855Gly | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.3 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.23 |
ethA | 4328376 | c.-903G>C | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.14 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.21 |