Run ID: ERR495087
Sample name:
Date: 01-04-2023 21:37:43
Number of reads: 581810
Percentage reads mapped: 99.71
Strain:
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 | 491308 | p.Ala176Thr | missense_variant | 0.25 |
fgd1 | 491312 | p.Gly177Ala | missense_variant | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.75 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620751 | p.Trp287Cys | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765189 | p.Pro607Gln | missense_variant | 0.25 |
rpoC | 767041 | c.3672G>A | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775675 | p.Trp936Arg | missense_variant | 0.22 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416372 | p.Ser326Gly | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101697 | p.Ala449Val | missense_variant | 0.13 |
kasA | 2518417 | c.303G>T | synonymous_variant | 0.25 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
Rv2752c | 3065504 | p.Asp230Tyr | missense_variant | 0.5 |
Rv3083 | 3448985 | p.Gly161Asp | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475093 | p.Gly363Trp | missense_variant | 0.18 |
embC | 4239736 | c.-127C>A | upstream_gene_variant | 0.13 |
embC | 4241375 | p.Ala505Thr | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4246069 | p.Pro946Gln | missense_variant | 0.18 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethR | 4327643 | p.Thr32Ile | missense_variant | 0.4 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |