Run ID: ERR4822235
Sample name:
Date: 01-04-2023 17:42:54
Number of reads: 1135944
Percentage reads mapped: 99.46
Strain: lineage2.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.96 |
mshA | 576488 | p.Val381Gln | missense_variant | 0.18 |
ccsA | 620014 | p.Arg42Ser | missense_variant | 0.25 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473159 | n.1314C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473889 | n.232G>A | non_coding_transcript_exon_variant | 0.11 |
inhA | 1673643 | c.-559C>T | upstream_gene_variant | 0.13 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167929 | p.Ser895Leu | missense_variant | 0.13 |
PPE35 | 2170355 | c.258G>A | synonymous_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518863 | p.Thr250Lys | missense_variant | 0.17 |
eis | 2714918 | p.Glu139Gln | missense_variant | 0.12 |
ald | 3086747 | c.-73A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339366 | c.249G>A | synonymous_variant | 0.15 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568408 | p.Val91Asp | missense_variant | 0.14 |
Rv3236c | 3612378 | p.Val247Leu | missense_variant | 0.14 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878531 | c.-24A>G | upstream_gene_variant | 0.33 |
clpC1 | 4039638 | p.Ile356Thr | missense_variant | 0.32 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243553 | c.321C>A | synonymous_variant | 0.2 |
embA | 4244805 | p.Leu525Met | missense_variant | 0.12 |
embB | 4247066 | p.Ile185Val | missense_variant | 0.18 |
embB | 4247915 | p.Arg468Gly | missense_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408334 | c.-132G>T | upstream_gene_variant | 0.11 |
gid | 4408472 | c.-270C>T | upstream_gene_variant | 0.17 |