Run ID: SRR10808501
Sample name:
Date: 02-04-2023 18:56:34
Number of reads: 868969
Percentage reads mapped: 99.74
Strain: lineage2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.1 | East-Asian (non-Beijing) | None | None | 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 | 7795 | p.Val165Ala | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.4 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.96 |
rpoC | 765121 | c.1752G>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304443 | p.Ala505Thr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476012 | n.2355T>C | non_coding_transcript_exon_variant | 0.1 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.96 |
rpsA | 1834588 | c.1047C>T | synonymous_variant | 1.0 |
rpsA | 1834914 | p.Lys458Arg | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102835 | p.Pro70Ser | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155506 | c.606C>A | synonymous_variant | 1.0 |
katG | 2156335 | c.-224C>T | upstream_gene_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.5 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.54 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747463 | p.Ser46Cys | missense_variant | 0.11 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4040841 | c.-138delG | upstream_gene_variant | 1.0 |
embC | 4241063 | p.Ile401Phe | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4245716 | c.-798G>A | upstream_gene_variant | 0.17 |
embB | 4246088 | c.-426A>G | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.27 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.3 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.43 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.43 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.33 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.29 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4269471 | c.-635C>G | upstream_gene_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |