Run ID: ERR11068720
Sample name:
Date: 06-04-2023 23:21:45
Number of reads: 3513913
Percentage reads mapped: 99.57
Strain: lineage4.4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | 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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576044 | p.Ala233Thr | missense_variant | 0.12 |
mshA | 576119 | p.Ala258Pro | missense_variant | 0.25 |
mshA | 576649 | c.1302C>T | synonymous_variant | 0.17 |
mshA | 576687 | p.Glu447Gly | missense_variant | 0.25 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918572 | c.633C>T | synonymous_variant | 0.11 |
ndh | 2102342 | p.Ala234Val | missense_variant | 0.11 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
katG | 2155069 | p.Ala348Gly | missense_variant | 1.0 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746758 | p.Gly281Ser | missense_variant | 1.0 |
ribD | 2987298 | p.Gln154Glu | missense_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
alr | 3841117 | p.Ala102Thr | missense_variant | 0.12 |
alr | 3841133 | c.288G>A | synonymous_variant | 0.1 |
clpC1 | 4038217 | p.Pro830Ser | missense_variant | 0.11 |
embC | 4242479 | p.Thr873Ser | missense_variant | 0.11 |
embC | 4242530 | p.Arg890* | stop_gained | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247915 | p.Arg468Cys | missense_variant | 0.25 |
whiB6 | 4338547 | c.-26A>G | upstream_gene_variant | 0.9 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |