Run ID: SRR6982085
Sample name:
Date: 04-04-2023 18:26:51
Number of reads: 587784
Percentage reads mapped: 99.1
Strain: lineage4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 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 |
ccsA | 619940 | p.Ala17Val | missense_variant | 0.12 |
ccsA | 620319 | c.429C>T | synonymous_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779125 | p.Cys46Arg | missense_variant | 0.12 |
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 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714422 | p.Ala304Val | missense_variant | 1.0 |
pepQ | 2859482 | p.Ala313Thr | missense_variant | 0.11 |
pepQ | 2860235 | p.Thr62Ala | missense_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339645 | c.528C>G | synonymous_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640651 | p.Ala37Pro | missense_variant | 0.12 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 1.0 |
alr | 3840365 | c.1056C>T | synonymous_variant | 0.12 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.94 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243054 | c.-179G>A | upstream_gene_variant | 0.12 |
embB | 4247484 | p.Gly324Asp | missense_variant | 0.11 |
embB | 4247670 | p.Ala386Glu | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 0.85 |
aftB | 4267091 | c.1746C>A | synonymous_variant | 0.13 |
aftB | 4267351 | p.Met496Leu | missense_variant | 0.12 |
aftB | 4267603 | p.Arg412Gly | missense_variant | 0.13 |
aftB | 4268620 | p.Val73Leu | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |