Run ID: ERR2228878
Sample name:
Date: 31-03-2023 16:24:26
Number of reads: 171821
Percentage reads mapped: 99.7
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 8322 | p.Phe341Leu | missense_variant | 0.33 |
ccsA | 619787 | c.-104T>G | upstream_gene_variant | 0.27 |
ccsA | 619958 | p.Val23Gly | missense_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778885 | c.-405T>C | upstream_gene_variant | 0.5 |
mmpR5 | 779066 | p.Tyr26Phe | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800740 | c.-69A>C | upstream_gene_variant | 0.3 |
fbiC | 1303689 | c.759T>A | synonymous_variant | 0.33 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472504 | n.659A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.67 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102653 | p.His130Gln | missense_variant | 0.5 |
PPE35 | 2167891 | p.Gly908Ser | missense_variant | 0.5 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.67 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.67 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290171 | c.-930G>A | upstream_gene_variant | 0.5 |
kasA | 2518163 | p.Thr17Pro | missense_variant | 0.67 |
ahpC | 2726571 | p.Ala127Ser | missense_variant | 0.5 |
folC | 2746745 | p.Val285Asp | missense_variant | 0.5 |
pepQ | 2860351 | p.Leu23Pro | missense_variant | 0.2 |
thyA | 3073757 | p.Phe239Ile | missense_variant | 0.18 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3474106 | p.Met34Leu | missense_variant | 0.2 |
fbiB | 3642436 | p.Gln301Arg | missense_variant | 0.33 |
alr | 3840197 | c.1224T>A | synonymous_variant | 0.22 |
alr | 3841229 | c.192G>T | synonymous_variant | 0.22 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.15 |
ddn | 3986712 | c.-132A>G | upstream_gene_variant | 0.4 |
ddn | 3987022 | p.Arg60Leu | missense_variant | 0.25 |
clpC1 | 4039588 | p.Ser373Ala | missense_variant | 0.5 |
embC | 4240212 | p.Val117Gly | missense_variant | 0.5 |
embC | 4241043 | p.Asn394Thr | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243347 | p.Thr39Pro | missense_variant | 0.2 |
embA | 4243503 | p.Ser91Ala | missense_variant | 0.5 |
embA | 4245640 | p.Asn803Thr | missense_variant | 0.67 |
embA | 4245835 | p.Leu868Gln | missense_variant | 0.25 |
embB | 4246187 | c.-327C>A | upstream_gene_variant | 0.4 |
aftB | 4267842 | p.Asp332Gly | missense_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448498 | c.-5_*1408del | transcript_ablation | 1.0 |