Run ID: ERR025413
Sample name:
Date: 31-03-2023 08:15:40
Number of reads: 744474
Percentage reads mapped: 99.31
Strain: lineage4.3.2;lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.07 |
lineage4.1 | Euro-American | T;X;H | None | 0.85 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 0.12 |
lineage4.1.2 | Euro-American | T;H | None | 0.83 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.71 |
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 | 491591 | p.Lys270Met | missense_variant | 0.83 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.75 |
ccsA | 620407 | p.Pro173Ala | missense_variant | 0.27 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.84 |
rpoC | 764365 | c.996C>G | synonymous_variant | 0.38 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.8 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779048 | p.Val20Ala | missense_variant | 0.24 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1461019 | c.-26C>A | upstream_gene_variant | 0.17 |
atpE | 1461179 | c.135G>T | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475363 | n.1706C>A | non_coding_transcript_exon_variant | 0.32 |
rpsA | 1834631 | p.Gln364Lys | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102540 | p.Ala168Gly | missense_variant | 0.2 |
PPE35 | 2169783 | p.Thr277Lys | missense_variant | 0.42 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.17 |
Rv1979c | 2223057 | c.108A>G | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.8 |
Rv2752c | 3064552 | p.Arg547Pro | missense_variant | 0.24 |
thyA | 3074657 | c.-186C>G | upstream_gene_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474400 | p.Tyr132Asp | missense_variant | 0.2 |
fbiB | 3641955 | p.Gly141Arg | missense_variant | 0.25 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.25 |
clpC1 | 4039932 | p.Gly258Val | missense_variant | 0.36 |
embC | 4241429 | p.Phe523Val | missense_variant | 0.22 |
embC | 4242476 | p.Pro872Ala | missense_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.89 |
embA | 4242883 | c.-350C>G | upstream_gene_variant | 0.17 |
embA | 4244375 | c.1143C>G | synonymous_variant | 0.29 |
embA | 4244844 | p.Arg538Cys | missense_variant | 0.18 |
embA | 4246218 | p.His996Tyr | missense_variant | 0.13 |
aftB | 4268812 | p.Ser9Ala | missense_variant | 0.23 |
ubiA | 4269864 | c.-31C>G | upstream_gene_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407644 | p.Arg187Trp | missense_variant | 0.38 |