Run ID: ERR9285887
Sample name:
Date: 02-04-2023 11:43:50
Number of reads: 810640
Percentage reads mapped: 99.66
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 | 0.98 |
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 |
fgd1 | 490994 | p.Gly71Asp | missense_variant | 0.11 |
fgd1 | 491052 | c.270C>T | synonymous_variant | 0.14 |
mshA | 576285 | p.Val313Ala | missense_variant | 0.12 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.15 |
mshA | 576700 | p.Glu451Asp | missense_variant | 0.15 |
rpoC | 765299 | p.Val644Ile | missense_variant | 0.11 |
rpoC | 766945 | c.3576A>T | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779080 | p.Ser31Gly | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416232 | p.Cys372Gly | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472322 | n.478delA | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473220 | n.1375C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473458 | n.-200G>A | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918190 | p.Arg84Gln | missense_variant | 0.11 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.18 |
PPE35 | 2169690 | p.Gly308Asp | missense_variant | 0.11 |
PPE35 | 2169727 | p.Asn296Asp | missense_variant | 0.1 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.15 |
PPE35 | 2169962 | c.651C>T | synonymous_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.27 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.27 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517960 | c.-154delT | upstream_gene_variant | 0.14 |
folC | 2746646 | p.Gln318Leu | missense_variant | 0.13 |
folC | 2746923 | p.Gly226Ser | missense_variant | 1.0 |
pepQ | 2859839 | p.Val194Leu | missense_variant | 0.12 |
ribD | 2987578 | p.Asp247Gly | missense_variant | 0.1 |
thyA | 3074535 | c.-64C>T | upstream_gene_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 0.97 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.11 |
embC | 4240371 | p.Gly170Glu | missense_variant | 0.12 |
embC | 4240469 | p.Asp203Tyr | missense_variant | 0.12 |
embC | 4242602 | p.Ser914Thr | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242829 | c.-404G>T | upstream_gene_variant | 0.11 |
embA | 4243692 | p.Gly154Ser | missense_variant | 1.0 |
embA | 4245835 | p.Leu868Arg | missense_variant | 0.13 |
embB | 4246904 | p.Val131Met | missense_variant | 1.0 |
aftB | 4267507 | c.1329delC | frameshift_variant | 0.12 |
aftB | 4268196 | p.Val214Ala | missense_variant | 0.1 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 0.11 |
ethA | 4327499 | c.-26C>T | upstream_gene_variant | 0.11 |
ethA | 4328252 | c.-779T>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407740 | p.Pro155Thr | missense_variant | 0.11 |