Run ID: ERR11050795
Sample name:
Date: 03-04-2023 21:24:48
Number of reads: 2901125
Percentage reads mapped: 99.68
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 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 |
fgd1 | 490756 | c.-27T>G | upstream_gene_variant | 0.18 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.12 |
mshA | 576442 | p.Cys365Trp | missense_variant | 0.34 |
mshA | 576626 | p.Thr427Pro | missense_variant | 0.17 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.31 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.38 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673162 | c.-278T>C | upstream_gene_variant | 1.0 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168863 | c.1750C>T | synonymous_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.15 |
PPE35 | 2170686 | c.-74G>A | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.32 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.25 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.57 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.22 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
Rv3236c | 3612047 | p.Ala357Val | missense_variant | 1.0 |
rpoA | 3878580 | c.-73A>C | upstream_gene_variant | 0.2 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.88 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.16 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.61 |
embB | 4246820 | p.Pro103Thr | missense_variant | 1.0 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.33 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.19 |
embB | 4247033 | p.Ser174Arg | missense_variant | 0.26 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.14 |
aftB | 4267981 | p.Arg286Gly | missense_variant | 0.21 |
ethA | 4326505 | c.969C>G | synonymous_variant | 1.0 |
ethA | 4328415 | c.-942A>G | upstream_gene_variant | 0.19 |
whiB6 | 4338200 | p.Asp108His | missense_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |