Run ID: ERR2229416
Sample name:
Date: 12-08-2022 14:37:44
Number of reads: 1919086
Percentage reads mapped: 99.32
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 |
mshA | 575660 | p.Pro105Thr | missense_variant | 0.13 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.32 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.2 |
rpoC | 767049 | p.Gln1227Arg | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775743 | p.Gly913Val | missense_variant | 0.12 |
mmpS5 | 778835 | p.Thr24Lys | missense_variant | 0.12 |
mmpL5 | 778926 | c.-446A>G | upstream_gene_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473614 | n.-44C>A | upstream_gene_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.43 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.43 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289865 | c.-624C>A | upstream_gene_variant | 0.14 |
kasA | 2518982 | p.Ala290Ser | missense_variant | 0.11 |
kasA | 2519255 | p.Asp381Asn | missense_variant | 0.13 |
kasA | 2519277 | p.Glu388Gly | missense_variant | 0.11 |
eis | 2714834 | p.Arg167* | stop_gained | 0.2 |
eis | 2714839 | p.Leu165Trp | missense_variant | 0.2 |
Rv2752c | 3067092 | c.-901C>A | upstream_gene_variant | 0.13 |
panD | 4044193 | p.Ala30Asp | missense_variant | 0.14 |
panD | 4044311 | c.-30G>T | upstream_gene_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244305 | p.Arg358Leu | missense_variant | 0.14 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.15 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.38 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.43 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.43 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.33 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.19 |
embB | 4246747 | p.Asp78Glu | missense_variant | 0.12 |
aftB | 4267933 | p.Ala302Pro | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |