Run ID: ERR2229139
Sample name:
Date: 31-03-2023 16:43:53
Number of reads: 891191
Percentage reads mapped: 97.96
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 |
---|---|---|---|---|
gyrB | 5788 | c.549G>C | synonymous_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491336 | p.Ala185Val | missense_variant | 0.14 |
fgd1 | 491716 | p.Ala312Pro | missense_variant | 0.13 |
rpoC | 766981 | c.3612T>C | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775735 | p.Phe916Leu | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303562 | c.635delG | frameshift_variant | 0.13 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304822 | p.His631Arg | missense_variant | 0.11 |
embR | 1416890 | p.Leu153Pro | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476686 | n.3029C>T | non_coding_transcript_exon_variant | 0.17 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.14 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.15 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.15 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.24 |
rpsA | 1834964 | c.1428delA | frameshift_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154699 | p.Gln471His | missense_variant | 0.12 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.14 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.14 |
PPE35 | 2167973 | c.2640A>G | synonymous_variant | 0.25 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.16 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.55 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.52 |
Rv1979c | 2223010 | p.Val52Gly | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714773 | p.Pro187Leu | missense_variant | 0.18 |
pepQ | 2859733 | p.Tyr229Phe | missense_variant | 0.15 |
pepQ | 2860186 | p.Ala78Val | missense_variant | 0.22 |
pepQ | 2860259 | p.Leu54Met | missense_variant | 0.14 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.13 |
alr | 3840341 | c.1080C>G | synonymous_variant | 0.18 |
rpoA | 3878599 | c.-92C>G | upstream_gene_variant | 1.0 |
clpC1 | 4039054 | p.Phe551Leu | missense_variant | 0.17 |
panD | 4044289 | c.-8A>T | upstream_gene_variant | 0.12 |
panD | 4044350 | c.-69C>T | upstream_gene_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243083 | p.Asp1074Ala | missense_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.75 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.4 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.4 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.4 |
embB | 4247073 | p.Gly187Glu | missense_variant | 0.18 |
ethA | 4326885 | p.Ser197Pro | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |