Run ID: ERR2229357
Sample name:
Date: 31-03-2023 17:05:19
Number of reads: 1472074
Percentage reads mapped: 98.98
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 |
gyrA | 9164 | c.1863G>A | synonymous_variant | 0.11 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.41 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.2 |
mshA | 576259 | c.912C>T | synonymous_variant | 0.13 |
ccsA | 620842 | p.His318Asp | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776882 | p.Ile533Met | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304428 | c.1498C>A | synonymous_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 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.23 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101830 | p.Ile405Phe | missense_variant | 0.12 |
ndh | 2103109 | c.-67C>T | upstream_gene_variant | 0.11 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.18 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169066 | p.Ala516Val | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.56 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.57 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.21 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.21 |
kasA | 2519306 | p.Val398Ile | missense_variant | 0.13 |
eis | 2714845 | p.Val163Asp | missense_variant | 0.12 |
pepQ | 2859762 | p.Lys219Asn | missense_variant | 0.12 |
pepQ | 2860153 | p.Glu89Ala | missense_variant | 0.17 |
Rv2752c | 3064777 | p.Phe472Ser | missense_variant | 0.11 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.18 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
clpC1 | 4039018 | p.Ser563Ala | missense_variant | 0.15 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.2 |
clpC1 | 4039498 | p.Ile403Val | missense_variant | 0.2 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243096 | c.-137A>C | upstream_gene_variant | 0.1 |
embA | 4244920 | p.Leu563Pro | missense_variant | 0.13 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.32 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.47 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.47 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.31 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.21 |
aftB | 4267866 | p.Leu324Arg | missense_variant | 0.12 |
aftB | 4267900 | p.Ala313Ser | missense_variant | 0.22 |
aftB | 4268213 | c.624T>C | synonymous_variant | 0.17 |
aftB | 4268810 | c.27G>C | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408406 | c.-204A>G | upstream_gene_variant | 0.12 |
Rv3083 | 3448498 | c.-5_*1408del | transcript_ablation | 1.0 |