Run ID: ERR2229130
Sample name:
Date: 31-03-2023 16:42:25
Number of reads: 1099737
Percentage reads mapped: 99.39
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 | 491281 | p.Asp167Asn | missense_variant | 0.13 |
fgd1 | 491331 | c.549G>A | synonymous_variant | 0.11 |
fgd1 | 491761 | p.Asp327Tyr | missense_variant | 0.12 |
mshA | 576639 | p.Glu431Val | missense_variant | 0.14 |
ccsA | 620440 | p.Gly184Arg | missense_variant | 0.14 |
ccsA | 620784 | c.894C>A | synonymous_variant | 0.12 |
rpoB | 761029 | p.Pro408Gln | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775674 | p.Trp936Leu | missense_variant | 0.17 |
mmpL5 | 775826 | c.2655G>A | synonymous_variant | 0.14 |
mmpL5 | 777119 | p.His454Gln | missense_variant | 0.23 |
mmpL5 | 777122 | c.1359C>T | synonymous_variant | 0.23 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.18 |
mmpL5 | 777292 | p.Ala397Ser | missense_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304224 | p.Gly432Ser | missense_variant | 0.14 |
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 | 0.2 |
inhA | 1674620 | p.Pro140Leu | missense_variant | 0.13 |
rpsA | 1834961 | c.1423delG | frameshift_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102094 | p.Val317Met | missense_variant | 0.11 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.14 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.21 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.21 |
PPE35 | 2168140 | p.Ala825Thr | missense_variant | 0.13 |
PPE35 | 2168143 | p.Phe824Leu | missense_variant | 0.13 |
PPE35 | 2168150 | c.2463T>C | synonymous_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.11 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.11 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.47 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.5 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290023 | c.-783delC | upstream_gene_variant | 0.12 |
pncA | 2290117 | c.-876C>T | upstream_gene_variant | 0.12 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.13 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.13 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.11 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.12 |
folC | 2746344 | p.Leu419Met | missense_variant | 0.12 |
thyA | 3074619 | c.-148C>A | upstream_gene_variant | 0.12 |
Rv3083 | 3448500 | c.-4A>G | upstream_gene_variant | 1.0 |
Rv3083 | 3448501 | c.-3G>T | upstream_gene_variant | 1.0 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.2 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.18 |
embC | 4242229 | c.2367C>G | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243087 | c.-146G>A | upstream_gene_variant | 0.12 |
embA | 4243665 | p.Thr145Ser | missense_variant | 0.15 |
embB | 4246511 | c.-3G>T | upstream_gene_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.57 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.44 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.56 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.6 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.6 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.4 |
embB | 4246772 | p.Val87Leu | missense_variant | 0.15 |
aftB | 4268010 | p.Leu276Pro | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |