Run ID: ERR2229115
Sample name:
Date: 31-03-2023 16:40:59
Number of reads: 666324
Percentage reads mapped: 99.45
Strain: lineage4.8
Drug-resistance: Other
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 |
---|---|---|---|---|---|
pncA | 2289030 | p.His71Arg | missense_variant | 0.11 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7413 | p.Gly38Ser | missense_variant | 0.17 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.23 |
rpoB | 759841 | p.Ser12Asn | missense_variant | 0.29 |
rpoB | 761504 | c.1698C>A | synonymous_variant | 0.14 |
rpoB | 761746 | p.Val647Ala | missense_variant | 0.12 |
rpoB | 762393 | p.Val863Met | missense_variant | 0.17 |
rpoC | 766219 | p.Asp950Glu | missense_variant | 0.17 |
rpoC | 766932 | p.Ala1188Val | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776209 | p.Leu758Met | missense_variant | 0.22 |
mmpL5 | 777128 | c.1353A>G | synonymous_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304498 | p.Pro523Leu | missense_variant | 0.15 |
fbiC | 1305183 | p.Leu751Phe | missense_variant | 0.17 |
embR | 1416481 | c.867G>A | synonymous_variant | 0.18 |
embR | 1416798 | p.Cys184Arg | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474302 | n.645G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475951 | n.2294G>A | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.23 |
inhA | 1674661 | p.Ala154Thr | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102696 | p.Ile116Asn | missense_variant | 0.15 |
katG | 2155959 | p.Asn51Lys | missense_variant | 0.13 |
PPE35 | 2167955 | c.2658A>C | synonymous_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169902 | c.711G>C | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.33 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.35 |
PPE35 | 2170368 | p.Gln82Arg | missense_variant | 0.14 |
PPE35 | 2170372 | p.Thr81Ala | missense_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223333 | c.-169G>A | upstream_gene_variant | 0.12 |
kasA | 2518899 | p.Leu262Trp | missense_variant | 0.2 |
Rv2752c | 3064875 | c.1317C>T | synonymous_variant | 0.17 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.42 |
whiB7 | 3568757 | c.-78A>G | upstream_gene_variant | 0.5 |
fbiA | 3640880 | p.Leu113Arg | missense_variant | 0.2 |
fbiA | 3640888 | c.349delC | frameshift_variant | 0.2 |
fbiB | 3641899 | p.Pro122Leu | missense_variant | 0.12 |
alr | 3840558 | p.Arg288Leu | missense_variant | 0.22 |
clpC1 | 4039094 | c.1611C>T | synonymous_variant | 0.18 |
embC | 4240859 | c.997C>T | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248976 | c.2463G>C | synonymous_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408197 | c.6T>A | synonymous_variant | 0.17 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |