Run ID: ERR2229057
Sample name:
Date: 31-03-2023 16:33:40
Number of reads: 466735
Percentage reads mapped: 98.71
Strain: lineage4
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155193 | p.Gly307Arg | missense_variant | 0.5 | isoniazid |
pncA | 2288730 | p.Ala171Glu | missense_variant | 0.17 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5856 | p.Ile206Asn | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 575341 | c.-7T>C | upstream_gene_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.5 |
rpoB | 759764 | c.-43T>A | upstream_gene_variant | 0.22 |
rpoC | 763316 | c.-54T>C | upstream_gene_variant | 0.13 |
rpoC | 763934 | p.Ala189Ser | missense_variant | 0.15 |
rpoC | 765939 | p.Arg857Leu | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
atpE | 1460999 | c.-46C>A | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471806 | n.-40T>C | upstream_gene_variant | 0.18 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475326 | n.1669A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476639 | n.2982G>A | non_coding_transcript_exon_variant | 0.29 |
fabG1 | 1673200 | c.-240C>T | upstream_gene_variant | 0.14 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155520 | p.Trp198Arg | missense_variant | 0.14 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169127 | p.Val496Ile | missense_variant | 0.18 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.13 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.14 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.17 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.18 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.17 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.17 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.22 |
PPE35 | 2169717 | p.Asn299Ile | missense_variant | 0.15 |
PPE35 | 2169725 | c.888T>C | synonymous_variant | 0.11 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.4 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.44 |
PPE35 | 2170244 | c.369G>A | synonymous_variant | 0.15 |
PPE35 | 2170249 | p.Ile122Leu | missense_variant | 0.14 |
PPE35 | 2170298 | c.315A>G | synonymous_variant | 0.14 |
PPE35 | 2170308 | p.Leu102Ala | missense_variant | 0.17 |
PPE35 | 2170313 | c.300G>C | synonymous_variant | 0.15 |
Rv1979c | 2222940 | c.224delA | frameshift_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3064740 | c.1452C>A | synonymous_variant | 0.22 |
thyA | 3073974 | c.498C>T | synonymous_variant | 0.2 |
ald | 3086703 | c.-117T>C | upstream_gene_variant | 0.12 |
embC | 4241416 | c.1554C>T | synonymous_variant | 0.22 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.6 |
embB | 4246747 | p.Asp78Glu | missense_variant | 0.27 |
embB | 4247964 | p.Ala484Asp | missense_variant | 0.17 |
embB | 4248053 | p.Pro514Ser | missense_variant | 0.29 |
embB | 4249629 | p.Ile1039Asn | missense_variant | 0.2 |
aftB | 4267205 | c.1632G>A | synonymous_variant | 0.17 |
aftB | 4269066 | c.-230C>A | upstream_gene_variant | 0.17 |
ubiA | 4269967 | c.-134C>T | upstream_gene_variant | 0.18 |
ethR | 4327760 | p.Val71Glu | missense_variant | 0.21 |
whiB6 | 4338589 | c.-68G>T | upstream_gene_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407605 | p.Ala200Thr | missense_variant | 0.22 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |