Run ID: ERR2229178
Sample name:
Date: 31-03-2023 16:47:32
Number of reads: 869024
Percentage reads mapped: 99.08
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 | 6689 | p.Lys484Glu | missense_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491142 | c.360C>T | synonymous_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.25 |
mshA | 576513 | p.Leu389Gln | missense_variant | 0.4 |
rpoB | 762733 | p.Glu976Val | missense_variant | 0.18 |
rpoB | 762870 | p.Met1022Val | missense_variant | 0.11 |
rpoC | 763730 | c.365delC | frameshift_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776017 | p.Ile822Leu | missense_variant | 0.12 |
mmpL5 | 776728 | p.Phe585Leu | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1416963 | c.384delC | frameshift_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.38 |
inhA | 1674394 | p.Val65Leu | missense_variant | 0.29 |
inhA | 1674699 | p.Ser166Arg | missense_variant | 0.14 |
rpsA | 1834052 | p.Ala171Ser | missense_variant | 0.17 |
rpsA | 1834345 | p.Asp268Glu | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102148 | c.895C>A | synonymous_variant | 0.14 |
katG | 2155294 | p.Gly273Val | missense_variant | 0.2 |
PPE35 | 2167773 | p.Gly947Val | missense_variant | 0.22 |
PPE35 | 2167833 | p.Leu927Arg | missense_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.16 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.16 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.16 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.15 |
PPE35 | 2170159 | p.Ala152Ser | missense_variant | 0.21 |
PPE35 | 2170381 | p.Ala78Ser | missense_variant | 0.15 |
PPE35 | 2170382 | p.Ala77Gly | missense_variant | 0.14 |
PPE35 | 2170387 | c.226C>T | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289714 | c.-473G>T | upstream_gene_variant | 0.17 |
kasA | 2518348 | c.234A>T | synonymous_variant | 0.12 |
kasA | 2518486 | c.372G>A | synonymous_variant | 0.2 |
kasA | 2518723 | c.609G>A | synonymous_variant | 0.33 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.13 |
thyX | 3067800 | p.Lys49Thr | missense_variant | 0.14 |
Rv3236c | 3612286 | c.831A>G | synonymous_variant | 0.17 |
fbiB | 3640563 | c.-972C>T | upstream_gene_variant | 0.14 |
fbiB | 3642232 | c.700_701delCG | frameshift_variant | 0.13 |
clpC1 | 4039355 | c.1350G>T | synonymous_variant | 0.11 |
panD | 4043926 | p.His119Leu | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.33 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.33 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.33 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.38 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.29 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.29 |
ubiA | 4269001 | p.Ala278Val | missense_variant | 0.13 |
ubiA | 4269446 | p.Val130Ile | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |