Run ID: ERR2229538
Sample name:
Date: 31-03-2023 17:18:12
Number of reads: 1201117
Percentage reads mapped: 99.31
Strain: lineage4.8
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 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155483 | c.628delT | frameshift_variant | 0.12 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.27 |
mshA | 576292 | c.945C>A | synonymous_variant | 0.15 |
mshA | 576350 | p.Asp335Tyr | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777481 | p.Thr334Ser | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.34 |
rpsA | 1834349 | p.Glu270* | stop_gained | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155312 | p.Val267Asp | missense_variant | 0.12 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.17 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.15 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.19 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.19 |
Rv1979c | 2222285 | p.Ala294Thr | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518147 | p.Phe11Leu | missense_variant | 0.12 |
kasA | 2518195 | c.81G>A | synonymous_variant | 0.12 |
kasA | 2518612 | c.498C>T | synonymous_variant | 0.12 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.14 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.14 |
eis | 2714200 | p.Lys378Arg | missense_variant | 0.1 |
pepQ | 2859601 | c.817delG | frameshift_variant | 0.12 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.15 |
ribD | 2987449 | p.Glu204Val | missense_variant | 0.18 |
Rv2752c | 3066126 | c.66C>T | synonymous_variant | 0.11 |
whiB7 | 3568430 | p.Gly84Arg | missense_variant | 0.18 |
fbiB | 3642245 | c.711C>A | synonymous_variant | 0.14 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.15 |
ddn | 3987010 | p.Thr56Asn | missense_variant | 0.21 |
embC | 4241613 | p.Thr584Ile | missense_variant | 0.18 |
embC | 4241635 | c.1773G>T | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244768 | p.Glu512Asp | missense_variant | 0.13 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.33 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.4 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.67 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.6 |
embB | 4247066 | p.Ile185Val | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |