Run ID: SRR1166818
Sample name:
Date: 03-04-2023 01:26:53
Number of reads: 1276141
Percentage reads mapped: 98.79
Strain: lineage4.8
Drug-resistance: MDR-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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288805 | p.Ala146Val | missense_variant | 1.0 | pyrazinamide |
embB | 4247729 | p.Gly406Ser | missense_variant | 1.0 | ethambutol |
embB | 4249583 | p.Asp1024Asn | missense_variant | 1.0 | ethambutol |
gid | 4407830 | p.Gln125* | stop_gained | 0.97 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoC | 764817 | p.Val483Ala | missense_variant | 1.0 |
rpoC | 765008 | p.Leu547Val | missense_variant | 1.0 |
rpoC | 766085 | p.Pro906Ala | missense_variant | 1.0 |
rpoC | 766611 | p.Ser1081Tyr | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1460992 | c.-53A>C | upstream_gene_variant | 0.98 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1674110 | p.Leu224Pro | missense_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.25 |
PPE35 | 2170100 | c.513G>T | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518791 | p.Ala226Val | missense_variant | 0.11 |
thyA | 3074616 | c.-145T>C | upstream_gene_variant | 0.12 |
thyA | 3074637 | c.-166A>G | upstream_gene_variant | 0.15 |
thyA | 3074641 | c.-170C>A | upstream_gene_variant | 0.17 |
fprA | 3474987 | c.981G>T | synonymous_variant | 0.12 |
alr | 3840764 | c.657G>C | synonymous_variant | 1.0 |
embC | 4241045 | p.Gly395Cys | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248053 | p.Pro514Ser | missense_variant | 0.12 |
aftB | 4267407 | p.Lys477Arg | missense_variant | 0.1 |
ethA | 4326918 | p.Thr186Pro | missense_variant | 1.0 |
ethR | 4327036 | c.-513G>T | upstream_gene_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |