Run ID: SRR23861971
Sample name:
Date: 12-04-2023 12:53:19
Number of reads: 4672253
Percentage reads mapped: 99.69
Strain: lineage4.8
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|---|---|
Rifampicin | ||
Isoniazid | R | inhA p.Ser94Ala (1.00) |
Ethambutol | ||
Pyrazinamide | ||
Streptomycin | R | rpsL p.Lys43Arg (1.00) |
Fluoroquinolones | R | gyrB p.Asp461Asn (0.30), gyrB p.Asn499Thr (0.56) |
Moxifloxacin | R | gyrB p.Asp461Asn (0.30), gyrB p.Asn499Thr (0.56) |
Ofloxacin | R | gyrB p.Asp461Asn (0.30), gyrB p.Asn499Thr (0.56) |
Levofloxacin | R | gyrB p.Asp461Asn (0.30), gyrB p.Asn499Thr (0.56) |
Ciprofloxacin | R | gyrB p.Asp461Asn (0.30), gyrB p.Asn499Thr (0.56) |
Aminoglycosides | ||
Amikacin | ||
Capreomycin | ||
Kanamycin | ||
Cycloserine | ||
Ethionamide | R | inhA p.Ser94Ala (1.00) |
Clofazimine | ||
Para-aminosalicylic_acid | ||
Delamanid | ||
Bedaquiline | ||
Linezolid |
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 |
---|---|---|---|---|---|
gyrB | 6620 | p.Asp461Asn | missense_variant | 0.3 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
gyrB | 6735 | p.Asn499Thr | missense_variant | 0.56 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
inhA | 1674481 | p.Ser94Ala | missense_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.99 |
mshA | 576093 | p.Pro249Arg | missense_variant | 0.17 |
mshA | 576100 | p.Asp251Glu | missense_variant | 0.17 |
mshA | 576101 | p.Arg252Gly | missense_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.99 |
rrs | 1471786 | n.-60T>G | upstream_gene_variant | 0.13 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
whiB7 | 3568416 | p.Lys88His | missense_variant | 0.14 |
whiB7 | 3568428 | c.252A>C | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247395 | c.882C>T | synonymous_variant | 1.0 |
embB | 4247965 | c.1452C>T | synonymous_variant | 1.0 |
ethR | 4328030 | p.Ala161Gly | missense_variant | 0.18 |
ethR | 4328045 | p.Leu166Gln | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |