Run ID: SRR7645919
Sample name:
Date: 04-04-2023 19:58:29
Number of reads: 1994207
Percentage reads mapped: 99.68
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 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4248003 | p.Gln497Pro | missense_variant | 1.0 | ethambutol |
embB | 4249583 | p.Asp1024Asn | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8941 | c.1644delG | frameshift_variant | 0.17 |
fgd1 | 491313 | c.531C>T | synonymous_variant | 0.18 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.1 |
rpoC | 766367 | p.Ala1000Thr | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777290 | c.1191G>A | synonymous_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302891 | c.-40G>A | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472151 | n.306C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473203 | n.1358G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473968 | n.315delG | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474654 | n.997C>T | non_coding_transcript_exon_variant | 0.18 |
inhA | 1674952 | p.Pro251Ala | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169909 | p.Asn235Ile | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3065959 | c.232delG | frameshift_variant | 0.11 |
fbiD | 3339561 | c.444C>A | synonymous_variant | 0.11 |
fprA | 3474424 | c.419delA | frameshift_variant | 0.12 |
fbiA | 3641030 | p.Ser163Asn | missense_variant | 0.13 |
fbiB | 3642535 | p.Arg334Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247395 | c.882C>T | synonymous_variant | 1.0 |
ethA | 4326704 | p.Pro257Gln | missense_variant | 0.95 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407967 | p.Leu79Trp | missense_variant | 1.0 |
gid | 4408060 | p.His48Arg | missense_variant | 0.4 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |