Run ID: SRR7592384
Sample name:
Date: 04-04-2023 19:51:14
Number of reads: 3630179
Percentage reads mapped: 99.46
Strain: lineage4.8
Drug-resistance: Pre-XDR-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 |
---|---|---|---|---|---|
gyrA | 7581 | p.Asp94Asn | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289219 | p.Asp8Ala | missense_variant | 1.0 | pyrazinamide |
embB | 4248003 | p.Gln497Pro | missense_variant | 1.0 | ethambutol |
ethA | 4326074 | c.1014_1399del | frameshift_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.2 |
rpoC | 765425 | c.2059_2061dupCAG | conservative_inframe_insertion | 0.98 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781362 | c.-198_-197insTAT | upstream_gene_variant | 0.8 |
rpsL | 781395 | c.-165T>C | upstream_gene_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 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2170065 | p.Ala183Gly | missense_variant | 0.27 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747468 | p.Asp44Ile | missense_variant | 0.98 |
folC | 2747470 | p.Ile43Met | missense_variant | 1.0 |
pepQ | 2860159 | p.Ala87Gly | missense_variant | 0.18 |
Rv2752c | 3065335 | p.Leu286Arg | missense_variant | 1.0 |
Rv2752c | 3067110 | c.-919A>G | upstream_gene_variant | 1.0 |
ald | 3086822 | c.3G>A | start_lost | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 0.62 |
fbiD | 3339744 | c.627A>T | synonymous_variant | 0.33 |
fbiD | 3339746 | p.Ala210Gly | missense_variant | 0.37 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.69 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.24 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.3 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.2 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.29 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.29 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.14 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.12 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.4 |
ubiA | 4269292 | p.Ala181Val | missense_variant | 1.0 |
ethA | 4326052 | p.Asp474Glu | 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 |