Run ID: ERR4799793
Sample name:
Date: 01-04-2023 09:22:21
Number of reads: 3542073
Percentage reads mapped: 99.36
Strain: lineage4.2.2.2
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.97 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.97 |
lineage4.2.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.95 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 0.96 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.98 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 0.98 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 0.91 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.98 | isoniazid |
pncA | 2289090 | p.His51Arg | missense_variant | 0.96 | pyrazinamide |
folC | 2747141 | p.Glu153Ala | missense_variant | 0.98 | para-aminosalicylic_acid |
embB | 4247429 | p.Met306Val | missense_variant | 0.94 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8688 | p.Ala463Ser | missense_variant | 0.91 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.99 |
mshA | 576077 | c.730C>T | synonymous_variant | 0.92 |
rpoB | 761293 | p.Val496Ala | missense_variant | 0.98 |
rpoB | 761489 | c.1683G>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779101 | p.Arg38* | stop_gained | 0.97 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472804 | n.959G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473787 | n.130C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474678 | n.1021G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474738 | n.1081G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474758 | n.1101G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475378 | n.1721A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475597 | n.1940G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476145 | n.2488G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476448 | n.2791G>A | non_coding_transcript_exon_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.98 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289433 | c.-192C>T | upstream_gene_variant | 0.98 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 0.91 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.98 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.98 |
embB | 4246725 | p.Leu71Pro | missense_variant | 0.97 |
ubiA | 4269148 | p.Val229Ala | missense_variant | 0.92 |
whiB6 | 4338382 | p.Asp47Gly | missense_variant | 0.96 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |