Run ID: SRR7517717
Sample name:
Date: 04-04-2023 19:33:39
Number of reads: 1332615
Percentage reads mapped: 97.74
Strain: lineage4.1.2
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6886 | p.Phe549Leu | missense_variant | 0.25 |
gyrA | 7356 | p.Asp19Tyr | missense_variant | 0.22 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9802 | p.Asp834Ala | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
fgd1 | 491764 | p.Leu328Met | missense_variant | 0.18 |
ccsA | 620346 | c.456C>T | synonymous_variant | 0.2 |
ccsA | 620385 | c.495G>T | synonymous_variant | 0.22 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778636 | c.-156C>A | upstream_gene_variant | 0.25 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407170 | p.Phe57Leu | missense_variant | 0.24 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474602 | n.945C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476597 | n.2940G>T | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673522 | p.Gly28Val | missense_variant | 0.2 |
inhA | 1674696 | p.Lys165Asn | missense_variant | 0.29 |
inhA | 1674785 | p.Arg195Leu | missense_variant | 0.22 |
rpsA | 1833384 | c.-158C>A | upstream_gene_variant | 0.23 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154888 | p.Phe408Leu | missense_variant | 0.33 |
PPE35 | 2167712 | c.2901C>A | synonymous_variant | 0.22 |
PPE35 | 2168284 | p.Asp777Tyr | missense_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
folC | 2746786 | c.813G>A | synonymous_variant | 0.4 |
folC | 2746846 | c.753C>A | synonymous_variant | 0.2 |
folC | 2747790 | c.-192G>T | upstream_gene_variant | 0.2 |
Rv2752c | 3064818 | c.1374C>A | synonymous_variant | 0.18 |
thyX | 3067828 | p.Gly40Cys | missense_variant | 0.22 |
thyX | 3067891 | p.Ala19Ser | missense_variant | 0.18 |
thyA | 3074510 | c.-39C>A | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086921 | c.102C>A | synonymous_variant | 0.28 |
Rv3083 | 3449164 | p.Pro221Ser | missense_variant | 0.18 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3613023 | p.Pro32Thr | missense_variant | 0.17 |
fbiB | 3641546 | c.12C>A | synonymous_variant | 0.22 |
rpoA | 3877772 | p.Ser246Pro | missense_variant | 1.0 |
rpoA | 3878550 | c.-43C>A | upstream_gene_variant | 0.22 |
rpoA | 3878574 | c.-67G>T | upstream_gene_variant | 0.5 |
clpC1 | 4039016 | c.1689C>A | synonymous_variant | 0.25 |
panD | 4044114 | c.168C>A | synonymous_variant | 0.24 |
embC | 4240898 | p.Leu346Ile | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244810 | p.Phe526Leu | missense_variant | 0.22 |
embB | 4249476 | p.Trp988Leu | missense_variant | 0.2 |
aftB | 4268573 | p.Met88Ile | missense_variant | 0.25 |
ethA | 4326535 | c.939G>T | synonymous_variant | 0.21 |
whiB6 | 4338227 | p.Ala99Thr | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |