Run ID: SRR2101767
Sample name:
Date: 03-04-2023 23:54:17
Number of reads: 461485
Percentage reads mapped: 95.69
Strain: lineage4.1.2.1
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 | 0.94 |
lineage4.1.2 | Euro-American | T;H | None | 0.91 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.87 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155740 | c.371delG | frameshift_variant | 0.1 | isoniazid, isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7580 | c.279C>T | synonymous_variant | 0.91 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.88 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.93 |
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 | 1.0 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472669 | n.824_825insTAG | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472677 | n.832C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472678 | n.833T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472684 | n.841_846delGATCCG | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472700 | n.855C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472705 | n.860G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.17 |
inhA | 1674498 | c.297G>C | synonymous_variant | 0.92 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.17 |
Rv1979c | 2223051 | p.Glu38Asp | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.9 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
panD | 4044308 | c.-27A>T | upstream_gene_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.96 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |