Run ID: ERR4815443
Sample name:
Date: 01-04-2023 13:51:57
Number of reads: 3185309
Percentage reads mapped: 99.28
Strain: lineage4.1
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ethA | 4326426 | c.1047dupT | frameshift_variant | 1.0 | ethionamide, ethionamide |
gid | 4407865 | c.337dupG | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
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 | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473466 | n.-192G>T | upstream_gene_variant | 0.12 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474904 | n.1247G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474928 | n.1271C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.17 |
inhA | 1674427 | p.Gly76Cys | missense_variant | 0.11 |
inhA | 1674590 | p.Met130Thr | missense_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168051 | c.2562G>A | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2986875 | p.Pro13Ser | missense_variant | 1.0 |
Rv2752c | 3065854 | p.Ala113Glu | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |