Run ID: ERR4817313
Sample name:
Date: 01-04-2023 14:55:17
Number of reads: 5107823
Percentage reads mapped: 95.41
Strain: lineage4.2.1.1
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 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
lineage4.2.1.1 | Euro-American (TUR) | H3;H4 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.3 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288957 | p.Tyr95* | stop_gained | 1.0 | pyrazinamide |
ethA | 4327409 | p.His22Pro | missense_variant | 1.0 | ethionamide |
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 |
mshA | 575833 | c.486C>T | synonymous_variant | 1.0 |
mshA | 576092 | p.Pro249Ala | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.98 |
mmpL5 | 777451 | p.Val344Leu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800973 | c.165C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471755 | n.-91C>T | upstream_gene_variant | 1.0 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169879 | p.Phe245Cys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449132 | p.Leu210Arg | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
ddn | 3987092 | p.Glu83Asp | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246587 | p.Gly25Ala | missense_variant | 1.0 |
embB | 4247790 | p.Ser426Asn | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407969 | c.233dupC | frameshift_variant | 1.0 |
gid | 4408213 | c.-11C>T | upstream_gene_variant | 1.0 |