Run ID: ERR2513919
Sample name:
Date: 31-03-2023 19:59:38
Number of reads: 2295883
Percentage reads mapped: 99.04
Strain: lineage4.6.2.2
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 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.2 | Euro-American | T;LAM | RD726 | 1.0 |
lineage4.6.2.2 | Euro-American (Cameroon) | LAM10-CAM | RD726 | 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 |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778298 | c.-692C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472487 | n.643dupT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475754 | n.2097G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475762 | n.2105G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475774 | n.2117C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476373 | n.2716A>G | non_coding_transcript_exon_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155389 | c.723C>G | synonymous_variant | 1.0 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 0.97 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyX | 3067474 | p.Pro158Ala | missense_variant | 1.0 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612571 | c.546C>T | synonymous_variant | 1.0 |
Rv3236c | 3612910 | p.Leu69Phe | missense_variant | 1.0 |
embA | 4242550 | c.-683C>G | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 1.0 |
aftB | 4268622 | p.Trp72Leu | missense_variant | 0.16 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 1.0 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |