Run ID: ERR2027285
Sample name:
Date: 31-03-2023 15:42:05
Number of reads: 2084995
Percentage reads mapped: 98.79
Strain: lineage4.6.2.2
Drug-resistance: MDR-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 | 0.99 |
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 |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Cys | missense_variant | 1.0 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.54 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ethA | 4327404 | p.Gln24* | stop_gained | 1.0 | ethionamide |
gid | 4408087 | c.115delC | 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 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.2 |
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 | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472354 | n.509C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472356 | n.511A>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472364 | n.519C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472891 | n.1047delT | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474067 | n.410G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474467 | n.811delG | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474476 | n.819C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474479 | n.822A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474483 | n.826C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474540 | n.883T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474551 | n.894G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474555 | n.898T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474558 | n.901G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474581 | n.924C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474601 | n.944C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474773 | n.1116C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474783 | n.1126G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474794 | n.1137C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474852 | n.1195T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474890 | n.1233C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474977 | n.1320T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.29 |
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 | 1.0 |
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 |
clpC1 | 4040469 | p.Pro79Gln | 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 |
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 |