Run ID: ERR4769406
Sample name:
Date: 01-04-2023 06:39:16
Number of reads: 55085
Percentage reads mapped: 3.91
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.96 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.92 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472443 | n.598A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472446 | n.601T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472466 | n.621C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472467 | n.622G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473134 | n.1289T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473135 | n.1290C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473282 | n.1437C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473814 | n.157A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473830 | n.173T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474414 | n.757C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474450 | n.793T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475761 | n.2104C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475767 | n.2110G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.75 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156465 | c.-354C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |