Run ID: SRR6045759
Sample name:
Date: 04-04-2023 12:04:56
Number of reads: 2337111
Percentage reads mapped: 96.51
Strain: lineage2.2.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761161 | p.Leu452Pro | missense_variant | 1.0 | rifampicin |
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 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472141 | n.296G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472436 | n.591G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472437 | n.592T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472449 | n.604C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472450 | n.605A>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472451 | n.606C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472462 | n.617T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473942 | n.285G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474896 | n.1239A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474901 | n.1244A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1833410 | c.-132G>A | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3840255 | p.Glu389Gly | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |