Run ID: ERR4817492
Sample name:
Date: 01-04-2023 15:01:30
Number of reads: 2594092
Percentage reads mapped: 96.42
Strain: lineage3.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
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 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_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 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.12 |
rrl | 1473390 | n.-268A>C | upstream_gene_variant | 0.15 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474774 | n.1117A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474800 | n.1143T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.44 |
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 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 0.98 |
ahpC | 2726105 | c.-88G>A | 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 |
alr | 3841575 | c.-155C>T | upstream_gene_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246629 | p.Val39Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |