Run ID: ERR4816419
Sample name:
Date: 01-04-2023 14:25:12
Number of reads: 1017382
Percentage reads mapped: 97.45
Strain: lineage2.2.1
Drug-resistance: HR-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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.36 | streptomycin |
katG | 2155541 | p.Trp191Arg | missense_variant | 0.12 | isoniazid |
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 | 491027 | p.Asn82Thr | missense_variant | 0.25 |
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 | 778626 | c.279_280insGTGAGCG | frameshift_variant | 0.12 |
mmpS5 | 778630 | p.Leu92Phe | missense_variant | 0.11 |
mmpS5 | 778632 | c.267_273delGCTCACC | frameshift_variant | 0.12 |
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 | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472687 | n.842A>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473008 | n.1164delT | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476523 | n.2867delC | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102914 | c.129C>A | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.21 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714526 | c.805_806delAC | frameshift_variant | 1.0 |
Rv2752c | 3065711 | p.Gly161Ser | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448650 | c.147C>T | synonymous_variant | 0.1 |
Rv3083 | 3449095 | p.Gly198Ser | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | 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 |