Run ID: ERR8774378
Sample name:
Date: 02-04-2023 08:29:09
Number of reads: 3208200
Percentage reads mapped: 91.56
Strain: lineage2.2.1
Drug-resistance: MDR-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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761140 | p.His445Arg | missense_variant | 0.99 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.33 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289099 | p.Lys48Thr | missense_variant | 0.98 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
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 |
rpoC | 765050 | p.Ser561Pro | missense_variant | 1.0 |
rpoC | 766645 | p.Glu1092Asp | missense_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 | 0.98 |
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 | 1471762 | n.-84C>G | upstream_gene_variant | 0.12 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474960 | n.1303C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.31 |
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 |
clpC1 | 4038842 | c.1863G>T | synonymous_variant | 0.22 |
clpC1 | 4038850 | p.Phe619Leu | missense_variant | 0.4 |
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 |