Run ID: ERR4831532
Sample name:
Date: 01-04-2023 20:59:41
Number of reads: 1657195
Percentage reads mapped: 44.85
Strain: lineage2.2.2
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 |
lineage2.2.2 | East-Asian (Beijing) | Beijing-RD105/RD207 | RD105;RD207 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rrs | 1472359 | n.514A>C | non_coding_transcript_exon_variant | 0.98 | streptomycin |
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.97 | kanamycin, capreomycin, aminoglycosides, amikacin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289202 | p.Cys14Arg | missense_variant | 1.0 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
ethA | 4326333 | p.Ala381Pro | missense_variant | 1.0 | ethionamide |
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | streptomycin |
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 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.19 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764817 | p.Val483Gly | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472733 | n.888G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472742 | n.897C>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473124 | n.1279A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473147 | n.1302G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473179 | n.1334C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2153933 | p.Ala727Ser | missense_variant | 0.23 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.22 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.29 |
Rv1979c | 2221939 | p.Arg409Gln | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2987307 | p.Ala157Pro | missense_variant | 0.14 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.11 |
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 |
rpoA | 3878641 | c.-135delG | upstream_gene_variant | 0.17 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.24 |
embC | 4239842 | c.-21C>A | upstream_gene_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242822 | p.Val987Gly | missense_variant | 0.23 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269089 | p.Ala249Thr | 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 |