Run ID: ERR4831837
Sample name:
Date: 01-04-2023 21:09:22
Number of reads: 1819227
Percentage reads mapped: 86.9
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761140 | p.His445Arg | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.98 | streptomycin |
katG | 2155167 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288841 | p.Ala134Val | missense_variant | 1.0 | pyrazinamide |
embA | 4243217 | c.-16C>G | upstream_gene_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 | 765509 | p.Asp714Asn | 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 | 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 | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472266 | n.421C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474584 | n.927C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474586 | n.929T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474587 | n.930G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474602 | n.945C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474608 | n.951T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474609 | n.952G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474610 | n.953C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474862 | n.1205C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475008 | n.1351C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475440 | n.1783T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476384 | n.2727G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.96 |
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 |
PPE35 | 2168435 | c.2178C>T | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714566 | p.Leu256Pro | missense_variant | 0.17 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.31 |
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 | 3878543 | c.-36G>C | upstream_gene_variant | 0.11 |
rpoA | 3878615 | c.-108C>T | upstream_gene_variant | 1.0 |
rpoA | 3878633 | c.-126C>A | upstream_gene_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4249738 | c.3225C>T | synonymous_variant | 0.12 |
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 |