Run ID: SRR7517756
Sample name:
Date: 04-04-2023 19:36:16
Number of reads: 1963824
Percentage reads mapped: 97.41
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 | 761161 | p.Leu452Pro | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | 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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
ccsA | 620778 | c.888T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763073 | p.Asp1089Glu | missense_variant | 0.14 |
rpoB | 763147 | p.Ser1114* | stop_gained | 0.31 |
rpoC | 763478 | p.Arg37Ser | missense_variant | 0.17 |
rpoC | 765140 | p.Glu591Gln | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.96 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776142 | p.Gly780Val | missense_variant | 0.17 |
mmpL5 | 776459 | c.2022G>T | synonymous_variant | 0.2 |
mmpL5 | 776911 | p.Glu524* | stop_gained | 0.29 |
mmpL5 | 776951 | c.1530G>T | synonymous_variant | 0.22 |
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 | 1471795 | n.-51C>A | upstream_gene_variant | 0.5 |
rrs | 1471902 | n.57C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471975 | n.130G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472849 | n.1004C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472902 | n.1057C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472907 | n.1062C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473226 | n.1381C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474604 | n.947G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474619 | n.962G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474895 | n.1238C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474956 | n.1299C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475514 | n.1857G>T | non_coding_transcript_exon_variant | 0.5 |
inhA | 1673493 | c.-709C>A | upstream_gene_variant | 0.36 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102727 | p.His106Asn | missense_variant | 0.19 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168838 | p.Pro592Gln | missense_variant | 0.2 |
PPE35 | 2168927 | c.1686G>T | synonymous_variant | 0.2 |
PPE35 | 2169796 | p.Gly273Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289887 | c.-649_-647delCCG | 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 | 0.97 |
fbiB | 3640581 | c.-954C>A | upstream_gene_variant | 1.0 |
alr | 3841588 | c.-168C>A | upstream_gene_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4249739 | p.Ala1076Thr | missense_variant | 0.18 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268614 | p.Gly75Trp | missense_variant | 0.2 |
ethA | 4326403 | p.Asp357Glu | missense_variant | 0.14 |
ethA | 4327265 | p.Thr70Ile | missense_variant | 0.15 |
whiB6 | 4338501 | c.21A>G | synonymous_variant | 0.1 |
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 |