Run ID: ERR4813750
Sample name:
Date: 01-04-2023 12:58:14
Number of reads: 3205812
Percentage reads mapped: 99.68
Strain: lineage4.1.2;lineage2.2.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.91 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.07 |
lineage4.1 | Euro-American | T;X;H | None | 0.06 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.92 |
lineage4.1.2 | Euro-American | T;H | None | 0.06 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.92 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472362 | n.517C>T | non_coding_transcript_exon_variant | 0.9 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.93 | 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 | 0.92 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.89 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.87 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.86 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.92 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.9 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.85 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.86 |
rrs | 1471647 | n.-199G>A | upstream_gene_variant | 0.92 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.9 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.9 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.93 |
PPE35 | 2168963 | c.1650A>G | synonymous_variant | 0.15 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 0.24 |
PPE35 | 2169059 | c.1554G>A | synonymous_variant | 0.19 |
PPE35 | 2169063 | p.Met517Thr | missense_variant | 0.18 |
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 | 0.93 |
alr | 3840263 | c.1158C>T | synonymous_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.93 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.97 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.88 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.91 |