Run ID: ERR4832040
Sample name:
Date: 01-04-2023 21:17:10
Number of reads: 901474
Percentage reads mapped: 99.73
Strain: lineage2.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.1 | East-Asian (non-Beijing) | None | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embA | 4243217 | c.-16C>T | upstream_gene_variant | 1.0 | ethambutol |
ethA | 4326166 | c.1307delC | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8848 | p.Val516Ala | missense_variant | 0.1 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575851 | c.504C>T | synonymous_variant | 1.0 |
mshA | 576318 | p.Arg324Gln | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 765121 | c.1752G>A | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304159 | p.Val410Gly | missense_variant | 0.17 |
fbiC | 1304443 | p.Ala505Thr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472297 | n.452G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472795 | n.950T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474500 | n.843T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475587 | n.1930G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.16 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168696 | c.1917C>T | synonymous_variant | 0.25 |
PPE35 | 2168955 | p.Phe553Ser | missense_variant | 0.12 |
PPE35 | 2169673 | p.Ser314Pro | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289898 | c.-657C>T | upstream_gene_variant | 1.0 |
kasA | 2518924 | c.810C>A | synonymous_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.23 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.3 |
ahpC | 2726350 | p.Trp53Leu | missense_variant | 0.18 |
Rv2752c | 3065616 | c.576C>T | synonymous_variant | 1.0 |
thyA | 3074645 | c.-174T>G | upstream_gene_variant | 0.27 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878489 | p.Pro7Ser | missense_variant | 0.12 |
clpC1 | 4040841 | c.-138delG | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243007 | p.Leu1049Val | missense_variant | 1.0 |
embB | 4246088 | c.-426A>G | upstream_gene_variant | 1.0 |
embB | 4246277 | c.-237G>A | upstream_gene_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 | 4408002 | c.191_200delGGGTCGTGGA | frameshift_variant | 1.0 |