Run ID: ERR2514109
Sample name:
Date: 31-03-2023 20:07:24
Number of reads: 444540
Percentage reads mapped: 99.53
Strain: lineage2.2.1
Drug-resistance: HR-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 |
---|---|---|---|---|---|
katG | 2154172 | c.1939delA | frameshift_variant | 0.12 | isoniazid |
embB | 4247622 | p.Leu370Arg | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6043 | c.804G>A | synonymous_variant | 0.11 |
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 | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760076 | c.270C>T | synonymous_variant | 0.15 |
rpoB | 760301 | c.495C>A | synonymous_variant | 0.11 |
rpoB | 761299 | p.Ala498Glu | missense_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764242 | c.873C>T | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776158 | p.Asp775His | missense_variant | 0.13 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302984 | c.54G>T | synonymous_variant | 0.13 |
fbiC | 1305302 | p.Leu791Pro | missense_variant | 0.12 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473086 | n.1244delA | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476061 | n.2404T>C | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1674151 | p.Pro238Thr | missense_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102816 | p.Leu76Pro | missense_variant | 0.12 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.4 |
katG | 2154088 | p.Asp675Gly | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168524 | p.Gly697Ser | missense_variant | 0.17 |
Rv1979c | 2222300 | p.Val289Met | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726495 | p.Asn101Lys | missense_variant | 0.22 |
folC | 2746526 | p.Gly358Val | missense_variant | 0.14 |
pepQ | 2860208 | p.Leu71Val | missense_variant | 0.18 |
Rv2752c | 3064589 | p.Arg535Ser | missense_variant | 0.25 |
thyA | 3074554 | c.-83G>A | upstream_gene_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339569 | p.Leu151Pro | missense_variant | 0.29 |
Rv3083 | 3449458 | p.Asp319Asn | missense_variant | 0.15 |
fprA | 3473906 | c.-101A>G | upstream_gene_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640386 | c.-157A>G | upstream_gene_variant | 0.22 |
rpoA | 3878425 | p.Pro28Leu | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245169 | p.Val646Ala | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4326491 | p.Asn328Ile | missense_variant | 0.1 |
ethA | 4326676 | p.Ser266Arg | 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 |