Run ID: ERR4831890
Sample name:
Date: 01-04-2023 21:11:27
Number of reads: 935290
Percentage reads mapped: 99.66
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 | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5573 | p.Asp112Tyr | missense_variant | 0.15 |
gyrA | 6385 | c.-917G>C | upstream_gene_variant | 0.13 |
gyrB | 6521 | p.Arg428Trp | missense_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 | 759670 | c.-137C>T | upstream_gene_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763080 | p.Gly1092Cys | missense_variant | 0.12 |
rpoC | 764376 | p.Ala336Gly | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 778184 | c.-806C>A | upstream_gene_variant | 0.11 |
mmpR5 | 779257 | p.Arg90Cys | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303701 | c.771C>A | synonymous_variant | 0.12 |
fbiC | 1303748 | p.Thr273Lys | missense_variant | 0.15 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1417239 | p.Ala37Ser | missense_variant | 0.14 |
embR | 1417276 | c.72C>T | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475914 | n.2257C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476042 | n.2387delT | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476712 | n.3055C>A | non_coding_transcript_exon_variant | 0.18 |
rpsA | 1833849 | p.Ser103Tyr | missense_variant | 0.13 |
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 | 0.29 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168618 | c.1995G>A | synonymous_variant | 0.14 |
Rv1979c | 2222692 | p.Ala158Glu | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.29 |
thyA | 3074105 | p.Pro123Ser | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087675 | p.Pro286Thr | missense_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568503 | c.177G>T | synonymous_variant | 0.12 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878255 | p.Val85Met | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethA | 4326377 | p.Thr366Met | missense_variant | 0.2 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 1.0 |
ethA | 4327094 | p.Ser127Ile | missense_variant | 0.11 |
ethR | 4327462 | c.-87G>A | upstream_gene_variant | 0.15 |
ethA | 4327644 | c.-171G>T | upstream_gene_variant | 0.14 |
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 |