Run ID: ERR2041695
Sample name:
Date: 18-08-2022 09:23:06
Number of reads: 390927
Percentage reads mapped: 99.65
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.99 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289222 | p.Val7Gly | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.13 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7630 | p.Val110Glu | missense_variant | 0.17 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
rpoB | 760584 | p.Asn260Tyr | missense_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764916 | p.Leu516Pro | missense_variant | 1.0 |
rpoC | 765282 | p.Thr638Asn | missense_variant | 0.12 |
rpoC | 765517 | c.2148C>T | synonymous_variant | 0.12 |
rpoC | 765595 | c.2226G>A | synonymous_variant | 0.11 |
rpoC | 765667 | p.Asn766Lys | missense_variant | 0.11 |
rpoC | 766085 | p.Pro906Thr | missense_variant | 0.12 |
rpoC | 766333 | c.2964G>A | synonymous_variant | 0.14 |
mmpR5 | 779206 | p.Met73Val | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrl | 1475519 | n.1862G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475855 | n.2198A>G | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673619 | p.Cys60* | stop_gained | 0.12 |
inhA | 1674156 | c.-46C>T | upstream_gene_variant | 0.11 |
rpsA | 1833359 | c.-182delG | upstream_gene_variant | 0.15 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834547 | c.1007delA | frameshift_variant | 0.15 |
rpsA | 1834902 | p.Ala454Val | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154566 | p.Lys516Glu | missense_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155144 | p.Asn323Ile | missense_variant | 0.14 |
kasA | 2519043 | p.Ala310Glu | missense_variant | 0.13 |
pepQ | 2859766 | p.Val218Ala | missense_variant | 0.12 |
ribD | 2986918 | p.Glu27Gly | missense_variant | 0.12 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiA | 3641280 | p.Ile246Met | missense_variant | 0.11 |
fbiB | 3642478 | p.Asp315Val | missense_variant | 0.12 |
alr | 3841287 | p.Ile45Thr | missense_variant | 0.2 |
embC | 4239828 | c.-35G>T | upstream_gene_variant | 0.11 |
embC | 4239989 | c.127C>T | synonymous_variant | 0.12 |
embC | 4240073 | c.212delA | frameshift_variant | 0.15 |
embC | 4240856 | p.Ala332Pro | missense_variant | 0.14 |
embC | 4241565 | p.Ile568Thr | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243123 | c.-110T>C | upstream_gene_variant | 0.12 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244375 | c.1143C>T | synonymous_variant | 0.11 |
embB | 4247179 | c.666C>T | synonymous_variant | 0.11 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |