Run ID: ERR5864679
Sample name:
Date: 01-04-2023 23:31:06
Number of reads: 1170878
Percentage reads mapped: 99.2
Strain: lineage2.2.1
Drug-resistance: MDR-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 |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781822 | p.Lys88Arg | missense_variant | 1.0 | streptomycin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
katG | 2155959 | c.152delA | frameshift_variant | 0.12 | isoniazid |
pncA | 2288941 | c.300delC | frameshift_variant | 1.0 | pyrazinamide |
eis | 2715344 | c.-12C>T | upstream_gene_variant | 1.0 | kanamycin |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
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 | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576352 | p.Asp335Glu | missense_variant | 0.12 |
ccsA | 619983 | c.93G>T | synonymous_variant | 0.13 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764363 | p.Gly332Cys | missense_variant | 1.0 |
rpoC | 764622 | p.Leu418His | missense_variant | 0.11 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777228 | p.Arg418His | missense_variant | 0.1 |
mmpL5 | 778223 | p.Asp86Glu | missense_variant | 0.1 |
mmpR5 | 779174 | p.Ala62Val | missense_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407480 | c.-140A>G | upstream_gene_variant | 0.12 |
Rv1258c | 1407511 | c.-171T>C | upstream_gene_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474582 | n.925T>A | non_coding_transcript_exon_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156234 | c.-123G>T | upstream_gene_variant | 0.11 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518155 | p.Val14Ala | missense_variant | 0.1 |
folC | 2746852 | c.747G>T | synonymous_variant | 0.12 |
folC | 2746909 | c.688_689delAC | frameshift_variant | 0.13 |
folC | 2746914 | p.Asp229Asn | missense_variant | 0.13 |
folC | 2746917 | p.Pro228Ala | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087305 | c.486G>T | synonymous_variant | 0.12 |
ald | 3087786 | p.Glu323Lys | missense_variant | 0.1 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612229 | c.888C>T | synonymous_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3642229 | p.Leu232Gln | missense_variant | 0.11 |
fbiB | 3642232 | p.Leu233Gln | missense_variant | 0.11 |
fbiB | 3642234 | p.Arg234Leu | missense_variant | 0.11 |
clpC1 | 4038269 | c.2436C>G | synonymous_variant | 0.11 |
embC | 4241999 | c.2139delG | frameshift_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4247066 | p.Ile185Val | missense_variant | 0.13 |
aftB | 4267278 | p.Arg520Gln | missense_variant | 0.12 |
aftB | 4267643 | c.1194C>T | synonymous_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268895 | c.-60delG | 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 |