Run ID: SRR11972244
Sample name:
Date: 03-04-2023 05:33:14
Number of reads: 163067
Percentage reads mapped: 99.3
Strain:
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.98 |
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 |
embB | 4247730 | p.Gly406Ala | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 | 576259 | c.912C>T | synonymous_variant | 0.67 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620794 | p.Ala302Ser | missense_variant | 0.13 |
rpoB | 759867 | p.Ser21Pro | missense_variant | 0.22 |
rpoB | 760040 | c.234T>C | synonymous_variant | 0.3 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763827 | p.Ala153Val | missense_variant | 0.67 |
rpoC | 764058 | p.Ala230Val | missense_variant | 1.0 |
rpoC | 764916 | p.Leu516Pro | missense_variant | 1.0 |
rpoC | 765659 | p.Ala764Thr | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471890 | n.45G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473229 | n.1384T>C | non_coding_transcript_exon_variant | 0.15 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834559 | p.Val340Ile | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918449 | c.510C>T | synonymous_variant | 0.4 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156203 | c.-92C>A | upstream_gene_variant | 0.25 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168496 | p.Ile706Thr | missense_variant | 0.18 |
PPE35 | 2168718 | p.Thr632Met | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289842 | c.-601G>T | upstream_gene_variant | 0.4 |
kasA | 2518809 | p.Lys232Arg | missense_variant | 0.5 |
folC | 2746693 | c.906G>T | synonymous_variant | 0.5 |
folC | 2747437 | p.Met54Ile | missense_variant | 1.0 |
thyX | 3068148 | c.-203A>T | upstream_gene_variant | 0.2 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449355 | p.Ser284Arg | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
alr | 3840435 | p.Leu329Gln | missense_variant | 0.4 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.33 |
alr | 3841613 | c.-193A>G | upstream_gene_variant | 0.11 |
ddn | 3986959 | p.Gly39Asp | missense_variant | 0.25 |
embC | 4241958 | p.Arg699Leu | missense_variant | 1.0 |
embC | 4242102 | p.Lys747Arg | missense_variant | 0.29 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4245587 | c.-927G>A | upstream_gene_variant | 0.29 |
embB | 4248152 | p.Ala547Thr | missense_variant | 0.14 |
embB | 4248326 | p.Ala605Thr | missense_variant | 0.11 |
embB | 4248356 | p.Ser615Pro | missense_variant | 0.12 |
embB | 4249409 | p.Pro966Ser | missense_variant | 0.13 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269344 | p.Gly164Arg | missense_variant | 0.67 |
aftB | 4269753 | c.-917G>A | upstream_gene_variant | 0.29 |
ethA | 4326855 | p.Arg207Cys | missense_variant | 0.33 |
ethA | 4328314 | c.-841G>A | upstream_gene_variant | 0.5 |
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 |