Run ID: SRR6832011
Sample name:
Date: 04-04-2023 17:10:22
Number of reads: 711072
Percentage reads mapped: 99.59
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 |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5555 | p.Gly106Ser | missense_variant | 0.15 |
gyrB | 5946 | p.Arg236Leu | missense_variant | 0.12 |
gyrB | 6746 | p.Gln503* | stop_gained | 0.18 |
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 | 576754 | c.1409_1410delGC | frameshift_variant | 0.17 |
ccsA | 620286 | c.396G>A | synonymous_variant | 0.2 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759851 | c.45G>A | synonymous_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 766355 | p.Gly996Ser | missense_variant | 0.15 |
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 | 778776 | p.Phe44Leu | missense_variant | 0.18 |
mmpR5 | 779183 | p.Gly65Val | missense_variant | 0.25 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800895 | c.87C>A | synonymous_variant | 0.25 |
rplC | 801025 | p.Ala73Thr | missense_variant | 0.14 |
fbiC | 1305316 | p.Thr796Ala | missense_variant | 0.11 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407274 | p.Asp23Asn | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473840 | n.183A>G | non_coding_transcript_exon_variant | 1.0 |
inhA | 1673883 | c.-319C>A | upstream_gene_variant | 0.2 |
inhA | 1674930 | c.729C>T | synonymous_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834344 | p.Asp268Gly | missense_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918200 | c.261G>A | synonymous_variant | 0.12 |
ndh | 2101821 | p.Lys408Glu | missense_variant | 0.2 |
ndh | 2102557 | c.486C>T | synonymous_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155083 | c.1029G>A | synonymous_variant | 0.22 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ribD | 2986758 | c.-81A>G | upstream_gene_variant | 0.22 |
Rv2752c | 3065389 | p.Arg268His | missense_variant | 0.2 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475189 | p.Cys395Arg | missense_variant | 0.11 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
panD | 4044096 | c.186C>G | synonymous_variant | 0.15 |
embC | 4239737 | c.-125_-124delAA | upstream_gene_variant | 0.14 |
embC | 4239866 | p.Ala2Ser | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244128 | p.Thr299Met | missense_variant | 0.15 |
embA | 4245699 | p.Gly823Arg | missense_variant | 0.29 |
aftB | 4267373 | c.1463delT | frameshift_variant | 0.22 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.89 |
ethA | 4326657 | p.Pro273Thr | missense_variant | 0.1 |
ethA | 4327467 | p.Glu3Lys | missense_variant | 0.5 |
ethR | 4327909 | p.Thr121Ser | missense_variant | 0.14 |
whiB6 | 4338371 | p.Thr51Pro | 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 |
gid | 4408242 | c.-40T>C | upstream_gene_variant | 0.25 |