Run ID: SRR11972429
Sample name:
Date: 03-04-2023 05:41:54
Number of reads: 222930
Percentage reads mapped: 96.33
Strain: lineage2.2
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 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 |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6636 | p.Ser466Phe | missense_variant | 0.4 |
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7513 | p.Ala71Asp | missense_variant | 0.22 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7696 | p.Ala132Asp | missense_variant | 0.17 |
gyrA | 8677 | p.Glu459Gly | missense_variant | 0.22 |
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 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 759649 | c.-158T>G | upstream_gene_variant | 0.15 |
rpoB | 759680 | c.-127G>T | upstream_gene_variant | 0.22 |
rpoB | 760378 | p.Lys191Met | missense_variant | 0.18 |
rpoB | 760562 | p.Met252Ile | missense_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764819 | p.Trp484Gly | missense_variant | 1.0 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.33 |
rpoC | 766931 | p.Ala1188Thr | missense_variant | 0.25 |
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 | 781363 | c.-197T>G | upstream_gene_variant | 0.5 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.25 |
fbiC | 1303119 | c.189G>T | synonymous_variant | 0.17 |
Rv1258c | 1406473 | p.Thr290Ser | missense_variant | 0.5 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1416552 | p.Ala266Thr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471771 | n.-75C>A | upstream_gene_variant | 0.2 |
rrl | 1474396 | n.739C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476027 | n.2370G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476101 | n.2444C>A | non_coding_transcript_exon_variant | 0.4 |
inhA | 1674556 | p.Gly119Cys | missense_variant | 0.33 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.88 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154005 | p.Glu703* | stop_gained | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169386 | c.1197_1226delGGGTACCTTCAACACGGGCGGCGCCAACAC | disruptive_inframe_deletion | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.67 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.69 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726670 | p.Glu160Lys | missense_variant | 0.25 |
ribD | 2986851 | p.Gly5Cys | missense_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612020 | p.Gly366Asp | missense_variant | 0.25 |
alr | 3841244 | c.177G>T | synonymous_variant | 0.25 |
clpC1 | 4040496 | p.Gly70Val | missense_variant | 0.15 |
embC | 4241578 | c.1716G>T | synonymous_variant | 0.5 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4246888 | c.375C>T | synonymous_variant | 0.29 |
embB | 4247533 | p.Met340Ile | missense_variant | 0.2 |
embB | 4247855 | p.Gly448Cys | missense_variant | 0.12 |
embB | 4247934 | p.Gly474Asp | missense_variant | 0.12 |
embB | 4248814 | c.2301G>A | synonymous_variant | 0.22 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268021 | c.816G>T | synonymous_variant | 0.67 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.22 |
ethR | 4326964 | c.-585G>A | upstream_gene_variant | 0.22 |
ethR | 4326970 | c.-579G>T | upstream_gene_variant | 0.22 |
ethA | 4327806 | c.-333G>T | upstream_gene_variant | 0.2 |
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 |