Run ID: SRR2328057
Sample name:
Date: 04-04-2023 04:35:10
Number of reads: 1274593
Percentage reads mapped: 97.88
Strain: lineage2.2.1
Drug-resistance: Pre-XDR-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 |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Ala | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761136 | p.Thr444Pro | missense_variant | 0.31 | rifampicin |
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 | 2289096 | p.Asp49Ala | missense_variant | 1.0 | pyrazinamide |
thyX | 3067961 | c.-16C>T | upstream_gene_variant | 0.95 | para-aminosalicylic_acid |
embB | 4247730 | p.Gly406Ala | missense_variant | 1.0 | ethambutol |
thyA | 3069838 | c.-981_*3841del | transcript_ablation | 1.0 | para-aminosalicylic_acid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6307 | c.-995T>C | upstream_gene_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7567 | p.Asp89Ala | missense_variant | 0.33 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7927 | p.Asp209Ala | missense_variant | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.35 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760407 | p.Ser201Arg | missense_variant | 0.4 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764327 | p.Ile320Leu | missense_variant | 0.41 |
rpoC | 764817 | p.Val483Ala | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 778288 | p.Ser65Arg | missense_variant | 0.26 |
mmpL5 | 778480 | c.1A>G | start_lost | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304274 | p.Asp448Glu | missense_variant | 0.47 |
fbiC | 1304672 | p.Val581Gly | missense_variant | 0.29 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407039 | p.Val101Gly | missense_variant | 0.33 |
embR | 1416518 | p.Leu277Arg | missense_variant | 0.39 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471946 | n.101C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476112 | n.2455G>T | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918607 | p.Val223Gly | missense_variant | 0.45 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156552 | c.-441C>T | upstream_gene_variant | 0.95 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169063 | p.Met517Lys | missense_variant | 0.22 |
PPE35 | 2169144 | p.Val490Glu | missense_variant | 0.32 |
PPE35 | 2169909 | p.Asn235Ile | missense_variant | 0.22 |
PPE35 | 2170047 | p.Leu189Arg | missense_variant | 0.44 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyX | 3067863 | p.Asp28Ala | missense_variant | 0.26 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087183 | p.Thr122Pro | missense_variant | 0.29 |
fbiD | 3339744 | c.627A>T | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474290 | p.Glu95Ala | missense_variant | 0.25 |
fprA | 3474634 | p.Leu210Val | missense_variant | 0.36 |
whiB7 | 3568428 | c.252A>G | synonymous_variant | 0.33 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641668 | p.Val45Gly | missense_variant | 0.38 |
alr | 3840225 | p.Thr399Ile | missense_variant | 1.0 |
clpC1 | 4039063 | p.Ser548Ala | missense_variant | 0.27 |
embC | 4239868 | c.6T>G | synonymous_variant | 0.19 |
embC | 4240439 | p.Phe193Ile | missense_variant | 0.14 |
embC | 4240495 | c.633T>G | synonymous_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243192 | c.-40delT | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245457 | p.Glu742Ala | missense_variant | 0.32 |
embA | 4245640 | p.Asn803Thr | missense_variant | 0.38 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.38 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.29 |
embB | 4247219 | p.Leu236Val | missense_variant | 0.22 |
embB | 4249725 | p.Val1071Gly | missense_variant | 0.25 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267704 | p.Leu378Arg | missense_variant | 0.35 |
ethA | 4326676 | p.Ser266Arg | missense_variant | 1.0 |
whiB6 | 4338223 | p.Glu100Ala | missense_variant | 0.36 |
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 |