Run ID: SRR11972266
Sample name:
Date: 03-04-2023 05:34:10
Number of reads: 370351
Percentage reads mapped: 99.51
Strain: lineage2.2.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.98 |
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8485 | p.Val395Ala | missense_variant | 0.17 |
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 | 576503 | c.1158delC | frameshift_variant | 0.22 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761379 | p.Leu525Val | missense_variant | 0.33 |
rpoB | 761530 | p.Val575Gly | missense_variant | 0.12 |
rpoB | 761674 | p.Gly623Glu | missense_variant | 0.12 |
rpoB | 762516 | p.Gly904Ser | missense_variant | 0.12 |
rpoB | 762536 | p.Ile910Met | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763220 | c.-150G>C | upstream_gene_variant | 0.13 |
rpoC | 766342 | c.2973C>A | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775692 | p.Ala930Val | missense_variant | 0.12 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776507 | c.1974C>G | synonymous_variant | 0.13 |
mmpL5 | 776976 | p.Ser502Asn | missense_variant | 0.15 |
mmpL5 | 777951 | p.Ala177Val | missense_variant | 0.12 |
mmpR5 | 779159 | p.Ala57Val | missense_variant | 0.15 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305322 | p.Val798Leu | missense_variant | 0.13 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461105 | p.Ala21Thr | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1674026 | p.Glu196Gly | missense_variant | 0.29 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.95 |
rpsA | 1834917 | p.Thr459Ile | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918628 | p.Leu230Pro | missense_variant | 0.17 |
ndh | 2102073 | p.Ala324Ser | missense_variant | 0.12 |
katG | 2153909 | p.Asp735His | missense_variant | 0.17 |
katG | 2153972 | p.Asp714Asn | missense_variant | 0.14 |
katG | 2153988 | c.2124C>T | synonymous_variant | 0.14 |
katG | 2154210 | c.1902C>T | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155603 | p.Asn170Ser | missense_variant | 0.29 |
katG | 2155607 | p.Gly169Ser | missense_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168249 | c.2364G>A | synonymous_variant | 0.17 |
PPE35 | 2168327 | c.2286G>A | synonymous_variant | 0.14 |
Rv1979c | 2222117 | p.Met350Leu | missense_variant | 0.17 |
Rv1979c | 2223147 | c.18G>A | synonymous_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289897 | c.-656G>A | upstream_gene_variant | 0.22 |
pncA | 2290214 | c.-973T>C | upstream_gene_variant | 0.14 |
kasA | 2518018 | c.-97A>G | upstream_gene_variant | 0.25 |
kasA | 2518406 | p.Ala98Thr | missense_variant | 0.13 |
eis | 2715042 | c.291G>A | synonymous_variant | 0.12 |
eis | 2715066 | c.267G>A | synonymous_variant | 0.12 |
ahpC | 2726447 | c.255T>G | synonymous_variant | 0.15 |
Rv2752c | 3064689 | c.1503C>T | synonymous_variant | 1.0 |
Rv2752c | 3065169 | c.1023C>A | synonymous_variant | 0.2 |
Rv2752c | 3065694 | c.498G>A | synonymous_variant | 0.13 |
Rv2752c | 3065970 | c.222C>T | synonymous_variant | 0.18 |
thyX | 3067966 | c.-21G>A | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087067 | p.Gly83Asp | missense_variant | 0.17 |
ald | 3087116 | c.297G>T | synonymous_variant | 0.13 |
Rv3083 | 3448404 | c.-100C>T | upstream_gene_variant | 0.15 |
Rv3083 | 3449668 | p.Gly389Cys | missense_variant | 0.17 |
fprA | 3473986 | c.-21G>A | upstream_gene_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474719 | p.Ala238Glu | missense_variant | 0.12 |
Rv3236c | 3612760 | c.357C>A | synonymous_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641255 | p.Ala238Val | missense_variant | 0.33 |
fbiB | 3642312 | p.Arg260Cys | missense_variant | 0.22 |
ddn | 3986765 | c.-79T>C | upstream_gene_variant | 0.14 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.14 |
embC | 4240759 | c.897C>T | synonymous_variant | 0.15 |
embC | 4242144 | p.Pro761Leu | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245124 | p.Gly631Glu | missense_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.85 |
ethR | 4328128 | p.Val194Met | missense_variant | 0.18 |
whiB6 | 4338473 | p.Arg17Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407644 | p.Arg187Trp | missense_variant | 0.13 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408059 | p.His48Gln | missense_variant | 0.12 |