Run ID: ERR4195457
Sample name:
Date: 01-04-2023 05:18:26
Number of reads: 1008268
Percentage reads mapped: 97.36
Strain: lineage2.2.1
Drug-resistance: MDR-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 | 0.99 |
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 |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 | 575458 | c.111T>C | synonymous_variant | 0.18 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 619725 | c.-166C>T | upstream_gene_variant | 0.17 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764363 | p.Gly332Cys | missense_variant | 1.0 |
rpoC | 765341 | p.Pro658Ser | missense_variant | 0.18 |
rpoC | 767041 | c.3672G>T | synonymous_variant | 0.12 |
rpoC | 767263 | c.3895delG | frameshift_variant | 0.13 |
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 |
fbiC | 1303932 | c.1002G>T | synonymous_variant | 0.14 |
fbiC | 1304264 | p.Gly445Asp | missense_variant | 0.12 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834872 | p.Gly444Val | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918590 | c.651G>A | synonymous_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169984 | p.Ala210Val | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.14 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289082 | p.Pro54Ala | missense_variant | 1.0 |
pncA | 2289894 | c.-653G>A | upstream_gene_variant | 0.17 |
eis | 2715432 | c.-100C>T | upstream_gene_variant | 0.12 |
eis | 2715436 | c.-104G>A | upstream_gene_variant | 0.12 |
eis | 2715440 | c.-108A>C | upstream_gene_variant | 0.11 |
eis | 2715450 | c.-118T>C | upstream_gene_variant | 0.12 |
eis | 2715451 | c.-119C>A | upstream_gene_variant | 0.12 |
eis | 2715454 | c.-122T>G | upstream_gene_variant | 0.12 |
eis | 2715455 | c.-123G>A | upstream_gene_variant | 0.12 |
eis | 2715458 | c.-126T>A | upstream_gene_variant | 0.12 |
eis | 2715460 | c.-128A>G | upstream_gene_variant | 0.12 |
eis | 2715465 | c.-133G>T | upstream_gene_variant | 0.12 |
eis | 2715469 | c.-137T>C | upstream_gene_variant | 0.12 |
eis | 2715473 | c.-141A>G | upstream_gene_variant | 0.12 |
pepQ | 2859615 | c.804C>A | synonymous_variant | 0.33 |
pepQ | 2859992 | p.Leu143Val | missense_variant | 0.12 |
pepQ | 2860248 | c.171C>T | synonymous_variant | 0.11 |
Rv2752c | 3065678 | p.Lys172Glu | missense_variant | 1.0 |
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 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3612873 | p.Phe82Ile | missense_variant | 0.11 |
fbiB | 3642083 | p.Tyr183* | stop_gained | 0.11 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243702 | c.473_489delGCGCCGGGACCCTGCCG | frameshift_variant | 0.11 |
embA | 4245943 | p.Arg904His | missense_variant | 0.11 |
embB | 4246719 | p.Ala69Asp | missense_variant | 0.12 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269355 | p.Arg160Leu | missense_variant | 0.12 |
ethA | 4326713 | p.Gln254Pro | missense_variant | 1.0 |
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 |