Run ID: ERR8665570
Sample name:
Date: 02-04-2023 07:32:18
Number of reads: 568726
Percentage reads mapped: 99.54
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 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
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 |
pncA | 2288836 | p.Asp136Tyr | missense_variant | 0.23 | pyrazinamide |
pncA | 2289016 | p.Thr76Pro | missense_variant | 1.0 | pyrazinamide |
embA | 4243217 | c.-16C>T | upstream_gene_variant | 1.0 | ethambutol |
embB | 4247729 | p.Gly406Cys | missense_variant | 0.29 | ethambutol |
ethA | 4326166 | c.1307dupC | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5721 | p.Gly161Val | missense_variant | 0.15 |
gyrB | 5934 | p.Ser232* | stop_gained | 0.24 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9055 | p.Pro585His | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491140 | p.Gly120Cys | missense_variant | 0.13 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575389 | c.42C>A | synonymous_variant | 0.17 |
mshA | 575787 | p.Tyr147Cys | missense_variant | 0.15 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576022 | c.675T>C | synonymous_variant | 0.25 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761049 | c.1243C>A | synonymous_variant | 0.17 |
rpoB | 761985 | p.Asp727Tyr | missense_variant | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.15 |
rpoC | 764916 | p.Leu516Pro | missense_variant | 1.0 |
rpoC | 765280 | c.1911G>T | synonymous_variant | 0.2 |
rpoC | 765297 | p.Pro643Leu | missense_variant | 0.18 |
rpoC | 765738 | p.Arg790Leu | missense_variant | 0.18 |
rpoC | 765978 | p.Ser870Tyr | missense_variant | 0.2 |
rpoC | 766314 | p.Ser982Tyr | missense_variant | 0.18 |
rpoC | 766699 | c.3330G>A | synonymous_variant | 0.12 |
rpoC | 767080 | c.3711G>T | synonymous_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777204 | p.Pro426Gln | missense_variant | 0.22 |
mmpL5 | 777215 | c.1266C>A | synonymous_variant | 0.18 |
mmpL5 | 777220 | p.Leu421Met | missense_variant | 0.18 |
mmpL5 | 777515 | p.Phe322Leu | missense_variant | 0.22 |
mmpL5 | 777885 | p.Ala199Asp | missense_variant | 0.15 |
mmpL5 | 778998 | c.-518G>C | upstream_gene_variant | 0.14 |
mmpS5 | 779564 | c.-659C>A | upstream_gene_variant | 0.12 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303330 | c.400C>A | synonymous_variant | 0.22 |
fbiC | 1303554 | c.624G>T | synonymous_variant | 0.33 |
fbiC | 1303665 | c.735G>T | synonymous_variant | 0.2 |
fbiC | 1303899 | c.969G>T | synonymous_variant | 0.2 |
fbiC | 1304032 | p.Glu368Lys | missense_variant | 0.33 |
fbiC | 1304145 | p.Trp405Cys | missense_variant | 0.33 |
fbiC | 1304814 | p.Met628Ile | missense_variant | 0.15 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406968 | p.Asp125Tyr | missense_variant | 0.2 |
Rv1258c | 1407116 | c.225G>T | synonymous_variant | 0.29 |
Rv1258c | 1407169 | p.Ala58Ser | missense_variant | 0.17 |
Rv1258c | 1407365 | c.-25G>T | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1833977 | p.Gly146Cys | missense_variant | 0.17 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.15 |
rpsA | 1834311 | p.Glu257Val | missense_variant | 0.17 |
rpsA | 1834717 | p.Phe392Leu | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918184 | p.Ala82Val | missense_variant | 0.15 |
ndh | 2101675 | c.1368G>T | synonymous_variant | 0.2 |
ndh | 2101683 | p.Gly454Cys | missense_variant | 0.2 |
ndh | 2102418 | p.Ala209Ser | missense_variant | 0.14 |
ndh | 2102875 | p.Tyr56* | stop_gained | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170571 | p.Leu14Phe | missense_variant | 0.22 |
Rv1979c | 2222688 | c.477C>A | synonymous_variant | 0.25 |
Rv1979c | 2223162 | c.3G>T | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289011 | c.231C>A | synonymous_variant | 0.2 |
pncA | 2289327 | c.-86C>G | upstream_gene_variant | 0.13 |
pncA | 2289412 | c.-171C>A | upstream_gene_variant | 0.18 |
pncA | 2289444 | c.-203T>C | upstream_gene_variant | 0.17 |
kasA | 2518237 | p.Ser41Arg | missense_variant | 0.14 |
kasA | 2518599 | p.Ala162Val | missense_variant | 0.13 |
kasA | 2519185 | c.1071C>A | synonymous_variant | 0.2 |
folC | 2747418 | p.Gln61Lys | missense_variant | 0.29 |
pepQ | 2859776 | p.Gly215Cys | missense_variant | 0.2 |
ribD | 2987195 | c.357C>A | synonymous_variant | 0.23 |
Rv2752c | 3064619 | p.Asp525Tyr | missense_variant | 0.25 |
thyX | 3067391 | c.555G>T | synonymous_variant | 0.22 |
thyX | 3067762 | p.Arg62Trp | missense_variant | 0.18 |
thyA | 3074537 | c.-66G>T | upstream_gene_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339541 | p.Asp142Tyr | missense_variant | 0.2 |
Rv3083 | 3448810 | p.Lys103Glu | missense_variant | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613037 | p.Arg27Leu | missense_variant | 0.4 |
fbiA | 3640465 | c.-77delT | upstream_gene_variant | 0.11 |
fbiA | 3640981 | p.Asp147Tyr | missense_variant | 0.17 |
fbiB | 3641639 | c.105G>T | synonymous_variant | 0.25 |
fbiB | 3641736 | p.Glu68* | stop_gained | 0.2 |
fbiB | 3642030 | p.Gly166Cys | missense_variant | 0.33 |
alr | 3840391 | p.Asp344Tyr | missense_variant | 0.25 |
alr | 3840552 | p.Gly290Val | missense_variant | 0.14 |
alr | 3840577 | p.Ala282Ser | missense_variant | 0.14 |
alr | 3841335 | p.Ser29Tyr | missense_variant | 0.18 |
rpoA | 3877569 | c.939G>T | synonymous_variant | 0.23 |
ddn | 3986742 | c.-102G>T | upstream_gene_variant | 0.17 |
ddn | 3987252 | p.Gln137Lys | missense_variant | 0.17 |
clpC1 | 4038270 | p.Pro812His | missense_variant | 0.17 |
clpC1 | 4039616 | c.1089G>T | synonymous_variant | 0.18 |
clpC1 | 4040002 | p.His235Asp | missense_variant | 0.18 |
clpC1 | 4040020 | c.685C>T | synonymous_variant | 0.15 |
clpC1 | 4040135 | c.570C>A | synonymous_variant | 0.25 |
panD | 4043891 | p.Leu131Met | missense_variant | 0.13 |
panD | 4044032 | p.Leu84Met | missense_variant | 0.18 |
embA | 4242346 | c.-887C>A | upstream_gene_variant | 0.17 |
embA | 4242481 | c.-752C>A | upstream_gene_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244756 | p.Glu508Asp | missense_variant | 0.15 |
embA | 4245990 | p.Pro920Ser | missense_variant | 0.17 |
embB | 4246940 | p.Pro143Thr | missense_variant | 0.22 |
embB | 4247626 | c.1113C>A | synonymous_variant | 0.14 |
embB | 4247933 | p.Gly474Cys | missense_variant | 0.17 |
embB | 4248946 | c.2433C>A | synonymous_variant | 0.18 |
embB | 4249254 | p.Gly914Val | missense_variant | 0.17 |
embB | 4249502 | p.Gln997Lys | missense_variant | 0.33 |
embB | 4249660 | p.Met1049Ile | missense_variant | 0.25 |
aftB | 4267329 | p.Arg503Gln | missense_variant | 0.18 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267662 | p.Ser392* | stop_gained | 0.25 |
aftB | 4268338 | p.Asp167Tyr | missense_variant | 0.22 |
ubiA | 4269707 | p.Gly43Cys | missense_variant | 0.17 |
ubiA | 4269761 | p.Gln25Lys | missense_variant | 0.18 |
ubiA | 4269990 | c.-157G>T | upstream_gene_variant | 0.33 |
ethA | 4326127 | p.Gln449His | missense_variant | 0.18 |
ethA | 4326881 | p.Gly198Val | missense_variant | 0.13 |
ethA | 4327131 | p.Arg115Gly | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407537 | c.666G>T | synonymous_variant | 0.25 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408173 | c.30G>T | synonymous_variant | 0.25 |
gid | 4408190 | p.Glu5* | stop_gained | 0.33 |