Run ID: ERR5866523
Sample name:
Date: 02-04-2023 00:44:23
Number of reads: 445864
Percentage reads mapped: 99.54
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
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 |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
katG | 2155341 | c.770delT | frameshift_variant | 0.4 | isoniazid |
katG | 2155791 | p.Trp107* | stop_gained | 0.29 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326231 | c.1242delT | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5405 | p.Glu56* | stop_gained | 0.25 |
gyrB | 6191 | p.Glu318* | stop_gained | 0.29 |
gyrB | 6322 | p.Lys361Asn | missense_variant | 0.4 |
gyrB | 6575 | p.Arg446Ser | missense_variant | 0.22 |
gyrB | 6719 | p.Asp494Tyr | missense_variant | 0.25 |
gyrB | 7169 | p.Ala644Thr | missense_variant | 0.67 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7712 | p.Leu137Phe | missense_variant | 0.22 |
gyrA | 8586 | p.Glu429* | stop_gained | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9762 | p.Glu821* | stop_gained | 0.14 |
fgd1 | 490589 | c.-194G>T | upstream_gene_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575284 | c.-64C>T | upstream_gene_variant | 0.17 |
mshA | 575591 | p.Arg82Trp | missense_variant | 0.21 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576520 | c.1176delG | frameshift_variant | 0.11 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760451 | c.645C>T | synonymous_variant | 0.33 |
rpoB | 760517 | p.Trp237Cys | missense_variant | 0.33 |
rpoB | 760663 | p.Ala286Glu | missense_variant | 0.5 |
rpoB | 761525 | p.Met573Ile | missense_variant | 0.15 |
rpoB | 761714 | c.1908C>A | synonymous_variant | 0.18 |
rpoB | 761733 | p.Val643Ile | missense_variant | 0.2 |
rpoB | 761749 | p.Ser648* | stop_gained | 0.22 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763103 | c.-267G>T | upstream_gene_variant | 0.33 |
rpoC | 764813 | p.Gln482Lys | missense_variant | 0.29 |
rpoC | 764822 | p.Asp485Tyr | missense_variant | 1.0 |
rpoC | 766144 | c.2775G>A | synonymous_variant | 0.29 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
rpoC | 766899 | p.Pro1177His | missense_variant | 0.29 |
rpoC | 767128 | c.3759C>T | synonymous_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775754 | c.2727C>A | synonymous_variant | 0.2 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpR5 | 778178 | c.-812G>A | upstream_gene_variant | 0.15 |
mmpR5 | 778346 | c.-644G>T | upstream_gene_variant | 0.33 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801101 | p.Gly98Val | missense_variant | 0.29 |
fbiC | 1303010 | p.Arg27Leu | missense_variant | 0.17 |
fbiC | 1305009 | c.2079C>A | synonymous_variant | 0.33 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406885 | c.456G>T | synonymous_variant | 0.2 |
Rv1258c | 1407022 | p.Ala107Ser | missense_variant | 0.14 |
Rv1258c | 1407492 | c.-152C>A | upstream_gene_variant | 0.13 |
embR | 1416778 | c.570G>T | synonymous_variant | 0.18 |
embR | 1417249 | c.99C>A | synonymous_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476733 | n.3076C>A | non_coding_transcript_exon_variant | 0.67 |
fabG1 | 1673151 | c.-289C>A | upstream_gene_variant | 0.17 |
fabG1 | 1674137 | p.Ser233Tyr | missense_variant | 0.33 |
rpsA | 1833959 | p.Leu140Ile | missense_variant | 0.33 |
rpsA | 1834118 | p.Gln193Lys | missense_variant | 0.33 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918734 | p.Ser265Arg | missense_variant | 0.5 |
ndh | 2103040 | c.3G>T | start_lost | 0.5 |
ndh | 2103113 | c.-71C>T | upstream_gene_variant | 0.29 |
katG | 2153969 | p.Asp715Tyr | missense_variant | 0.18 |
katG | 2154051 | c.2061G>T | synonymous_variant | 0.2 |
katG | 2154238 | p.Thr625Lys | missense_variant | 0.4 |
katG | 2154703 | p.Ser470* | stop_gained | 0.67 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2156012 | p.Gly34* | stop_gained | 0.29 |
PPE35 | 2167708 | p.Gly969Cys | missense_variant | 0.29 |
PPE35 | 2168442 | p.Trp724Leu | missense_variant | 0.18 |
PPE35 | 2168545 | p.Gly690Trp | missense_variant | 0.67 |
PPE35 | 2170704 | c.-92C>A | upstream_gene_variant | 0.2 |
PPE35 | 2170707 | c.-95G>T | upstream_gene_variant | 0.18 |
Rv1979c | 2221747 | p.Arg473Leu | missense_variant | 0.33 |
Rv1979c | 2222809 | p.Arg119Leu | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289933 | c.-692G>T | upstream_gene_variant | 0.4 |
eis | 2715278 | p.Leu19Met | missense_variant | 0.17 |
eis | 2715411 | c.-79A>G | upstream_gene_variant | 0.15 |
ribD | 2987200 | p.Thr121Asn | missense_variant | 0.18 |
Rv2752c | 3064699 | p.Ser498Tyr | missense_variant | 0.67 |
Rv2752c | 3065729 | p.Ala155Thr | missense_variant | 0.25 |
Rv2752c | 3066303 | c.-112C>A | upstream_gene_variant | 0.33 |
thyA | 3073701 | c.771C>A | synonymous_variant | 0.25 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087341 | c.522C>A | synonymous_variant | 0.18 |
ald | 3087820 | p.Arg334Leu | missense_variant | 0.2 |
fbiD | 3339435 | c.318G>T | synonymous_variant | 0.13 |
Rv3083 | 3448656 | c.153G>A | synonymous_variant | 0.18 |
fprA | 3474928 | p.Gly308Cys | missense_variant | 0.17 |
fprA | 3475113 | c.1107G>T | synonymous_variant | 0.17 |
whiB7 | 3568572 | c.108C>A | synonymous_variant | 0.25 |
Rv3236c | 3612469 | p.Glu216Asp | missense_variant | 0.33 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3641230 | p.Arg230Ser | missense_variant | 0.22 |
fbiB | 3641640 | p.Ala36* | stop_gained | 0.15 |
ddn | 3986982 | p.Ala47Thr | missense_variant | 0.33 |
clpC1 | 4040109 | p.Arg199Gln | missense_variant | 0.29 |
clpC1 | 4040301 | p.Arg135His | missense_variant | 0.25 |
clpC1 | 4040507 | c.198C>A | synonymous_variant | 0.17 |
panD | 4044259 | p.Ser8* | stop_gained | 0.2 |
embC | 4240737 | p.Ser292Tyr | missense_variant | 0.15 |
embC | 4241035 | c.1173G>T | synonymous_variant | 0.18 |
embC | 4241397 | p.Trp512Leu | missense_variant | 0.22 |
embC | 4241457 | p.Ala532Asp | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242750 | p.Pro963Gln | missense_variant | 0.18 |
embA | 4243299 | p.Ala23Ser | missense_variant | 0.29 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244068 | p.Thr279Ile | missense_variant | 0.18 |
embA | 4245091 | p.Gly620Val | missense_variant | 0.22 |
embB | 4246181 | c.-333C>A | upstream_gene_variant | 0.14 |
embB | 4248883 | c.2370C>A | synonymous_variant | 0.2 |
embB | 4249452 | p.Ser980* | stop_gained | 0.2 |
embB | 4249495 | p.Phe994Leu | missense_variant | 0.25 |
embB | 4249543 | c.3030G>A | synonymous_variant | 0.4 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268273 | c.564A>G | synonymous_variant | 0.18 |
aftB | 4268746 | p.Gly31Arg | missense_variant | 0.25 |
ubiA | 4269896 | c.-63G>A | upstream_gene_variant | 0.13 |
ethA | 4326033 | p.Ala481Thr | missense_variant | 0.22 |
ethA | 4326099 | p.Gln459Lys | missense_variant | 0.25 |
ethA | 4326333 | p.Ala381Ser | missense_variant | 0.33 |
ethR | 4326670 | c.-879G>T | upstream_gene_variant | 0.5 |
ethA | 4327671 | c.-198C>A | upstream_gene_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407810 | c.393C>T | synonymous_variant | 0.29 |
gid | 4407927 | p.Glu92Asp | missense_variant | 0.67 |