Run ID: ERR8665587
Sample name:
Date: 02-04-2023 07:32:55
Number of reads: 502516
Percentage reads mapped: 99.55
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 | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
tlyA | 1918517 | c.582delC | frameshift_variant | 1.0 | capreomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288756 | c.484_485dupGG | frameshift_variant | 1.0 | pyrazinamide |
pncA | 2288954 | p.Lys96Asn | missense_variant | 0.43 | pyrazinamide |
embB | 4248003 | p.Gln497Arg | missense_variant | 0.94 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7030 | c.-272C>A | upstream_gene_variant | 0.15 |
gyrA | 7313 | c.12G>T | synonymous_variant | 0.29 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8400 | p.Asp367Tyr | missense_variant | 0.2 |
gyrA | 8831 | p.Leu510Phe | missense_variant | 0.33 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9571 | p.Arg757Leu | missense_variant | 0.17 |
gyrA | 9582 | p.Arg761Trp | missense_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575369 | p.Asp8Tyr | missense_variant | 0.22 |
mshA | 575743 | p.Phe132Leu | missense_variant | 0.25 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 575910 | p.Leu188Pro | missense_variant | 0.22 |
ccsA | 619850 | c.-41G>T | upstream_gene_variant | 0.33 |
ccsA | 620427 | c.537C>A | synonymous_variant | 0.17 |
ccsA | 620619 | c.729G>T | synonymous_variant | 0.33 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760420 | p.Trp205Leu | missense_variant | 0.2 |
rpoB | 761567 | p.Met587Ile | missense_variant | 0.18 |
rpoB | 761689 | p.Ala628Glu | missense_variant | 0.18 |
rpoB | 762477 | p.Lys891Glu | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764185 | c.816C>A | synonymous_variant | 0.2 |
rpoC | 764839 | c.1470C>A | synonymous_variant | 0.18 |
rpoC | 765413 | p.Pro682Thr | missense_variant | 0.2 |
rpoC | 765820 | c.2451G>T | synonymous_variant | 0.25 |
rpoC | 766252 | p.Lys961Asn | missense_variant | 0.13 |
rpoC | 766459 | c.3090G>T | synonymous_variant | 0.18 |
rpoC | 767237 | p.Asp1290Asn | missense_variant | 0.13 |
mmpL5 | 775587 | c.2894G>T | stop_lost&splice_region_variant | 0.5 |
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 | 777211 | p.Asp424Tyr | missense_variant | 0.17 |
mmpR5 | 779258 | p.Arg90Leu | missense_variant | 0.29 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781607 | c.48C>A | synonymous_variant | 0.15 |
rpsL | 781635 | p.Gly26Arg | missense_variant | 0.13 |
fbiC | 1304810 | p.Ser627Tyr | missense_variant | 0.17 |
Rv1258c | 1406104 | c.1237C>A | synonymous_variant | 0.2 |
Rv1258c | 1406402 | c.939C>A | synonymous_variant | 0.17 |
Rv1258c | 1406660 | c.681C>A | synonymous_variant | 0.29 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407386 | c.-46C>A | upstream_gene_variant | 0.2 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476248 | n.2591G>T | non_coding_transcript_exon_variant | 0.18 |
inhA | 1674726 | c.525G>T | synonymous_variant | 0.22 |
rpsA | 1833515 | c.-27C>A | upstream_gene_variant | 0.18 |
rpsA | 1833950 | p.Gly137Cys | missense_variant | 0.18 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917947 | p.Arg3Leu | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102727 | p.His106Asn | missense_variant | 0.23 |
ndh | 2103074 | c.-32C>G | upstream_gene_variant | 0.1 |
katG | 2154626 | p.Arg496Ser | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154941 | p.Glu391* | stop_gained | 0.29 |
katG | 2155017 | c.1095G>T | synonymous_variant | 0.15 |
katG | 2155173 | c.939C>A | synonymous_variant | 0.2 |
katG | 2155275 | c.837C>A | synonymous_variant | 0.17 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169866 | c.747G>T | synonymous_variant | 0.17 |
Rv1979c | 2222232 | c.933G>T | synonymous_variant | 0.2 |
Rv1979c | 2223250 | c.-86C>A | upstream_gene_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289709 | c.-468G>T | upstream_gene_variant | 0.33 |
kasA | 2518330 | p.Met72Ile | missense_variant | 0.25 |
eis | 2714825 | p.Glu170* | stop_gained | 0.18 |
ahpC | 2726037 | c.-156G>T | upstream_gene_variant | 0.17 |
ribD | 2987466 | p.Glu210* | stop_gained | 0.4 |
ribD | 2987515 | p.Arg226His | missense_variant | 0.33 |
Rv2752c | 3065235 | c.957G>T | synonymous_variant | 0.2 |
Rv2752c | 3065453 | p.Gln247* | stop_gained | 1.0 |
Rv2752c | 3067130 | c.-939G>T | upstream_gene_variant | 0.14 |
thyA | 3073832 | p.Glu214* | stop_gained | 0.23 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 0.14 |
fbiD | 3339294 | c.177C>A | synonymous_variant | 0.18 |
fbiD | 3339470 | p.Pro118Gln | missense_variant | 0.25 |
Rv3083 | 3449109 | c.606C>A | synonymous_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474670 | p.Asp222Tyr | missense_variant | 0.25 |
fprA | 3474775 | p.Asp257Tyr | missense_variant | 0.29 |
fprA | 3474794 | p.Gly263Val | missense_variant | 0.25 |
whiB7 | 3568521 | p.Leu53Phe | missense_variant | 0.17 |
whiB7 | 3568735 | c.-56G>T | upstream_gene_variant | 0.15 |
whiB7 | 3568736 | c.-57T>G | upstream_gene_variant | 1.0 |
Rv3236c | 3612270 | p.Asp283Tyr | missense_variant | 0.33 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641196 | c.-339C>A | upstream_gene_variant | 0.2 |
rpoA | 3878423 | p.Gly29* | stop_gained | 0.14 |
ddn | 3986877 | p.Pro12Ser | missense_variant | 0.15 |
clpC1 | 4038234 | p.Arg824Pro | missense_variant | 0.18 |
clpC1 | 4039917 | p.Gly263Val | missense_variant | 0.25 |
clpC1 | 4039926 | p.Arg260Leu | missense_variant | 0.25 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.18 |
clpC1 | 4040521 | p.Gln62Lys | missense_variant | 0.18 |
panD | 4044122 | c.160C>A | synonymous_variant | 0.2 |
panD | 4044436 | c.-155C>A | upstream_gene_variant | 0.18 |
panD | 4044437 | c.-156C>T | upstream_gene_variant | 0.18 |
embA | 4242352 | c.-881G>T | upstream_gene_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243346 | c.114A>G | synonymous_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243586 | p.Phe118Leu | missense_variant | 0.25 |
embA | 4243631 | c.399G>T | synonymous_variant | 0.29 |
embA | 4244201 | p.Trp323Cys | missense_variant | 0.33 |
embA | 4244231 | c.999C>A | synonymous_variant | 0.4 |
embA | 4245982 | p.Gly917Val | missense_variant | 0.33 |
embB | 4249652 | p.His1047Asn | missense_variant | 0.15 |
embB | 4249797 | p.Arg1095Leu | missense_variant | 0.27 |
aftB | 4267088 | c.1749C>A | synonymous_variant | 0.29 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268201 | c.636G>T | synonymous_variant | 0.27 |
ethA | 4326851 | p.Ser208Leu | missense_variant | 1.0 |
ethA | 4326927 | p.Ser183Arg | missense_variant | 0.42 |
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 |