Run ID: SRR21277770
Sample name:
Date: 04-04-2023 01:40:39
Number of reads: 14535144
Percentage reads mapped: 98.09
Strain: lineage2.2.1.1
Drug-resistance: Other
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 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | streptomycin |
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 | 491295 | c.513C>A | synonymous_variant | 0.11 |
fgd1 | 491311 | p.Gly177Arg | missense_variant | 0.12 |
fgd1 | 491321 | p.Ala180Val | missense_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575494 | c.147G>T | synonymous_variant | 0.15 |
mshA | 575499 | p.Ala51Val | missense_variant | 0.15 |
mshA | 575870 | p.His175Asn | missense_variant | 0.29 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576457 | c.1110G>A | synonymous_variant | 0.17 |
mshA | 576602 | c.1255C>A | synonymous_variant | 0.5 |
ccsA | 620135 | p.Ala82Val | missense_variant | 0.13 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 762776 | c.-594C>T | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763933 | c.564C>A | synonymous_variant | 0.14 |
rpoC | 764579 | p.Asp404Tyr | missense_variant | 0.14 |
rpoC | 766048 | c.2679C>A | synonymous_variant | 0.11 |
rpoC | 766106 | p.Asp913Tyr | missense_variant | 0.12 |
rpoC | 766969 | c.3600C>A | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.99 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 779355 | c.-875C>A | upstream_gene_variant | 0.11 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801245 | p.Arg146His | missense_variant | 0.19 |
rplC | 801252 | c.444G>T | synonymous_variant | 0.11 |
fbiC | 1303104 | c.174G>A | synonymous_variant | 0.12 |
fbiC | 1303107 | p.Cys59* | stop_gained | 0.11 |
fbiC | 1303114 | p.Ala62Thr | missense_variant | 0.2 |
fbiC | 1303935 | c.1005G>T | synonymous_variant | 0.13 |
fbiC | 1304261 | p.Trp444Leu | missense_variant | 0.1 |
fbiC | 1305452 | p.Gly841Asp | missense_variant | 0.19 |
fbiC | 1305456 | c.2526C>A | synonymous_variant | 0.1 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406964 | p.Ser126Leu | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834869 | p.Arg443His | missense_variant | 0.12 |
tlyA | 1917955 | p.Arg6Ser | missense_variant | 0.17 |
tlyA | 1917970 | p.Leu11Met | missense_variant | 0.22 |
tlyA | 1918059 | c.120C>T | synonymous_variant | 0.12 |
tlyA | 1918176 | c.237C>A | synonymous_variant | 0.15 |
tlyA | 1918191 | c.252G>T | synonymous_variant | 0.17 |
tlyA | 1918252 | p.Ala105Ser | missense_variant | 0.11 |
tlyA | 1918566 | c.627C>A | synonymous_variant | 0.27 |
tlyA | 1918588 | p.Glu217* | stop_gained | 0.19 |
tlyA | 1918602 | c.663C>T | synonymous_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155757 | p.Arg119Ser | missense_variant | 0.15 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168788 | p.Thr609Ala | missense_variant | 0.38 |
PPE35 | 2170037 | c.576C>T | synonymous_variant | 0.23 |
PPE35 | 2170103 | c.510C>A | synonymous_variant | 0.11 |
PPE35 | 2170446 | p.Ser56* | stop_gained | 0.11 |
Rv1979c | 2223062 | p.Thr35Ala | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519047 | p.His311Gln | missense_variant | 0.14 |
eis | 2714846 | p.Val163Ile | missense_variant | 1.0 |
eis | 2715045 | c.288G>A | synonymous_variant | 0.67 |
folC | 2746342 | c.1257G>A | synonymous_variant | 0.14 |
folC | 2746347 | p.Ala418Thr | missense_variant | 0.13 |
folC | 2746577 | p.Arg341Leu | missense_variant | 0.11 |
folC | 2747715 | c.-117G>T | upstream_gene_variant | 0.11 |
pepQ | 2859600 | c.819G>T | synonymous_variant | 0.11 |
pepQ | 2859603 | p.Gly272Cys | missense_variant | 0.1 |
pepQ | 2859610 | p.Leu270Gln | missense_variant | 0.11 |
pepQ | 2859919 | p.Arg167Leu | missense_variant | 0.13 |
pepQ | 2859941 | p.Arg160Ser | missense_variant | 0.25 |
pepQ | 2859954 | c.465C>A | synonymous_variant | 0.15 |
pepQ | 2860583 | c.-165G>T | upstream_gene_variant | 0.14 |
pepQ | 2860589 | c.-171G>T | upstream_gene_variant | 0.64 |
ribD | 2986647 | c.-192G>T | upstream_gene_variant | 0.11 |
ribD | 2987306 | c.468C>A | synonymous_variant | 0.2 |
Rv2752c | 3066297 | c.-106G>A | upstream_gene_variant | 0.11 |
thyX | 3067300 | p.Leu216Met | missense_variant | 0.18 |
thyX | 3067302 | p.Cys215Phe | missense_variant | 0.1 |
thyX | 3067541 | p.Ala135Glu | missense_variant | 0.2 |
thyX | 3067856 | c.90C>T | synonymous_variant | 0.12 |
thyX | 3068001 | c.-56G>T | upstream_gene_variant | 0.13 |
thyA | 3074198 | p.Pro92Ser | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087296 | c.477G>A | synonymous_variant | 0.12 |
fbiD | 3339319 | p.Ala68Thr | missense_variant | 0.11 |
fbiD | 3339339 | c.222G>T | synonymous_variant | 0.21 |
fbiD | 3339436 | p.Ala107Thr | missense_variant | 1.0 |
fbiD | 3339561 | c.444C>A | synonymous_variant | 0.19 |
fbiD | 3339746 | p.Ala210Val | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474928 | p.Gly308Ser | missense_variant | 0.12 |
fprA | 3474981 | c.975C>T | synonymous_variant | 0.18 |
fprA | 3474987 | c.981G>T | synonymous_variant | 0.12 |
fprA | 3475309 | p.Glu435* | stop_gained | 0.11 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.99 |
fbiB | 3641625 | p.Ala31Thr | missense_variant | 0.11 |
fbiB | 3641903 | c.369C>A | synonymous_variant | 0.11 |
fbiB | 3642029 | c.495C>T | synonymous_variant | 0.11 |
fbiB | 3642273 | p.Glu247* | stop_gained | 0.17 |
fbiB | 3642382 | p.Ala283Val | missense_variant | 0.11 |
fbiB | 3642394 | p.Pro287Leu | missense_variant | 0.11 |
alr | 3841471 | c.-51A>T | upstream_gene_variant | 0.21 |
embC | 4241253 | p.Ser464Phe | missense_variant | 0.11 |
embC | 4241689 | c.1827G>A | synonymous_variant | 0.19 |
embC | 4242371 | p.Ala837Thr | missense_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242725 | p.Gln955* | stop_gained | 0.11 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243478 | c.246G>A | synonymous_variant | 0.11 |
embA | 4243616 | c.384C>T | synonymous_variant | 0.17 |
embA | 4243905 | p.Asp225Asn | missense_variant | 0.11 |
embA | 4243947 | p.Arg239* | stop_gained | 0.11 |
embA | 4244210 | c.978G>A | synonymous_variant | 0.13 |
embA | 4244213 | c.981C>A | synonymous_variant | 0.12 |
embA | 4244438 | c.1206C>A | synonymous_variant | 0.17 |
embA | 4244443 | p.Arg404Gln | missense_variant | 0.11 |
embA | 4244446 | p.Leu405Gln | missense_variant | 0.17 |
embA | 4244597 | c.1365G>T | synonymous_variant | 0.21 |
embA | 4244606 | c.1374G>T | synonymous_variant | 0.13 |
embA | 4244848 | p.Gly539Asp | missense_variant | 0.1 |
embA | 4244864 | c.1632G>A | synonymous_variant | 0.14 |
embA | 4245669 | p.Ala813Thr | missense_variant | 0.1 |
embA | 4245772 | p.Asn847Ser | missense_variant | 1.0 |
embB | 4246654 | c.141G>A | synonymous_variant | 0.17 |
embB | 4246688 | p.Pro59Thr | missense_variant | 0.14 |
embB | 4247123 | p.Ala204Ser | missense_variant | 0.12 |
embB | 4247863 | c.1350C>A | synonymous_variant | 0.19 |
embB | 4247869 | c.1356G>A | synonymous_variant | 0.18 |
embB | 4247870 | p.Ala453Thr | missense_variant | 0.29 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
embB | 4248593 | p.Gly694Ser | missense_variant | 0.12 |
embB | 4248597 | p.Glu695Val | missense_variant | 0.12 |
embB | 4248603 | p.Arg697Leu | missense_variant | 0.11 |
embB | 4249119 | p.Asp869Gly | missense_variant | 1.0 |
aftB | 4267622 | c.1215G>T | synonymous_variant | 0.1 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.91 |
aftB | 4267676 | c.1161G>A | synonymous_variant | 0.11 |
aftB | 4267931 | c.906C>T | synonymous_variant | 0.17 |
aftB | 4267955 | c.882G>A | synonymous_variant | 0.16 |
aftB | 4267969 | p.Leu290Met | missense_variant | 0.12 |
ubiA | 4269714 | p.Leu40Phe | missense_variant | 0.11 |
ethR | 4328032 | p.Ala162Thr | missense_variant | 0.11 |
ethA | 4328037 | c.-564C>T | upstream_gene_variant | 0.11 |
ethA | 4328433 | c.-960G>T | upstream_gene_variant | 0.12 |
whiB6 | 4338320 | p.Glu68* | stop_gained | 0.13 |
whiB6 | 4338326 | p.Ala66Thr | missense_variant | 0.1 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.99 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |