Run ID: SRR11972462
Sample name:
Date: 03-04-2023 05:43:50
Number of reads: 636330
Percentage reads mapped: 98.22
Strain: lineage2.2.1
Drug-resistance: Sensitive
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 | 0.98 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5312 | p.Ala25Thr | missense_variant | 0.12 |
gyrB | 5727 | p.Pro163Gln | missense_variant | 0.18 |
gyrB | 5825 | p.Glu196* | stop_gained | 0.12 |
gyrB | 6078 | p.Gly280Val | missense_variant | 0.2 |
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 | 491718 | c.936A>T | synonymous_variant | 0.22 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575442 | p.Gly32Glu | missense_variant | 0.22 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620865 | c.975A>G | stop_lost&splice_region_variant | 0.17 |
rpoB | 761680 | p.Glu625Gly | missense_variant | 0.4 |
rpoB | 761981 | c.2175C>T | synonymous_variant | 0.2 |
rpoB | 762086 | c.2280G>A | synonymous_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.15 |
rpoC | 765365 | p.Thr666Ala | missense_variant | 0.5 |
rpoC | 766316 | p.Met983Val | missense_variant | 0.18 |
rpoC | 767126 | p.Ile1253Val | missense_variant | 0.22 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775715 | c.2766G>A | synonymous_variant | 0.15 |
mmpL5 | 775718 | c.2763C>G | synonymous_variant | 0.17 |
mmpL5 | 775726 | c.2755C>T | synonymous_variant | 0.17 |
mmpL5 | 775727 | c.2754C>G | synonymous_variant | 0.17 |
mmpL5 | 775751 | c.2730C>T | synonymous_variant | 0.13 |
mmpL5 | 776010 | c.2470delC | frameshift_variant | 0.2 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 777572 | c.909C>T | synonymous_variant | 0.18 |
mmpL5 | 778303 | p.Gln60Lys | missense_variant | 0.15 |
mmpS5 | 778884 | p.Ala8Ser | missense_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.89 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303280 | p.Gln117Arg | missense_variant | 0.11 |
fbiC | 1304758 | p.Pro610Ser | missense_variant | 0.15 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
embR | 1417466 | c.-119T>C | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917833 | c.-107G>T | upstream_gene_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101790 | p.Thr418Met | missense_variant | 0.2 |
ndh | 2102155 | c.888G>A | synonymous_variant | 0.25 |
katG | 2154567 | c.1545C>A | synonymous_variant | 0.18 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167833 | p.Leu927Arg | missense_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167955 | c.2658A>C | synonymous_variant | 0.14 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.15 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.19 |
PPE35 | 2170808 | c.-196G>A | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714526 | c.805_806delAC | frameshift_variant | 1.0 |
eis | 2715057 | c.276C>T | synonymous_variant | 0.17 |
eis | 2715060 | p.His91Met | missense_variant | 0.18 |
eis | 2715065 | p.Thr90Ala | missense_variant | 0.18 |
folC | 2746887 | p.Val238Ile | missense_variant | 0.25 |
pepQ | 2860595 | c.-179_-178delAC | upstream_gene_variant | 0.13 |
Rv2752c | 3065073 | c.1119C>T | synonymous_variant | 0.14 |
Rv2752c | 3065498 | p.Arg232Trp | missense_variant | 0.13 |
Rv2752c | 3065711 | p.Gly161Ser | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474498 | c.492G>A | synonymous_variant | 0.12 |
Rv3236c | 3612734 | p.Ser128Tyr | missense_variant | 0.29 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641451 | c.-84G>T | upstream_gene_variant | 0.17 |
fbiA | 3641504 | p.Arg321His | missense_variant | 1.0 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.17 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.12 |
clpC1 | 4039829 | p.Leu292Ile | missense_variant | 0.13 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243054 | c.-179G>T | upstream_gene_variant | 0.25 |
embA | 4243206 | c.-27T>A | upstream_gene_variant | 0.2 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244447 | c.1215G>T | synonymous_variant | 0.2 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.22 |
embB | 4247472 | p.Phe320Tyr | missense_variant | 0.22 |
embB | 4248834 | p.Trp774* | stop_gained | 0.13 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268680 | p.Glu53Lys | missense_variant | 0.29 |
ubiA | 4269922 | c.-89C>T | upstream_gene_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |