Run ID: SRR6856126
Sample name:
Date: 04-04-2023 17:56:53
Number of reads: 430975
Percentage reads mapped: 99.62
Strain: lineage2.2.1
Drug-resistance: RR-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 |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8074 | p.Glu258Ala | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491312 | c.531delC | frameshift_variant | 0.13 |
fgd1 | 491431 | p.Ala217Thr | missense_variant | 0.25 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761019 | p.Ala405Thr | missense_variant | 0.11 |
rpoB | 762062 | p.Asp752Glu | missense_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764910 | c.1543dupA | frameshift_variant | 0.11 |
rpoC | 766967 | p.Pro1200Ser | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304414 | p.Val495Ala | missense_variant | 0.11 |
Rv1258c | 1406205 | p.Thr379Met | missense_variant | 0.11 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406821 | p.Met174Leu | missense_variant | 0.29 |
embR | 1416864 | c.483delC | frameshift_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474819 | n.1162T>A | non_coding_transcript_exon_variant | 0.1 |
fabG1 | 1673415 | c.-25C>A | upstream_gene_variant | 0.11 |
rpsA | 1833365 | c.-177G>T | upstream_gene_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168796 | p.Thr606Arg | missense_variant | 0.11 |
PPE35 | 2169995 | c.618C>T | synonymous_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289379 | c.-138T>C | upstream_gene_variant | 0.11 |
pncA | 2289558 | c.-318delT | upstream_gene_variant | 0.13 |
kasA | 2518851 | p.Met246Thr | missense_variant | 0.1 |
kasA | 2519015 | p.Ser301Ala | missense_variant | 0.11 |
eis | 2714325 | c.1008C>T | synonymous_variant | 0.15 |
eis | 2714813 | p.Glu174* | stop_gained | 0.13 |
folC | 2747406 | p.Pro65Thr | missense_variant | 0.15 |
thyX | 3067329 | p.Val206Ala | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086854 | p.Asn12Ser | missense_variant | 0.15 |
ald | 3087852 | p.Thr345Ser | missense_variant | 0.22 |
fprA | 3473988 | c.-19A>G | upstream_gene_variant | 0.11 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474233 | p.Phe76Ser | missense_variant | 0.11 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641782 | p.Val83Ala | missense_variant | 0.22 |
fbiB | 3642518 | c.984C>T | synonymous_variant | 0.13 |
clpC1 | 4038458 | c.2247G>T | synonymous_variant | 0.11 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.11 |
clpC1 | 4040894 | c.-258_-191delCAGGCGAAAGCCTGGGCGCCGGTACTTTGCCGCGTTCGCTGGCGGCGAACCGATGGCCGCTCGGCGCC | upstream_gene_variant | 0.24 |
embC | 4240805 | p.Arg315Cys | missense_variant | 0.15 |
embC | 4241978 | p.Ser706Pro | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244581 | p.Asp450Gly | missense_variant | 0.22 |
embA | 4244833 | p.Val534Ala | missense_variant | 0.15 |
embB | 4245668 | c.-846C>T | upstream_gene_variant | 0.14 |
embB | 4249020 | p.Gly836Glu | missense_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268297 | c.540A>G | synonymous_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407620 | p.Tyr195His | missense_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |