Run ID: SRR6257105
Sample name:
Date: 04-04-2023 13:26:24
Number of reads: 949108
Percentage reads mapped: 100.0
Strain: lineage2.2.1
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
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 | 0.92 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288956 | p.Lys96Gln | missense_variant | 1.0 | pyrazinamide |
eis | 2715369 | c.-37G>T | upstream_gene_variant | 1.0 | kanamycin |
folC | 2747141 | p.Glu153Ala | missense_variant | 1.0 | para-aminosalicylic_acid |
embB | 4247429 | p.Met306Val | missense_variant | 0.94 | ethambutol |
ethA | 4326669 | p.Gln269* | stop_gained | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.1 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.11 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576217 | p.Leu290Phe | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.11 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.11 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764817 | p.Val483Gly | missense_variant | 0.93 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.1 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.11 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.12 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.12 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.12 |
rpoC | 766597 | c.3228C>G | synonymous_variant | 0.1 |
rpoC | 766607 | p.Ile1080Leu | 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 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.1 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.11 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.32 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407005 | c.336G>A | synonymous_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.1 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834765 | c.1224A>G | synonymous_variant | 0.1 |
rpsA | 1834786 | c.1245A>G | synonymous_variant | 0.1 |
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 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3065002 | p.His397Arg | missense_variant | 1.0 |
ald | 3086731 | c.-89A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
rpoA | 3878559 | c.-53delC | upstream_gene_variant | 0.67 |
rpoA | 3878578 | c.-71C>A | upstream_gene_variant | 1.0 |
clpC1 | 4039364 | c.1341C>G | synonymous_variant | 0.11 |
embC | 4240642 | c.780G>C | synonymous_variant | 0.12 |
embC | 4240645 | c.783G>C | synonymous_variant | 0.11 |
embC | 4240654 | c.792C>T | synonymous_variant | 0.12 |
embC | 4240657 | c.795G>C | synonymous_variant | 0.15 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.12 |
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 |
embB | 4249323 | p.Ala937Glu | missense_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
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 |