Run ID: SRR6831909
Sample name:
Date: 04-04-2023 17:06:41
Number of reads: 666393
Percentage reads mapped: 99.54
Strain: lineage2.2
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | 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 | 7773 | p.Gly158Ser | missense_variant | 0.1 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490682 | c.-101C>T | upstream_gene_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576091 | c.744C>A | synonymous_variant | 0.12 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 764664 | p.Val432Ala | missense_variant | 0.17 |
rpoC | 765035 | p.Arg556Ser | missense_variant | 0.11 |
rpoC | 765846 | p.Asn826Ile | missense_variant | 0.25 |
rpoC | 766637 | p.Lys1090* | stop_gained | 0.17 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
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 | 781487 | c.-73C>G | upstream_gene_variant | 0.22 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.15 |
fbiC | 1302811 | c.-120G>A | upstream_gene_variant | 0.13 |
fbiC | 1303493 | p.Leu188Ser | missense_variant | 0.1 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472033 | n.188A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473739 | n.82G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474309 | n.652G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474935 | n.1278A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474948 | n.1291C>T | non_coding_transcript_exon_variant | 0.17 |
inhA | 1674244 | p.Ile15Val | missense_variant | 0.11 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102995 | c.48A>T | synonymous_variant | 0.2 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154775 | p.Ser446Thr | missense_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2725945 | c.-248G>A | upstream_gene_variant | 0.22 |
pepQ | 2859410 | p.Arg337Cys | missense_variant | 0.18 |
pepQ | 2859423 | c.996C>T | synonymous_variant | 0.17 |
Rv2752c | 3065439 | c.753C>T | synonymous_variant | 0.2 |
thyA | 3073805 | p.Glu223Lys | missense_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087689 | c.870G>A | synonymous_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3613315 | c.-199T>C | upstream_gene_variant | 0.22 |
rpoA | 3877590 | c.918G>A | synonymous_variant | 0.2 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245196 | p.Ile655Thr | missense_variant | 0.5 |
embA | 4245264 | p.Asp678Tyr | missense_variant | 0.17 |
embB | 4247407 | c.894G>A | synonymous_variant | 0.18 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268906 | c.-70C>A | upstream_gene_variant | 0.33 |
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 |