Run ID: ERR2515062
Sample name:
Date: 31-03-2023 20:44:02
Number of reads: 2814892
Percentage reads mapped: 98.84
Strain: lineage2.2.1.2
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 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
lineage2.2.1.2 | East-Asian (Beijing) | Beijing-RD142 | RD105;RD207;RD181;RD142 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.25 | 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 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_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 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472655 | n.810G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472671 | n.826G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472688 | n.842_843insC | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473291 | n.1446G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475754 | n.2097G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475762 | n.2105G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475774 | n.2117C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475780 | n.2123A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475783 | n.2126T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.12 |
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 |
Rv1979c | 2223293 | c.-129A>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 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.99 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ethR | 4326763 | c.-786C>A | upstream_gene_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 |