Run ID: ERR4815077
Sample name:
Date: 01-04-2023 13:39:34
Number of reads: 2189855
Percentage reads mapped: 99.35
Strain: lineage2.2.1.1
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 |
lineage2.2.1.1 | East-Asian (Beijing) | Beijing-RD150 | RD105;RD207;RD181;RD150 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781822 | p.Lys88Arg | 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 | 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 |
fbiC | 1304850 | p.Asn640Lys | missense_variant | 0.5 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472274 | n.429A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473279 | n.1434G>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473346 | n.1501G>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473365 | n.1520C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476027 | n.2373delA | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.11 |
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 | 2170048 | p.Leu189Val | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518871 | p.His253Tyr | missense_variant | 1.0 |
eis | 2714846 | p.Val163Ile | missense_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 | 1.0 |
embB | 4248115 | c.1602C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338600 | c.-79T>G | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |