Run ID: ERR4818924
Sample name:
Date: 01-04-2023 15:49:49
Number of reads: 2006652
Percentage reads mapped: 98.53
Strain: lineage2.2.1.1
Drug-resistance: Sensitive
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 |
---|
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 |
mmpL5 | 777741 | p.Val247Ala | 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 | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.13 |
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 | 2223014 | p.Tyr51Asn | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_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 | 0.98 |
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 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |