Run ID: SRR1735641
Sample name:
Date: 27-03-2023 14:43:07
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage2.2.1
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 | 0.99 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
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 | 0.98 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.98 |
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 | 0.98 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.17 |
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 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474584 | n.927C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474673 | n.1016T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474694 | n.1037C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.16 |
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 |
folC | 2746606 | c.993C>T | synonymous_variant | 0.11 |
ald | 3086747 | c.-73A>C | 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 | 0.97 |
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 |