Run ID: SRR10869085
Sample name:
Date: 02-04-2023 19:38:36
Number of reads: 2693512
Percentage reads mapped: 50.1
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 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 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 | 0.99 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.12 |
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 | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472553 | n.708C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472572 | n.727T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472574 | n.729T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472582 | n.738_739delTA | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472594 | n.749G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472912 | n.1067C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472917 | n.1072G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472958 | n.1113A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472988 | n.1143T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476512 | n.2855C>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 | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747167 | p.Lys144Asn | missense_variant | 0.98 |
ald | 3086739 | c.-81G>A | 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 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.17 |
aftB | 4266983 | c.1854C>G | 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 | 0.99 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |