Run ID: SRR8217938
Sample name:
Date: 04-04-2023 20:40:40
Number of reads: 2826850
Percentage reads mapped: 98.71
Strain: lineage2.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 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 | 576108 | p.Ala254Gly | missense_variant | 0.18 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.97 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472470 | n.625C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472697 | n.852T>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1473837 | n.180G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474751 | n.1094G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474825 | n.1168G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475961 | n.2304C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476141 | n.2484A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476506 | n.2849T>C | 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 |
fbiB | 3642576 | p.Val348Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4268619 | p.Val73Gly | missense_variant | 0.2 |
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 |