Run ID: ERR4817817
Sample name:
Date: 01-04-2023 15:12:48
Number of reads: 3815003
Percentage reads mapped: 83.5
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 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 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_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 | 778504 | c.-24G>A | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781598 | c.39G>A | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472088 | n.243T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472138 | n.293C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472147 | n.302G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472707 | n.862A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472714 | n.869A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472715 | n.870C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473191 | n.1346C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476791 | n.3134C>A | non_coding_transcript_exon_variant | 0.18 |
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 |
pncA | 2289047 | c.195C>T | synonymous_variant | 0.99 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>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 |
whiB7 | 3568857 | c.-178C>T | upstream_gene_variant | 1.0 |
panD | 4044023 | c.259C>T | synonymous_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |