Run ID: ERR4818484
Sample name:
Date: 01-04-2023 15:35:11
Number of reads: 2236877
Percentage reads mapped: 99.43
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 | 0.99 |
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 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472958 | n.1113A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472959 | n.1114T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472963 | n.1118G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472987 | n.1142G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472988 | n.1143T>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473001 | n.1156G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473008 | n.1163C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474043 | n.386G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475756 | n.2101_2108delACCCGCAA | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.43 |
inhA | 1673460 | c.-742A>C | upstream_gene_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 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.99 |
Rv2752c | 3066160 | p.Leu11Arg | missense_variant | 1.0 |
thyX | 3068151 | c.-206T>C | upstream_gene_variant | 0.99 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
alr | 3841473 | c.-53G>A | upstream_gene_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 |