Run ID: ERR2027291
Sample name:
Date: 31-03-2023 15:42:27
Number of reads: 2080627
Percentage reads mapped: 89.95
Strain: lineage3.1.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1.3 | 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 |
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 | 1.0 |
Rv1258c | 1406613 | p.Glu243Ala | missense_variant | 0.98 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472092 | n.247C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476306 | n.2649A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476307 | n.2650A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1834159 | c.618G>A | 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 | 2222732 | c.432delT | frameshift_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
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 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249195 | c.2682C>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4408175 | p.Ala10Pro | missense_variant | 1.0 |