Run ID: ERR4820471
Sample name:
Date: 01-04-2023 16:42:03
Number of reads: 1323638
Percentage reads mapped: 94.14
Strain: lineage3
Drug-resistance: Other
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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.81 | streptomycin |
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 | 0.97 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576198 | p.Leu284Gln | missense_variant | 0.13 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.33 |
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 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1305409 | p.Ala827Ser | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.29 |
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 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.18 |
Rv1979c | 2223053 | p.Glu38Lys | missense_variant | 0.97 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289326 | c.-102_-86delTGGTCATGTTCGCGATC | upstream_gene_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
thyA | 3074570 | c.-100delT | upstream_gene_variant | 0.12 |
thyA | 3074580 | c.-109T>C | upstream_gene_variant | 0.13 |
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 |