Run ID: ERR2513018
Sample name:
Date: 31-03-2023 19:24:28
Number of reads: 1493124
Percentage reads mapped: 97.57
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 | 0.15 | 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 | 1.0 |
gyrA | 9318 | p.Leu673Val | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575283 | c.-65C>G | upstream_gene_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.97 |
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 | 1303016 | p.Val29Gly | missense_variant | 0.19 |
embR | 1416814 | c.534G>A | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474378 | n.721G>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475102 | n.1445C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.15 |
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 | 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 |