Run ID: ERR4820059
Sample name:
Date: 01-04-2023 16:27:29
Number of reads: 1278510
Percentage reads mapped: 93.3
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 |
---|---|---|---|---|
gyrB | 6989 | p.Asp584Asn | missense_variant | 0.1 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8056 | p.Arg252Leu | 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 | 776744 | c.1737C>G | synonymous_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475754 | n.2097G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475774 | n.2117C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.38 |
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 | 2288942 | c.300C>G | synonymous_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 |
panD | 4044059 | p.Ala75Thr | missense_variant | 0.11 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4328212 | c.-740delC | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |