Run ID: ERR1199087
Sample name:
Date: 15-08-2022 10:09:16
Number of reads: 4206129
Percentage reads mapped: 88.54
Strain: lineage4.6.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.1 | Euro-American (Uganda) | T2 | RD724 | 1.0 |
lineage4.6.1.1 | Euro-American | T2-Uganda | RD724 | 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 | 7539 | p.Thr80Ala | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472333 | n.488G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472349 | n.504A>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472374 | n.529T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472911 | n.1066T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472915 | n.1070G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472918 | n.1073A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473206 | n.1361G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473353 | n.1508C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474848 | n.1191G>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1474851 | n.1194T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476408 | n.2751G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476413 | n.2756A>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476414 | n.2757T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476543 | n.2886G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476567 | n.2910C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476573 | n.2916A>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.18 |
inhA | 1674837 | c.636C>A | synonymous_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169866 | c.747G>C | synonymous_variant | 0.16 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.21 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4328329 | c.-856C>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |