Run ID: ERR405223
Sample name:
Date: 01-04-2023 04:30:19
Number of reads: 4358970
Percentage reads mapped: 86.46
Strain: lineage4.6.1.2
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 | 0.99 |
lineage4.6.1 | Euro-American (Uganda) | T2 | RD724 | 0.99 |
lineage4.6.1.2 | Euro-American | T2 | RD724 | 0.99 |
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 | 0.98 |
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 |
embR | 1416410 | p.Leu313Arg | missense_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476339 | n.2682G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476356 | n.2699C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476384 | n.2727G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674465 | c.264C>T | synonymous_variant | 0.98 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154512 | p.Gly534Arg | missense_variant | 0.99 |
PPE35 | 2169044 | c.1569G>C | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.23 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878641 | c.-135delG | upstream_gene_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245055 | p.Thr608Asn | missense_variant | 0.98 |
ethR | 4327891 | p.Gly115Arg | missense_variant | 0.99 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338635 | c.-114A>C | upstream_gene_variant | 0.95 |