Run ID: ERR2513005
Sample name:
Date: 31-03-2023 19:23:45
Number of reads: 2339960
Percentage reads mapped: 98.08
Strain: lineage4.6
Drug-resistance: Other
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 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.73 | 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 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.37 |
mshA | 575434 | c.87C>T | synonymous_variant | 1.0 |
rpoC | 763644 | p.Met92Thr | missense_variant | 0.97 |
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 | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168080 | p.Thr845Ala | missense_variant | 1.0 |
PPE35 | 2170198 | p.Ala139Thr | missense_variant | 0.97 |
PPE35 | 2170792 | c.-180T>C | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pepQ | 2860360 | p.Asp20Gly | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612698 | p.Leu140Arg | missense_variant | 0.97 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.35 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.98 |
embA | 4244970 | c.1738C>T | synonymous_variant | 1.0 |
aftB | 4267118 | c.1719G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |