Run ID: ERR4818869
Sample name:
Date: 01-04-2023 15:48:22
Number of reads: 7041146
Percentage reads mapped: 99.5
Strain: lineage4.2.2.2
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.99 |
lineage4.2.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.46 | 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 | 8688 | p.Ala463Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
rpoC | 767228 | p.Ser1287Gln | 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 | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472803 | n.958T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472892 | n.1047T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3065353 | p.Arg280Gln | missense_variant | 1.0 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | 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 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |