Run ID: ERR502531
Sample name:
Date: 01-04-2023 21:57:20
Number of reads: 14661
Percentage reads mapped: 0.97
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.67 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoC | 763573 | c.204G>C | synonymous_variant | 0.67 |
rpoC | 763621 | c.252C>T | synonymous_variant | 1.0 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.67 |
rpoC | 763633 | c.264T>C | synonymous_variant | 1.0 |
rpoC | 763639 | p.Glu90Asp | missense_variant | 0.67 |
rpoC | 763642 | c.273G>C | synonymous_variant | 1.0 |
rpoC | 763655 | p.Glu96Gln | missense_variant | 0.67 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.67 |
rpoC | 763666 | c.297G>C | synonymous_variant | 1.0 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.67 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
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 | 1.0 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
katG | 2155372 | p.Asp247Gly | missense_variant | 1.0 |
Rv3083 | 3449861 | p.Arg453His | missense_variant | 0.67 |
embA | 4246393 | p.Trp1054* | stop_gained | 1.0 |