Run ID: SRR8692828
Sample name:
Date: 13-08-2023 21:05:35
Number of reads: NA
Percentage reads mapped: NA
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 |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.99 | linezolid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.1 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.11 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.11 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472549 | n.704G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472605 | n.760G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473971 | n.314G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475299 | n.1642G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475863 | n.2206G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476668 | n.3011C>A | non_coding_transcript_exon_variant | 0.22 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.15 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.19 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.16 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.17 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.16 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.14 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.13 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.11 |