Run ID: ERR4817301
Sample name:
Date: 01-04-2023 14:54:56
Number of reads: 91472
Percentage reads mapped: 61.57
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 | 0.89 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.67 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.67 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.67 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.5 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.4 |
rpoC | 763627 | p.Lys86Asn | missense_variant | 0.4 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 1.0 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 1.0 |
rpoC | 764641 | c.1272C>T | synonymous_variant | 1.0 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 1.0 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 1.0 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
rpoC | 764781 | p.Ser471Thr | missense_variant | 0.67 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472107 | n.262A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472279 | n.434T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472368 | n.523A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472767 | n.922G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472955 | n.1110delC | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472958 | n.1113_1114insC | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473022 | n.1177G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473317 | n.1472G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474275 | n.618T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474662 | n.1005C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.67 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.67 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4248639 | p.Ile709Thr | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |