Run ID: ERR1274699
Sample name:
Date: 31-03-2023 13:29:15
Number of reads: 20519
Percentage reads mapped: 98.61
Strain: lineage4.9
Drug-resistance: Sensitive
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765719 | p.Glu784Gln | missense_variant | 1.0 |
fbiC | 1304085 | c.1155C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471819 | n.-27C>G | upstream_gene_variant | 0.33 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472792 | n.947G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473112 | n.1267A>C | non_coding_transcript_exon_variant | 0.14 |
PPE35 | 2168765 | p.Ser616Arg | missense_variant | 0.12 |
PPE35 | 2169122 | c.1491C>G | synonymous_variant | 0.25 |
PPE35 | 2169317 | c.1296C>T | synonymous_variant | 0.29 |
PPE35 | 2169671 | c.942C>G | synonymous_variant | 0.25 |
PPE35 | 2169674 | c.939T>C | synonymous_variant | 0.25 |
PPE35 | 2169680 | c.933A>G | synonymous_variant | 0.25 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.4 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714747 | p.Leu196Ile | missense_variant | 1.0 |
ahpC | 2726670 | p.Glu160* | stop_gained | 0.67 |
clpC1 | 4039821 | p.Ala295Val | missense_variant | 0.5 |
aftB | 4267325 | c.1512G>T | synonymous_variant | 1.0 |