Run ID: SRR13837658
Sample name:
Date: 03-04-2023 09:15:19
Number of reads: 293870
Percentage reads mapped: 95.02
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 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5807 | p.Val190Phe | missense_variant | 1.0 |
gyrA | 6898 | c.-404G>C | upstream_gene_variant | 1.0 |
gyrA | 8039 | c.738T>C | synonymous_variant | 1.0 |
mshA | 575293 | c.-55T>A | upstream_gene_variant | 1.0 |
mshA | 575414 | p.Gly23Ser | missense_variant | 1.0 |
rpoC | 765124 | c.1755G>C | synonymous_variant | 1.0 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.15 |
rpsA | 1834248 | p.His236Leu | missense_variant | 1.0 |
katG | 2154449 | p.Ala555Ser | missense_variant | 1.0 |
PPE35 | 2170218 | p.Ala132Glu | missense_variant | 1.0 |
eis | 2715396 | c.-65delT | upstream_gene_variant | 1.0 |
ribD | 2987136 | p.Val100Ile | missense_variant | 1.0 |
ribD | 2987590 | p.Leu251Arg | missense_variant | 1.0 |
Rv2752c | 3064996 | p.Thr399Asn | missense_variant | 1.0 |
alr | 3841281 | p.His47Arg | missense_variant | 1.0 |
clpC1 | 4039292 | c.1413C>A | synonymous_variant | 0.88 |
clpC1 | 4039426 | p.Lys427Gln | missense_variant | 1.0 |
embA | 4243228 | c.-5G>T | upstream_gene_variant | 1.0 |
embA | 4243540 | p.Ala103Asp | missense_variant | 1.0 |
embA | 4244146 | p.Asp305Ala | missense_variant | 1.0 |
embB | 4249506 | c.2994delG | frameshift_variant | 1.0 |