Run ID: ERR3468653
Sample name:
Date: 01-04-2023 02:20:16
Number of reads: 47471
Percentage reads mapped: 5.7
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476483 | n.2826G>A | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |