Run ID: ERR2652956
Sample name:
Date: 31-03-2023 22:25:10
Number of reads: 822012
Percentage reads mapped: 99.76
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 | 7265 | c.2026T>A | stop_lost&splice_region_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8933 | c.1632G>A | synonymous_variant | 0.13 |
mshA | 576287 | p.Arg314Trp | missense_variant | 0.11 |
ccsA | 620028 | c.138G>A | synonymous_variant | 0.15 |
rpoB | 761453 | c.1647C>T | synonymous_variant | 0.12 |
mmpL5 | 777895 | p.Gln196* | stop_gained | 0.13 |
fbiC | 1303643 | p.Pro238Leu | missense_variant | 1.0 |
fbiC | 1304582 | p.Asn551Ile | missense_variant | 0.15 |
Rv1258c | 1407381 | c.-41G>T | upstream_gene_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476405 | n.2748C>A | non_coding_transcript_exon_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168281 | p.Pro778Ser | missense_variant | 0.11 |
PPE35 | 2169133 | p.Ala494Thr | missense_variant | 0.13 |
PPE35 | 2170793 | c.-181A>T | upstream_gene_variant | 0.11 |
folC | 2747453 | c.145delC | frameshift_variant | 0.14 |
pepQ | 2860164 | c.255C>A | synonymous_variant | 0.13 |
thyA | 3074329 | p.Lys48Met | missense_variant | 0.12 |
ald | 3086804 | c.-16A>G | upstream_gene_variant | 0.1 |
fbiD | 3339716 | p.Gln200Arg | missense_variant | 0.11 |
Rv3083 | 3449832 | c.1329T>C | synonymous_variant | 0.11 |
fprA | 3474008 | c.4_5dupCG | frameshift_variant | 0.18 |
fprA | 3474080 | p.Ala25Val | missense_variant | 0.12 |
fprA | 3474573 | c.567C>T | synonymous_variant | 0.13 |
panD | 4044309 | c.-28C>T | upstream_gene_variant | 0.12 |
embC | 4240860 | p.Leu333Arg | missense_variant | 1.0 |
embC | 4241264 | p.Gly468Ser | missense_variant | 0.11 |
aftB | 4267922 | c.915G>A | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |