Run ID: ERR4816746
Sample name:
Date: 01-04-2023 14:36:29
Number of reads: 2964317
Percentage reads mapped: 98.08
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576263 | c.916C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474529 | n.872A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474581 | n.924C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474826 | n.1169T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474852 | n.1195T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3064875 | c.1317C>G | synonymous_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 1.0 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3474119 | p.Met38Thr | missense_variant | 1.0 |
fprA | 3474925 | p.Thr307Ala | missense_variant | 1.0 |
fbiA | 3641477 | p.Asp312Gly | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338596 | c.-75G>A | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |