Run ID: SRR5818648
Sample name:
Date: 04-04-2023 11:40:55
Number of reads: 1462704
Percentage reads mapped: 92.14
Strain: lineage4.2.2.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.2 | Euro-American | H;T;LAM | None | 0.99 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.98 |
lineage4.2.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.97 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8688 | p.Ala463Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576077 | c.730C>T | synonymous_variant | 0.98 |
rpoB | 761489 | c.1683G>A | synonymous_variant | 0.94 |
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 | 1472068 | n.226delG | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474634 | n.977T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.24 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.94 |
katG | 2155542 | c.570G>A | synonymous_variant | 1.0 |
PPE35 | 2169068 | c.1545G>T | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.98 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.97 |