Run ID: ERR4814903
Sample name:
Date: 01-04-2023 13:33:32
Number of reads: 2123637
Percentage reads mapped: 96.85
Strain: lineage4.3.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 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 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | 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 | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4268790 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408203 | c.-1A>G | upstream_gene_variant | 1.0 |
whiB6 | 4338200 | c.-2061_321del | start_lost&conservative_inframe_deletion | 1.0 |