Run ID: SRR7131018
Sample name:
Date: 04-04-2023 18:41:45
Number of reads: 1043698
Percentage reads mapped: 100.0
Strain: lineage4.3.1
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 |
lineage4.3.1 | Euro-American (LAM) | LAM9 | 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 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.29 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.23 |
ccsA | 620257 | p.Ile123Val | missense_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775793 | c.2688C>T | synonymous_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407442 | c.-102T>C | upstream_gene_variant | 0.11 |
embR | 1416190 | c.1158C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472458 | n.613A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472605 | n.760G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472827 | n.982G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473704 | n.47C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473706 | n.49A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473930 | n.273A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473954 | n.297A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474875 | n.1218G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474876 | n.1219T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475637 | n.1980T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476504 | n.2847T>C | non_coding_transcript_exon_variant | 0.11 |
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 |
Rv3083 | 3449369 | p.Asn289Ser | missense_variant | 0.11 |
Rv3083 | 3449375 | p.Leu291Pro | missense_variant | 0.1 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4240389 | p.Asn176Ser | missense_variant | 0.11 |
embC | 4241959 | c.2097A>G | synonymous_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |