Run ID: ERR9786705
Sample name:
Date: 02-04-2023 12:40:38
Number of reads: 822004
Percentage reads mapped: 74.27
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 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 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.1 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781510 | c.-50G>A | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472581 | n.736A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476025 | n.2368G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476043 | n.2387_2388delTG | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476048 | n.2391G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476050 | n.2394_2395insTG | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476420 | n.2763G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476433 | n.2776C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476528 | n.2871A>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.13 |
rpsA | 1834405 | c.864C>T | synonymous_variant | 0.13 |
rpsA | 1834408 | c.867C>T | synonymous_variant | 0.13 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.14 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.14 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.12 |
rpsA | 1834438 | c.897C>T | synonymous_variant | 0.12 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.15 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.17 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.2 |
rpsA | 1834480 | c.939C>G | synonymous_variant | 0.2 |
rpsA | 1834519 | c.978G>C | synonymous_variant | 0.11 |
rpsA | 1834528 | c.987T>G | synonymous_variant | 0.11 |
rpsA | 1834531 | c.990C>T | synonymous_variant | 0.11 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.1 |
rpsA | 1834552 | c.1011G>C | synonymous_variant | 0.1 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.1 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.1 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | 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 |
clpC1 | 4039246 | p.Val487Leu | missense_variant | 0.95 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |