Run ID: ERR11068771
Sample name:
Date: 07-04-2023 01:14:49
Number of reads: 3259941
Percentage reads mapped: 99.47
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 | 575371 | c.24C>T | synonymous_variant | 0.12 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.57 |
mshA | 576116 | p.Ala257Pro | missense_variant | 0.3 |
mshA | 576119 | p.Ala258Pro | missense_variant | 0.27 |
ccsA | 619831 | c.-60T>C | upstream_gene_variant | 0.25 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
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 |
fbiC | 1304256 | c.1326G>A | synonymous_variant | 0.12 |
Rv1258c | 1407053 | c.288C>T | synonymous_variant | 0.12 |
Rv1258c | 1407148 | p.Ala65Thr | missense_variant | 0.11 |
Rv1258c | 1407149 | c.192C>T | synonymous_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918066 | p.Ala43Pro | missense_variant | 0.22 |
PPE35 | 2170138 | p.Ser159Pro | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518693 | c.579C>T | synonymous_variant | 0.12 |
eis | 2715569 | c.-237C>T | upstream_gene_variant | 0.29 |
folC | 2746675 | c.924C>A | synonymous_variant | 0.25 |
pepQ | 2860146 | c.273C>T | synonymous_variant | 0.5 |
thyX | 3067971 | c.-26T>C | upstream_gene_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339733 | p.Ala206Thr | missense_variant | 0.4 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3642033 | p.Ala167Thr | missense_variant | 0.17 |
rpoA | 3878559 | c.-53delC | upstream_gene_variant | 0.33 |
clpC1 | 4040256 | p.Ala150Val | missense_variant | 0.12 |
embC | 4242470 | p.Arg870Trp | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4243523 | c.291C>A | synonymous_variant | 0.17 |
embB | 4248605 | c.2092C>T | synonymous_variant | 0.12 |
aftB | 4268333 | c.504C>T | synonymous_variant | 0.11 |
ethR | 4328030 | p.Ala161Gly | missense_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |