Run ID: ERR11068819
Sample name:
Date: 07-04-2023 03:02:15
Number of reads: 2955594
Percentage reads mapped: 99.51
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 |
gyrA | 9647 | c.2346C>G | synonymous_variant | 0.22 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.33 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 766064 | p.Val899Ile | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303965 | c.1035G>A | synonymous_variant | 0.2 |
fbiC | 1304014 | p.Pro362Ser | missense_variant | 0.2 |
fbiC | 1304193 | c.1263G>A | synonymous_variant | 0.17 |
Rv1258c | 1406984 | c.357A>C | synonymous_variant | 0.29 |
Rv1258c | 1407012 | p.Ala110Val | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rpsA | 1834841 | p.Lys434Glu | missense_variant | 0.12 |
tlyA | 1917970 | c.31_33delCTAinsTTG | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
eis | 2715085 | p.Ser83Asn | missense_variant | 0.17 |
pepQ | 2859997 | p.Ala141Val | missense_variant | 0.11 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641876 | c.342C>T | synonymous_variant | 0.11 |
clpC1 | 4038218 | c.2487G>A | synonymous_variant | 0.18 |
embC | 4240432 | c.570C>T | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4244324 | c.1092T>C | synonymous_variant | 0.11 |
embB | 4246619 | p.Ile36Val | missense_variant | 0.18 |
embB | 4248329 | p.Met606Leu | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408468 | c.-266G>T | upstream_gene_variant | 0.12 |