Run ID: ERR4024811
Sample name:
Date: 01-04-2023 04:09:33
Number of reads: 1673503
Percentage reads mapped: 99.62
Strain: lineage4.3;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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 0.3 |
lineage4.1 | Euro-American | T;X;H | None | 0.68 |
lineage4.1.2 | Euro-American | T;H | None | 0.65 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.66 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.98 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.98 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.81 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.65 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.64 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.35 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.76 |
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 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168703 | p.Gly637Val | missense_variant | 0.31 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.72 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.4 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339040 | c.-78T>C | upstream_gene_variant | 0.67 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640393 | c.-150A>C | upstream_gene_variant | 0.69 |
rpoA | 3878601 | c.-95delG | upstream_gene_variant | 0.38 |
rpoA | 3878613 | c.-113_-107delCAACCCA | upstream_gene_variant | 0.37 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.32 |
clpC1 | 4038405 | p.Val767Ala | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.66 |
embB | 4248043 | c.1530C>G | synonymous_variant | 0.66 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.24 |
gid | 4408312 | c.-110C>T | upstream_gene_variant | 0.69 |