Run ID: ERR4812639
Sample name:
Date: 01-04-2023 12:12:48
Number of reads: 694417
Percentage reads mapped: 99.48
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 | 0.96 |
lineage4.1.2 | Euro-American | T;H | None | 0.92 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 0.92 |
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 | 8040 | p.Gly247Ser | missense_variant | 0.25 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.9 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.87 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.31 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.86 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775677 | p.Lys935Arg | missense_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304364 | c.1435delC | frameshift_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155149 | p.Trp321Phe | missense_variant | 0.91 |
katG | 2155664 | p.Pro150Thr | missense_variant | 0.29 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 0.84 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 0.2 |
ald | 3086650 | c.-170C>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 |
Rv3236c | 3612100 | c.1017C>A | synonymous_variant | 0.11 |
embC | 4240541 | p.Thr227Ala | missense_variant | 0.73 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.93 |
embA | 4245116 | c.1884C>A | synonymous_variant | 0.12 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.38 |
embB | 4248630 | p.Pro706Gln | missense_variant | 0.2 |
embB | 4248691 | c.2178C>A | synonymous_variant | 0.13 |
ethA | 4326350 | p.Ser375Phe | missense_variant | 0.15 |
ethA | 4327175 | p.Phe100Ser | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407768 | p.Leu145Phe | missense_variant | 0.14 |