Run ID: ERR2653070
Sample name:
Date: 31-03-2023 22:29:02
Number of reads: 1071145
Percentage reads mapped: 99.44
Strain: lineage4.3.3
Drug-resistance: MDR-TB
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 | 0.99 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.96 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289095 | p.Asp49Glu | missense_variant | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326721 | c.752dupG | frameshift_variant | 0.15 | ethionamide, ethionamide |
ethA | 4326800 | c.672_673dupGC | frameshift_variant | 0.33 | ethionamide, ethionamide |
ethA | 4326885 | c.587_588dupAC | frameshift_variant | 0.15 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5723 | p.Ala162Ser | missense_variant | 1.0 |
gyrB | 6009 | p.Leu257Pro | missense_variant | 0.11 |
gyrB | 6765 | p.Leu509Pro | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7584 | p.Ser95Ala | missense_variant | 0.88 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 0.95 |
gyrA | 8164 | p.Ala288Asp | missense_variant | 0.18 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575240 | c.-108G>A | upstream_gene_variant | 1.0 |
mshA | 575356 | c.9T>C | synonymous_variant | 0.11 |
rpoB | 761890 | p.Val695Glu | missense_variant | 0.11 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302822 | c.-109T>C | upstream_gene_variant | 0.1 |
Rv1258c | 1406404 | p.Val313Ile | missense_variant | 0.33 |
atpE | 1461156 | p.Gly38Arg | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474944 | n.1287G>C | non_coding_transcript_exon_variant | 0.12 |
inhA | 1674954 | c.753G>C | synonymous_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102885 | p.Pro53Leu | missense_variant | 0.18 |
katG | 2156244 | c.-135_-134delCG | upstream_gene_variant | 0.14 |
PPE35 | 2170404 | p.Ala70Gly | missense_variant | 0.11 |
PPE35 | 2170422 | p.Ala64Gly | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
eis | 2715168 | c.165T>C | synonymous_variant | 0.17 |
folC | 2746835 | p.Ser255Leu | missense_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087009 | p.Val64Leu | missense_variant | 0.12 |
ald | 3087619 | c.801_802dupAG | frameshift_variant | 0.79 |
Rv3083 | 3449357 | p.Asn285Ile | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640922 | p.Gln127Arg | missense_variant | 0.17 |
rpoA | 3878630 | c.-123G>C | upstream_gene_variant | 0.17 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4040752 | c.-48C>G | upstream_gene_variant | 0.11 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243159 | c.-74C>T | upstream_gene_variant | 0.11 |
embA | 4243814 | c.585delT | frameshift_variant | 0.12 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.14 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.14 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.12 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.12 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.11 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |
gid | 4408313 | c.-111A>G | upstream_gene_variant | 0.12 |