Run ID: ERR2516132
Sample name:
Date: 31-03-2023 21:19:48
Number of reads: 748368
Percentage reads mapped: 99.23
Strain: lineage4.1.2.1
Drug-resistance: HR-TB
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 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.93 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 575857 | c.510G>A | synonymous_variant | 0.12 |
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 |
mmpR5 | 779185 | p.Gly66Trp | missense_variant | 0.16 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1407489 | c.-149G>A | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.33 |
rpsA | 1834438 | c.897C>T | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918106 | p.Thr56Ile | missense_variant | 0.13 |
katG | 2154900 | c.1212G>A | synonymous_variant | 0.12 |
katG | 2155552 | p.Arg187Leu | missense_variant | 0.14 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.11 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.14 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
Rv2752c | 3066299 | c.-108C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449396 | p.Cys298Phe | missense_variant | 0.12 |
fprA | 3473998 | c.-9G>A | upstream_gene_variant | 1.0 |
fprA | 3473998 | c.-10_-9insA | upstream_gene_variant | 1.0 |
fprA | 3474594 | c.588C>T | synonymous_variant | 0.12 |
fprA | 3474856 | p.Val284Leu | missense_variant | 0.13 |
fprA | 3475205 | p.Glu400Val | missense_variant | 0.25 |
fbiA | 3641309 | p.Ala256Gly | missense_variant | 0.12 |
fbiB | 3642148 | p.Val205Ala | missense_variant | 0.15 |
fbiB | 3642692 | c.1158C>A | synonymous_variant | 0.12 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.92 |
embA | 4244930 | c.1698G>A | synonymous_variant | 0.22 |
embA | 4245305 | c.2075_2076dupTG | frameshift_variant | 0.13 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.36 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.15 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.13 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.13 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.13 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.13 |
ubiA | 4268929 | p.Gly302Val | missense_variant | 0.12 |
whiB6 | 4338189 | c.333G>A | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |