Run ID: ERR11050207
Sample name:
Date: 02-04-2023 16:02:32
Number of reads: 3554526
Percentage reads mapped: 99.81
Strain: lineage4.3.4.2
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 | 1.0 |
lineage4.3.4 | Euro-American (LAM) | LAM | RD174 | 1.0 |
lineage4.3.4.2 | Euro-American (LAM) | LAM1;LAM4;LAM11 | RD174 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761109 | p.Asp435Tyr | missense_variant | 0.98 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.99 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embA | 4243222 | c.-11C>A | upstream_gene_variant | 1.0 | ethambutol |
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 |
fgd1 | 491683 | p.Val301Leu | missense_variant | 1.0 |
mshA | 576106 | c.759C>G | synonymous_variant | 0.33 |
mshA | 576113 | p.Arg256Gly | missense_variant | 0.3 |
mshA | 576442 | p.Cys365Trp | missense_variant | 0.36 |
mshA | 576453 | p.Val369Gly | missense_variant | 0.27 |
mshA | 576456 | p.Val370Gly | missense_variant | 0.36 |
mshA | 576468 | p.Val374Gly | missense_variant | 0.27 |
mshA | 576489 | p.Val381Gly | missense_variant | 0.33 |
mshA | 576606 | p.Ala420Gly | missense_variant | 0.36 |
mshA | 576613 | c.1266A>C | synonymous_variant | 0.5 |
mshA | 576616 | c.1269G>C | synonymous_variant | 0.4 |
mshA | 576618 | p.His424Pro | missense_variant | 0.33 |
rpoC | 764367 | p.Gly333Ala | missense_variant | 0.23 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777883 | p.Gly200Arg | missense_variant | 0.34 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303157 | p.His76Pro | missense_variant | 0.24 |
embR | 1416430 | c.918G>C | synonymous_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1475795 | n.2138A>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476058 | n.2401T>G | non_coding_transcript_exon_variant | 0.21 |
fabG1 | 1673553 | p.Asp38Glu | missense_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170386 | p.Leu76Arg | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519071 | p.Asp319Glu | missense_variant | 0.53 |
Rv2752c | 3064823 | p.Val457Leu | missense_variant | 0.18 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339734 | p.Ala206Gly | missense_variant | 1.0 |
fbiD | 3339751 | p.Ala212Pro | missense_variant | 0.44 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474213 | p.Lys69Asn | missense_variant | 0.19 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
Rv3236c | 3612268 | c.849C>T | synonymous_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.85 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4240409 | p.Pro183Ala | missense_variant | 0.32 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243682 | c.450T>G | synonymous_variant | 0.2 |
embB | 4246527 | p.Ala5Gly | missense_variant | 0.52 |
embB | 4247016 | p.Ser168Trp | missense_variant | 0.27 |
embB | 4247020 | c.507C>G | synonymous_variant | 0.38 |
embB | 4248328 | c.1815G>C | synonymous_variant | 0.19 |
aftB | 4267981 | p.Arg286Gly | missense_variant | 0.33 |
whiB6 | 4338200 | p.Asp108His | missense_variant | 0.36 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |