Run ID: SRR6896550
Sample name:
Date: 04-04-2023 18:09:35
Number of reads: 676758
Percentage reads mapped: 98.26
Strain: lineage4.3.2.1
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 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 0.98 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761108 | p.Met434Ile | missense_variant | 0.17 | rifampicin |
katG | 2155703 | c.408delC | frameshift_variant | 0.15 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
gyrB | 6581 | p.Thr448Ala | missense_variant | 0.1 |
gyrA | 7222 | c.-80C>T | upstream_gene_variant | 1.0 |
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 | 491443 | p.Ser221Pro | missense_variant | 0.1 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775934 | p.Asp849Glu | missense_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
atpE | 1461077 | c.33C>T | synonymous_variant | 0.14 |
atpE | 1461123 | p.Gly27Arg | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471834 | n.-12G>T | upstream_gene_variant | 0.12 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473980 | n.325dupG | non_coding_transcript_exon_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155096 | p.Tyr339Cys | missense_variant | 0.11 |
PPE35 | 2168354 | c.2259G>T | synonymous_variant | 0.11 |
PPE35 | 2168457 | p.Val719Ala | missense_variant | 0.15 |
PPE35 | 2169310 | p.Gly435Arg | missense_variant | 0.11 |
PPE35 | 2169691 | c.921delC | frameshift_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714552 | p.Ser261Pro | missense_variant | 0.1 |
pepQ | 2859372 | c.1047G>A | synonymous_variant | 0.13 |
pepQ | 2859750 | c.669C>A | synonymous_variant | 0.11 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086901 | p.Arg28Cys | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568650 | c.30C>A | synonymous_variant | 0.88 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4038963 | p.Asp581Val | missense_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |