Run ID: SRR4033489
Sample name:
Date: 04-04-2023 06:07:46
Number of reads: 999864
Percentage reads mapped: 99.68
Strain: lineage4.3.2.1
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 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.2 | Euro-American (LAM) | LAM3 | None | 0.99 |
lineage4.3.2.1 | Euro-American (LAM) | LAM3 | RD761 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155660 | c.451delG | frameshift_variant | 0.11 | isoniazid |
pncA | 2288730 | p.Ala171Val | missense_variant | 0.12 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5520 | p.Pro94Leu | missense_variant | 1.0 |
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 | 8508 | p.Glu403Lys | missense_variant | 0.12 |
gyrA | 9059 | c.1758G>A | synonymous_variant | 0.1 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
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 | 1302887 | c.-43delG | upstream_gene_variant | 0.13 |
fbiC | 1304381 | p.Ala484Val | missense_variant | 0.14 |
fbiC | 1305076 | p.Pro716Thr | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472337 | n.492C>T | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674082 | c.-120G>A | upstream_gene_variant | 0.1 |
inhA | 1674952 | p.Pro251Ala | missense_variant | 0.18 |
rpsA | 1834675 | c.1138_1142delATGGC | frameshift_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168473 | c.2139delC | frameshift_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289019 | p.Gly75Ser | missense_variant | 0.14 |
Rv2752c | 3064656 | c.1536G>A | synonymous_variant | 0.1 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.22 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039330 | p.Ala459Thr | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245943 | p.Arg904His | missense_variant | 0.11 |
embA | 4246221 | p.Leu997Phe | missense_variant | 0.11 |
aftB | 4267851 | p.Gln329Leu | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |