Run ID: SRR22528570
Sample name:
Date: 04-04-2023 04:18:58
Number of reads: 769165
Percentage reads mapped: 99.63
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 | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 1.0 | rifampicin |
katG | 2155109 | p.Ile335Val | missense_variant | 0.17 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7516 | p.Lys72Met | missense_variant | 0.13 |
gyrA | 7555 | p.His85Arg | missense_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576123 | p.Leu259Arg | missense_variant | 0.12 |
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 |
rpsL | 781467 | c.-93G>C | upstream_gene_variant | 0.11 |
fbiC | 1303701 | c.771C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472119 | n.274G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475352 | n.1695T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.14 |
rpsA | 1833490 | c.-52C>G | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103167 | c.-125A>T | upstream_gene_variant | 0.13 |
ndh | 2103199 | c.-157G>T | upstream_gene_variant | 0.15 |
katG | 2156410 | c.-299T>C | upstream_gene_variant | 0.12 |
PPE35 | 2168287 | p.Ile776Val | missense_variant | 0.12 |
PPE35 | 2170705 | c.-93T>C | upstream_gene_variant | 0.11 |
Rv1979c | 2222214 | c.951C>T | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
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 |
fprA | 3474342 | p.Leu112Phe | missense_variant | 0.15 |
Rv3236c | 3612853 | c.264C>T | synonymous_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embC | 4242182 | p.Ala774Ser | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246558 | c.45G>T | synonymous_variant | 0.2 |
embB | 4246582 | c.69T>G | synonymous_variant | 0.13 |
whiB6 | 4338252 | p.Phe90Leu | missense_variant | 0.53 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |