Run ID: ERR11043389
Sample name:
Date: 31-03-2023 11:33:28
Number of reads: 3253552
Percentage reads mapped: 99.72
Strain: lineage4.7
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 |
lineage4.7 | Euro-American (mainly T) | T1;T5 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761140 | p.His445Arg | missense_variant | 1.0 | rifampicin |
inhA | 1674262 | p.Ile21Val | missense_variant | 1.0 | isoniazid |
katG | 2156110 | p.Val1Ala | missense_variant | 1.0 | isoniazid |
pncA | 2289175 | c.66dupC | frameshift_variant | 1.0 | pyrazinamide, pyrazinamide |
ahpC | 2726141 | c.-52C>T | upstream_gene_variant | 1.0 | isoniazid |
embB | 4247729 | p.Gly406Cys | missense_variant | 1.0 | ethambutol |
ethA | 4327132 | c.341delA | frameshift_variant | 1.0 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7270 | c.-32C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 761265 | p.Asn487His | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474294 | n.637C>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1834202 | p.Asn221Asp | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102444 | c.596_598dupGCG | conservative_inframe_insertion | 1.0 |
PPE35 | 2170675 | c.-63G>C | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746280 | p.Ile440Ser | missense_variant | 1.0 |
thyA | 3073873 | p.Ile200Ser | missense_variant | 1.0 |
thyA | 3074356 | p.Ser39Gln | missense_variant | 1.0 |
whiB7 | 3568428 | c.252A>C | synonymous_variant | 0.26 |
whiB7 | 3568431 | c.249C>G | synonymous_variant | 0.19 |
rpoA | 3877860 | c.648C>A | synonymous_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.21 |
clpC1 | 4040235 | p.Gly157Ala | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4249732 | c.3219C>G | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |