Run ID: ERR4819969
Sample name:
Date: 01-04-2023 16:24:29
Number of reads: 544132
Percentage reads mapped: 98.36
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8656 | p.Ile452Thr | missense_variant | 1.0 |
gyrA | 9071 | c.1770G>A | synonymous_variant | 0.22 |
fgd1 | 490965 | c.183C>T | synonymous_variant | 0.18 |
fgd1 | 491247 | c.465C>T | synonymous_variant | 1.0 |
rpoC | 766737 | p.Arg1123Gln | missense_variant | 0.2 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776664 | p.Thr606Asn | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673961 | c.-241A>C | upstream_gene_variant | 1.0 |
inhA | 1674951 | c.752delC | frameshift_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170812 | c.-200G>A | upstream_gene_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.75 |
kasA | 2519286 | p.Tyr391Cys | missense_variant | 0.15 |
pepQ | 2859318 | p.Lys367Asn | missense_variant | 1.0 |
Rv2752c | 3065102 | p.Thr364Ala | missense_variant | 0.15 |
thyX | 3067747 | p.Val67Leu | missense_variant | 0.11 |
ald | 3087733 | p.Val305Ala | missense_variant | 0.18 |
Rv3083 | 3449810 | c.1308dupC | frameshift_variant | 0.13 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.2 |
rpoA | 3878284 | p.Glu75Ala | missense_variant | 0.2 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.22 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.2 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.2 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.2 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.2 |
clpC1 | 4040823 | c.-119C>T | upstream_gene_variant | 0.1 |
embC | 4240602 | p.Ala247Val | missense_variant | 0.12 |
embC | 4240828 | c.967_969delCCT | conservative_inframe_deletion | 0.18 |
embC | 4241271 | p.Leu470Pro | missense_variant | 0.14 |
embC | 4241761 | c.1899G>A | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243310 | c.78G>T | synonymous_variant | 1.0 |
embA | 4245863 | p.Ile877Met | missense_variant | 0.14 |
embB | 4247903 | c.1390C>A | synonymous_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407715 | c.485_487dupTCA | conservative_inframe_insertion | 0.11 |