Run ID: SRR1002679
Sample name:
Date: 02-04-2023 14:19:29
Number of reads: 2058469
Percentage reads mapped: 99.32
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 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 | 9796 | p.Gly832Ala | missense_variant | 1.0 |
fgd1 | 490677 | c.-105_-104delCA | upstream_gene_variant | 0.11 |
fgd1 | 490690 | c.-93C>A | upstream_gene_variant | 0.12 |
fgd1 | 491122 | p.Ile114Val | missense_variant | 0.12 |
mshA | 575306 | c.-42T>C | upstream_gene_variant | 0.13 |
mshA | 575308 | c.-40A>G | upstream_gene_variant | 0.12 |
mshA | 575372 | p.Gly9Ser | missense_variant | 0.13 |
mshA | 575831 | p.Gly162Cys | missense_variant | 0.12 |
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 | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475075 | n.1418A>C | non_coding_transcript_exon_variant | 0.35 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2169110 | c.1503T>C | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289584 | c.-343A>G | upstream_gene_variant | 0.12 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.11 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.1 |
kasA | 2519041 | c.927C>T | synonymous_variant | 0.15 |
Rv3236c | 3613242 | c.-126G>T | upstream_gene_variant | 0.13 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.11 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 1.0 |
panD | 4044237 | c.45G>A | synonymous_variant | 0.25 |
embC | 4241372 | p.Arg504Gly | missense_variant | 0.1 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243127 | p.Ala1089Thr | missense_variant | 0.12 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.1 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.12 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.12 |
embB | 4247170 | c.657G>T | synonymous_variant | 0.15 |
aftB | 4268226 | p.Ala204Val | missense_variant | 0.11 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |