Run ID: ERR1950028
Sample name:
Date: 31-03-2023 15:37:52
Number of reads: 163561
Percentage reads mapped: 99.65
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 |
fgd1 | 490738 | c.-45C>T | upstream_gene_variant | 0.33 |
mshA | 575381 | p.Leu12Val | missense_variant | 0.33 |
rpoB | 761371 | p.Ile522Asn | missense_variant | 0.33 |
rpoC | 763897 | p.Lys176Asn | missense_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302948 | c.18T>G | synonymous_variant | 0.5 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304629 | p.Phe567Ile | missense_variant | 0.5 |
Rv1258c | 1406809 | p.Ala178Thr | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471684 | n.-162A>T | upstream_gene_variant | 0.4 |
rrs | 1472504 | n.659A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473995 | n.338G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289452 | c.-211C>G | upstream_gene_variant | 0.25 |
pncA | 2289561 | c.-320T>G | upstream_gene_variant | 0.5 |
kasA | 2518628 | p.Ser172Ala | missense_variant | 0.5 |
Rv2752c | 3065572 | p.Glu207Gly | missense_variant | 0.5 |
thyA | 3074548 | c.-77T>G | upstream_gene_variant | 0.4 |
alr | 3840230 | c.1191T>A | synonymous_variant | 0.5 |
ddn | 3987025 | p.Val61Gly | missense_variant | 0.67 |
ddn | 3987103 | p.Met87Thr | missense_variant | 0.18 |
clpC1 | 4038314 | c.2391T>G | synonymous_variant | 0.4 |
clpC1 | 4038876 | p.Leu610Pro | missense_variant | 0.22 |
embC | 4240204 | c.342T>A | synonymous_variant | 0.67 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244184 | p.Ser318Leu | missense_variant | 0.5 |
aftB | 4267161 | p.Val559Asp | missense_variant | 0.33 |
aftB | 4267179 | c.1657delT | frameshift_variant | 0.29 |
ubiA | 4269820 | p.Val5Ala | missense_variant | 0.29 |
ubiA | 4269957 | c.-124A>T | upstream_gene_variant | 0.29 |
ethR | 4327000 | c.-549G>A | upstream_gene_variant | 0.22 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |