Run ID: ERR025887
Sample name:
Date: 31-03-2023 08:19:02
Number of reads: 287228
Percentage reads mapped: 32.0
Strain: lineage1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 0.06 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.43 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 0.5 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.75 |
fgd1 | 490756 | c.-27T>G | upstream_gene_variant | 0.67 |
mshA | 575368 | c.21T>C | synonymous_variant | 0.67 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.8 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.8 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.5 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.33 |
fbiC | 1302821 | c.-110G>A | upstream_gene_variant | 0.29 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 0.57 |
embR | 1416898 | c.450C>T | synonymous_variant | 0.67 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.4 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.67 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 0.5 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.38 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 0.67 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.62 |
Rv3236c | 3612009 | p.Ala370Thr | missense_variant | 1.0 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiB | 3642772 | p.Asp413Ala | missense_variant | 0.5 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.67 |
embC | 4239763 | c.-100C>T | upstream_gene_variant | 0.5 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.29 |
embA | 4244420 | c.1188G>C | synonymous_variant | 0.5 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.67 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.5 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.4 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |