Run ID: SRR5341258
Sample name:
Date: 04-04-2023 10:12:46
Number of reads: 1216814
Percentage reads mapped: 99.78
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.95 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.88 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1473246 | n.1401A>G | non_coding_transcript_exon_variant | 0.92 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.15 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.11 |
mshA | 576117 | p.Ala257Asp | missense_variant | 0.12 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.3 |
rpoB | 761152 | p.Leu449Gln | missense_variant | 0.11 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.12 |
Rv1258c | 1406943 | c.397_398insGC | frameshift_variant | 0.14 |
Rv1258c | 1406946 | p.Ala132Gly | missense_variant | 0.14 |
Rv1258c | 1406948 | c.391_392delGC | frameshift_variant | 0.14 |
fabG1 | 1673357 | c.-83G>A | upstream_gene_variant | 0.15 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.16 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.16 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.21 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.2 |
katG | 2155191 | c.921A>C | synonymous_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.34 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.34 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 0.11 |
thyX | 3067340 | c.606G>A | synonymous_variant | 0.13 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.15 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.1 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.16 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.29 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.29 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.29 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.15 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.14 |
aftB | 4268810 | c.27G>A | synonymous_variant | 0.13 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.11 |