Run ID: ERR2229552
Sample name:
Date: 31-03-2023 17:18:38
Number of reads: 1070594
Percentage reads mapped: 99.44
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 |
---|---|---|---|---|
gyrB | 6549 | p.Gly437Ala | missense_variant | 0.38 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
mshA | 576119 | p.Ala258Thr | missense_variant | 0.29 |
mshA | 576482 | p.Val379Leu | missense_variant | 0.18 |
rpoB | 762472 | p.Ile889Thr | missense_variant | 0.1 |
rpoC | 763987 | c.618C>A | synonymous_variant | 0.18 |
rpoC | 763999 | p.Asp210Glu | missense_variant | 0.17 |
rpoC | 764025 | c.658delG | frameshift_variant | 0.15 |
rpoC | 765665 | p.Asn766Asp | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 779137 | p.Arg50Trp | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_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 |
fabG1 | 1674044 | p.Ala202Gly | missense_variant | 0.19 |
tlyA | 1917777 | c.-163A>G | upstream_gene_variant | 0.12 |
tlyA | 1917911 | c.-29G>A | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2153969 | p.Asp715Tyr | missense_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169717 | p.Asn299Ile | missense_variant | 0.12 |
PPE35 | 2169732 | p.Asn294Ser | missense_variant | 0.14 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.23 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.2 |
PPE35 | 2170139 | c.474G>A | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518946 | p.Val278Leu | missense_variant | 0.11 |
ahpC | 2726089 | c.-104C>A | upstream_gene_variant | 0.11 |
pepQ | 2860284 | c.135G>T | synonymous_variant | 0.12 |
ribD | 2987441 | c.603A>G | synonymous_variant | 0.11 |
fprA | 3474215 | p.Thr70Met | missense_variant | 0.12 |
fprA | 3475328 | p.Arg441Gln | missense_variant | 0.15 |
whiB7 | 3568524 | p.Cys52* | stop_gained | 0.11 |
panD | 4043936 | p.Asp116Tyr | missense_variant | 0.13 |
embC | 4242522 | p.Ala887Glu | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.15 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.17 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.17 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.2 |
embB | 4247395 | c.882C>A | synonymous_variant | 0.11 |
aftB | 4267960 | p.Val293Leu | missense_variant | 0.12 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |