Run ID: ERR2228901
Sample name:
Date: 31-03-2023 16:25:20
Number of reads: 1349495
Percentage reads mapped: 99.61
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 |
fgd1 | 491357 | p.Phe192Tyr | missense_variant | 0.15 |
fgd1 | 491456 | p.Ile225Ser | missense_variant | 0.12 |
mshA | 575596 | c.249C>A | synonymous_variant | 0.12 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.17 |
ccsA | 620122 | c.236delG | frameshift_variant | 0.22 |
mmpL5 | 775588 | c.2893T>A | stop_lost&splice_region_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775686 | p.Leu932His | missense_variant | 0.12 |
mmpL5 | 775693 | p.Ala930Ser | missense_variant | 0.12 |
mmpL5 | 775813 | p.Phe890Val | missense_variant | 0.11 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304425 | p.Leu499Met | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472801 | n.956G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.11 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.1 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.15 |
PPE35 | 2170392 | p.Gly74Ala | missense_variant | 0.15 |
PPE35 | 2170415 | c.198A>G | synonymous_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518762 | p.Met216Ile | missense_variant | 0.12 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.17 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.15 |
eis | 2715018 | c.315C>T | synonymous_variant | 0.11 |
folC | 2746221 | p.Ala460Ser | missense_variant | 0.14 |
folC | 2746440 | p.Val387Met | missense_variant | 0.15 |
folC | 2746462 | c.1137C>T | synonymous_variant | 0.13 |
thyX | 3067616 | c.330C>T | synonymous_variant | 0.18 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fprA | 3474979 | p.Arg325Cys | missense_variant | 0.12 |
fprA | 3474996 | c.990C>A | synonymous_variant | 0.13 |
Rv3236c | 3612123 | p.Ala332Ser | missense_variant | 0.17 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.17 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.19 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244184 | p.Ser318Leu | missense_variant | 0.12 |
embA | 4244780 | c.1548C>G | synonymous_variant | 0.12 |
embA | 4245943 | p.Arg904Leu | missense_variant | 0.15 |
aftB | 4268776 | c.60delG | frameshift_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |