Run ID: ERR2228905
Sample name:
Date: 31-03-2023 16:25:29
Number of reads: 940533
Percentage reads mapped: 99.55
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 |
ccsA | 620807 | p.Asn306Ile | missense_variant | 0.14 |
rpoB | 759713 | c.-94C>T | upstream_gene_variant | 0.12 |
rpoC | 763079 | c.-291C>T | upstream_gene_variant | 0.12 |
rpoC | 764514 | p.Phe382Ser | missense_variant | 0.25 |
rpoC | 764636 | p.Asp423Tyr | missense_variant | 0.13 |
rpoC | 765277 | c.1908G>T | synonymous_variant | 0.11 |
rpoC | 765302 | p.Glu645Gln | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776080 | p.Ala801Ser | missense_variant | 0.15 |
mmpL5 | 776081 | c.2400G>A | synonymous_variant | 0.15 |
mmpL5 | 779283 | c.-803G>A | upstream_gene_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406282 | c.1059G>A | synonymous_variant | 0.18 |
embR | 1417217 | c.130delA | frameshift_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102944 | c.99C>A | synonymous_variant | 0.12 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.18 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.11 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.11 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290194 | c.-953G>T | upstream_gene_variant | 0.2 |
ribD | 2987451 | c.614_616delGTG | disruptive_inframe_deletion | 0.13 |
rpoA | 3878644 | c.-137G>T | upstream_gene_variant | 1.0 |
clpC1 | 4039971 | p.Lys245Arg | missense_variant | 0.12 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.11 |
clpC1 | 4040311 | p.Thr132Ala | missense_variant | 0.11 |
embC | 4240899 | p.Leu346Pro | missense_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243548 | p.Phe106Leu | missense_variant | 0.12 |
embB | 4248884 | p.Asn791Asp | missense_variant | 0.11 |
aftB | 4267903 | p.Val312Leu | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |