Run ID: ERR2229181
Sample name:
Date: 31-03-2023 16:47:28
Number of reads: 803526
Percentage reads mapped: 99.37
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 | 6798 | p.Gly520Asp | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 760753 | p.Leu316Pro | missense_variant | 0.1 |
rpoB | 761285 | c.1479G>A | synonymous_variant | 0.22 |
rpoC | 763887 | p.Arg173Leu | missense_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305049 | p.Thr707Ser | missense_variant | 0.17 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471881 | n.36A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473264 | n.1419A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.12 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.23 |
rpsA | 1834914 | p.Lys458Arg | missense_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168585 | c.2028T>C | synonymous_variant | 0.17 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.48 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.46 |
PPE35 | 2170540 | c.73C>T | synonymous_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289367 | c.-126C>A | upstream_gene_variant | 0.12 |
kasA | 2518508 | p.Gly132Cys | missense_variant | 0.2 |
kasA | 2518791 | p.Ala226Val | missense_variant | 0.22 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.17 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.15 |
kasA | 2519140 | c.1026G>C | synonymous_variant | 0.17 |
kasA | 2519143 | c.1029G>C | synonymous_variant | 0.17 |
ahpC | 2725923 | c.-270A>T | upstream_gene_variant | 0.13 |
folC | 2747005 | p.Ser198Arg | missense_variant | 0.14 |
ald | 3087260 | p.Tyr147* | stop_gained | 0.22 |
fbiD | 3339739 | p.Ala208Pro | missense_variant | 0.25 |
fbiB | 3642216 | p.Thr228Ser | missense_variant | 0.13 |
fbiB | 3642595 | p.Pro354Leu | missense_variant | 0.13 |
clpC1 | 4039497 | p.Ile403Asn | missense_variant | 0.22 |
clpC1 | 4040037 | p.Thr223Ile | missense_variant | 0.12 |
embC | 4240502 | p.Phe214Val | missense_variant | 0.18 |
embC | 4241760 | p.Ser633Leu | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.5 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.5 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.67 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.67 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.67 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.8 |
ubiA | 4269577 | c.256delA | frameshift_variant | 0.1 |
ubiA | 4270029 | c.-196G>A | upstream_gene_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1408del | transcript_ablation | 1.0 |