Run ID: ERR4819202
Sample name:
Date: 01-04-2023 15:58:49
Number of reads: 851364
Percentage reads mapped: 99.57
Strain: lineage4.8
Drug-resistance: Other
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 |
---|---|---|---|---|---|
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5255 | p.Lys6Glu | missense_variant | 0.22 |
gyrB | 5511 | p.Ser91Phe | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8730 | p.Gly477Arg | missense_variant | 0.13 |
gyrA | 9619 | p.Glu773Gly | missense_variant | 0.22 |
rpoB | 759689 | c.-118A>G | upstream_gene_variant | 0.12 |
rpoC | 766177 | c.2809delA | frameshift_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776249 | c.2232A>G | synonymous_variant | 0.12 |
mmpL5 | 777371 | c.1110C>T | synonymous_variant | 0.12 |
mmpL5 | 778585 | c.-105C>G | upstream_gene_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781654 | c.96delT | frameshift_variant | 0.13 |
fbiC | 1303296 | c.366T>C | synonymous_variant | 0.11 |
fbiC | 1303378 | p.Arg150Ser | missense_variant | 0.11 |
fbiC | 1305232 | p.Ala768Thr | missense_variant | 0.15 |
embR | 1417379 | c.-33_-32insC | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
inhA | 1673952 | c.-250G>A | upstream_gene_variant | 0.11 |
rpsA | 1834628 | p.Lys363Glu | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154072 | c.2040C>T | synonymous_variant | 0.2 |
katG | 2155059 | p.Trp351Cys | missense_variant | 0.22 |
Rv1979c | 2222522 | p.Lys215Glu | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518089 | c.-25delA | upstream_gene_variant | 0.15 |
ahpC | 2726252 | c.60C>T | synonymous_variant | 0.14 |
ahpC | 2726666 | c.474C>T | synonymous_variant | 0.13 |
ribD | 2987110 | p.Glu91Val | missense_variant | 0.11 |
Rv2752c | 3066321 | c.-130C>G | upstream_gene_variant | 1.0 |
thyA | 3074103 | c.369C>A | synonymous_variant | 0.12 |
whiB7 | 3568475 | p.Glu69Lys | missense_variant | 0.12 |
Rv3236c | 3613041 | c.76C>A | synonymous_variant | 0.13 |
clpC1 | 4038326 | p.Glu793Asp | missense_variant | 0.15 |
clpC1 | 4040399 | c.305delA | frameshift_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4267149 | p.Glu563Gly | missense_variant | 1.0 |
aftB | 4267155 | p.Gln561Arg | missense_variant | 1.0 |
ubiA | 4269517 | p.Ala106Val | missense_variant | 0.25 |
ethA | 4326996 | p.Pro160Ala | missense_variant | 0.17 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338666 | c.-145G>A | upstream_gene_variant | 0.12 |
gid | 4407635 | p.Thr190Ala | missense_variant | 0.12 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |