Run ID: ERR4817754
Sample name:
Date: 01-04-2023 15:10:29
Number of reads: 286032
Percentage reads mapped: 92.28
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 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 | 491014 | p.Thr78Pro | missense_variant | 0.22 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.33 |
ccsA | 620380 | p.Met164Val | missense_variant | 0.33 |
rpoB | 759898 | p.Asn31Thr | missense_variant | 0.18 |
rpoB | 761835 | p.Cys677Arg | missense_variant | 0.29 |
rpoC | 765727 | c.2358T>C | synonymous_variant | 0.29 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776092 | p.Ser797Cys | missense_variant | 0.18 |
mmpL5 | 776287 | p.Ile732Val | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
fabG1 | 1674076 | p.Thr213Pro | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102540 | p.Ala168Gly | missense_variant | 0.25 |
ndh | 2102623 | c.420C>T | synonymous_variant | 0.18 |
katG | 2155895 | p.Val73Ile | missense_variant | 0.15 |
katG | 2156045 | p.Val23Leu | missense_variant | 1.0 |
PPE35 | 2167898 | c.2715G>C | synonymous_variant | 0.17 |
PPE35 | 2167901 | c.2712T>C | synonymous_variant | 0.17 |
PPE35 | 2168304 | p.Thr770Met | missense_variant | 0.18 |
PPE35 | 2169488 | c.1125G>C | synonymous_variant | 0.2 |
PPE35 | 2169491 | c.1122T>C | synonymous_variant | 0.2 |
Rv1979c | 2221889 | p.Val426Ile | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715036 | c.297G>A | synonymous_variant | 0.13 |
Rv2752c | 3065090 | p.Ala368Ser | missense_variant | 0.14 |
thyX | 3067986 | c.-42delC | upstream_gene_variant | 0.29 |
thyX | 3068115 | c.-170C>T | upstream_gene_variant | 0.25 |
ald | 3086634 | c.-186T>C | upstream_gene_variant | 0.13 |
fbiA | 3641129 | p.Ala196Val | missense_variant | 1.0 |
ddn | 3987022 | p.Arg60Pro | missense_variant | 0.2 |
embC | 4239821 | c.-42C>T | upstream_gene_variant | 0.15 |
ethA | 4327061 | p.Ser138Thr | missense_variant | 0.18 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |