Run ID: ERR2229678
Sample name:
Date: 31-03-2023 17:24:44
Number of reads: 661881
Percentage reads mapped: 99.61
Strain: lineage4.8
Drug-resistance: HR-TB
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 |
---|---|---|---|---|---|
katG | 2154014 | p.Ser700Pro | missense_variant | 0.22 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
fgd1 | 491776 | c.994T>C | synonymous_variant | 0.12 |
mshA | 576441 | p.Cys365Phe | missense_variant | 0.1 |
mshA | 576771 | p.Arg475Leu | missense_variant | 0.11 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.17 |
rpoB | 759954 | p.Val50Ile | missense_variant | 0.11 |
rpoB | 759972 | p.Glu56Lys | missense_variant | 0.12 |
rpoB | 761259 | p.Gly485Trp | missense_variant | 0.17 |
rpoC | 763526 | p.Gly53Trp | missense_variant | 0.11 |
rpoC | 763852 | c.483C>A | synonymous_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777396 | p.Ser362Ile | missense_variant | 0.22 |
mmpL5 | 777478 | p.Leu335Phe | missense_variant | 0.17 |
mmpR5 | 779158 | p.Ala57Leu | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304109 | c.1179C>T | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473737 | n.80G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.1 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.1 |
fabG1 | 1673560 | p.Lys41Leu | missense_variant | 0.15 |
rpsA | 1834859 | p.Ala440Pro | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101813 | p.Lys410Asn | missense_variant | 0.18 |
ndh | 2101981 | c.1062C>A | synonymous_variant | 0.12 |
ndh | 2103225 | c.-183A>C | upstream_gene_variant | 0.31 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169991 | p.Gly208Cys | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518375 | c.261C>A | synonymous_variant | 0.12 |
kasA | 2518683 | p.Ala190Val | missense_variant | 0.15 |
kasA | 2518686 | p.Asp191Gly | missense_variant | 0.17 |
kasA | 2519057 | p.Thr315Ser | missense_variant | 0.15 |
kasA | 2519061 | p.Pro316Arg | missense_variant | 0.18 |
kasA | 2519078 | p.Glu322Leu | missense_variant | 0.29 |
kasA | 2519083 | c.970_976delAACGCCA | frameshift_variant | 0.33 |
kasA | 2519097 | p.Val328Gly | missense_variant | 0.33 |
pepQ | 2859707 | p.Val238Leu | missense_variant | 0.11 |
Rv2752c | 3064534 | p.Pro553Leu | missense_variant | 0.17 |
thyX | 3067529 | c.417C>A | synonymous_variant | 0.14 |
thyX | 3067748 | c.198C>T | synonymous_variant | 0.1 |
thyA | 3074259 | p.Trp71Cys | missense_variant | 0.1 |
ald | 3086938 | p.Gly40Val | missense_variant | 0.1 |
fbiD | 3339078 | c.-40C>A | upstream_gene_variant | 0.14 |
Rv3236c | 3612060 | p.Ala353Thr | missense_variant | 0.11 |
Rv3236c | 3612504 | p.His205Tyr | missense_variant | 0.11 |
fbiB | 3641997 | p.Ala155Ser | missense_variant | 0.25 |
alr | 3840882 | p.Arg180Leu | missense_variant | 0.17 |
rpoA | 3878069 | p.Val147Ile | missense_variant | 0.1 |
clpC1 | 4038752 | p.Gln651His | missense_variant | 0.1 |
clpC1 | 4039321 | p.Ala462Ser | missense_variant | 0.11 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.13 |
clpC1 | 4040172 | p.Leu178His | missense_variant | 0.2 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.25 |
embC | 4241034 | p.Pro391Gln | missense_variant | 0.22 |
embC | 4241538 | p.Gly559Asp | missense_variant | 1.0 |
embC | 4241549 | p.Gly563* | stop_gained | 0.14 |
embC | 4241658 | p.Ser599* | stop_gained | 0.2 |
embC | 4242230 | p.Ile790Leu | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4267233 | p.Asp535Val | missense_variant | 0.11 |
whiB6 | 4338395 | p.Thr43Ala | missense_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |