Run ID: ERR2229062
Sample name:
Date: 31-03-2023 16:34:29
Number of reads: 521880
Percentage reads mapped: 99.4
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 | 2155105 | c.1006delC | frameshift_variant | 0.14 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 760008 | p.Ala68Ser | missense_variant | 0.12 |
rpoB | 760606 | p.Ala267Glu | missense_variant | 0.22 |
rpoB | 761850 | p.Pro682Ser | missense_variant | 0.14 |
rpoC | 763702 | c.333C>A | synonymous_variant | 0.2 |
rpoC | 766753 | c.3384C>T | synonymous_variant | 0.17 |
rpoC | 766826 | p.His1153Asn | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775685 | c.2796C>A | synonymous_variant | 0.4 |
mmpL5 | 775688 | c.2793C>A | synonymous_variant | 0.33 |
mmpL5 | 775691 | c.2790G>C | synonymous_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
atpE | 1461224 | c.180T>C | synonymous_variant | 0.16 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471787 | n.-59T>C | upstream_gene_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476454 | n.2797C>T | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.28 |
rpsA | 1834027 | c.486G>A | synonymous_variant | 0.13 |
rpsA | 1834550 | p.Val337Met | missense_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154345 | c.1767C>T | synonymous_variant | 0.15 |
katG | 2156085 | c.27A>G | synonymous_variant | 0.13 |
PPE35 | 2168014 | p.Ala867Ser | missense_variant | 0.15 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.11 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.11 |
PPE35 | 2169337 | p.Asp426His | missense_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.36 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.36 |
PPE35 | 2170235 | c.378T>C | synonymous_variant | 0.1 |
PPE35 | 2170238 | c.375T>G | synonymous_variant | 0.1 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289749 | c.-508G>T | upstream_gene_variant | 0.29 |
ribD | 2987487 | p.Pro217Ser | missense_variant | 0.17 |
thyX | 3067736 | p.Phe70Leu | missense_variant | 0.29 |
ald | 3087467 | p.His216Gln | missense_variant | 0.13 |
Rv3083 | 3448405 | c.-99G>A | upstream_gene_variant | 0.29 |
fprA | 3473808 | c.-199C>A | upstream_gene_variant | 0.12 |
fprA | 3474435 | c.429C>A | synonymous_variant | 0.15 |
Rv3236c | 3612084 | p.Gly345Arg | missense_variant | 0.12 |
Rv3236c | 3612288 | p.Gly277Arg | missense_variant | 0.18 |
fbiA | 3641128 | p.Ala196Ser | missense_variant | 0.14 |
alr | 3840888 | p.Ala178Glu | missense_variant | 0.15 |
rpoA | 3878315 | p.Thr65Ala | missense_variant | 0.12 |
rpoA | 3878366 | p.Gly48* | stop_gained | 0.14 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.11 |
clpC1 | 4040328 | p.Lys126Arg | missense_variant | 0.15 |
panD | 4043907 | c.375C>A | synonymous_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243629 | p.Ala133Ser | missense_variant | 0.22 |
embA | 4245380 | p.Tyr716* | stop_gained | 0.18 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.33 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.38 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.5 |
embB | 4247059 | c.546C>G | synonymous_variant | 0.18 |
embB | 4247060 | p.Pro183Ala | missense_variant | 0.18 |
embB | 4247066 | p.Ile185Val | missense_variant | 0.18 |
embB | 4248778 | c.2265C>G | synonymous_variant | 0.13 |
embB | 4249676 | p.Arg1055Ser | missense_variant | 0.22 |
ethR | 4326961 | c.-588G>C | upstream_gene_variant | 0.12 |
ethA | 4327297 | p.Met59Ile | missense_variant | 0.17 |
ethA | 4327938 | c.-465G>T | upstream_gene_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 |