Run ID: ERR1213918
Sample name:
Date: 31-03-2023 12:44:15
Number of reads: 1862677
Percentage reads mapped: 99.02
Strain: lineage4.6.2
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.6 | Euro-American | T;LAM | None | 0.83 |
lineage4.6.2 | Euro-American | T;LAM | RD726 | 0.85 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
fabG1 | 1673425 | c.-15C>T | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5325 | p.Arg29Leu | missense_variant | 0.2 |
gyrB | 7196 | p.Gly653Cys | missense_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7892 | c.591G>A | synonymous_variant | 0.17 |
gyrA | 8397 | p.Val366Ile | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoB | 759939 | p.Pro45Ala | missense_variant | 0.71 |
rpoC | 762836 | c.-534C>G | upstream_gene_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776683 | c.1798C>T | synonymous_variant | 0.22 |
mmpL5 | 777647 | c.834C>A | synonymous_variant | 0.33 |
mmpR5 | 778298 | c.-692C>T | upstream_gene_variant | 0.94 |
fbiC | 1304723 | p.Glu598Val | missense_variant | 0.29 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472487 | n.643dupT | non_coding_transcript_exon_variant | 0.82 |
rrl | 1473752 | n.95G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474028 | n.371T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474029 | n.372G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474034 | n.377G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474040 | n.383G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476716 | n.3059A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476726 | n.3069A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476746 | n.3089T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476755 | n.3098G>T | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834118 | p.Gln193* | stop_gained | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2155389 | c.723C>G | synonymous_variant | 1.0 |
PPE35 | 2168499 | p.Ser705Leu | missense_variant | 0.12 |
PPE35 | 2169320 | p.Leu431Phe | missense_variant | 0.54 |
PPE35 | 2169785 | p.Asn276Lys | missense_variant | 0.12 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 0.6 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714130 | p.Glu401Asp | missense_variant | 0.25 |
eis | 2714320 | p.Ala338Val | missense_variant | 0.25 |
eis | 2714727 | c.606A>C | synonymous_variant | 0.71 |
thyX | 3067474 | p.Pro158Ala | missense_variant | 0.67 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.15 |
Rv3083 | 3448394 | c.-110G>T | upstream_gene_variant | 0.29 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 0.64 |
Rv3083 | 3449882 | p.Trp460* | stop_gained | 0.17 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612571 | c.546C>T | synonymous_variant | 1.0 |
Rv3236c | 3612768 | p.Ala117Ser | missense_variant | 0.25 |
alr | 3840904 | p.Pro173Ser | missense_variant | 0.18 |
embC | 4242075 | p.Arg738Gln | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247613 | p.Arg367His | missense_variant | 0.25 |
embB | 4247973 | p.Thr487Ile | missense_variant | 0.22 |
embB | 4248298 | c.1785C>T | synonymous_variant | 0.5 |
embB | 4248964 | c.2451G>A | synonymous_variant | 0.33 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 0.93 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 0.75 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 0.62 |
ethA | 4328202 | c.-729G>A | upstream_gene_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 0.4 |