Run ID: ERR2229113
Sample name:
Date: 31-03-2023 16:40:03
Number of reads: 443014
Percentage reads mapped: 99.42
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 | 2155345 | c.766delG | frameshift_variant | 0.17 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.15 |
fgd1 | 491034 | c.252C>A | synonymous_variant | 0.17 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.36 |
mshA | 576111 | p.Ala255Gly | missense_variant | 0.29 |
rpoC | 767124 | p.Val1252Glu | missense_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.14 |
mmpL5 | 777164 | c.1317C>T | synonymous_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800862 | c.54C>T | synonymous_variant | 0.2 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471915 | n.70C>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473552 | n.-106G>T | upstream_gene_variant | 0.5 |
rrl | 1475476 | n.1819G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476274 | n.2617G>T | non_coding_transcript_exon_variant | 0.22 |
fabG1 | 1673346 | c.-94C>G | upstream_gene_variant | 0.17 |
fabG1 | 1673349 | c.-91G>C | upstream_gene_variant | 0.18 |
fabG1 | 1673359 | c.-81T>C | upstream_gene_variant | 0.11 |
fabG1 | 1673361 | c.-79C>G | upstream_gene_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.18 |
inhA | 1674691 | p.Ala164Thr | missense_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154582 | c.1530C>T | synonymous_variant | 0.2 |
katG | 2154877 | p.Trp412Leu | missense_variant | 0.29 |
katG | 2155204 | p.Ser303* | stop_gained | 0.29 |
PPE35 | 2167965 | c.2646_2647delAG | frameshift_variant | 0.33 |
PPE35 | 2167973 | c.2640A>G | synonymous_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169732 | p.Asn294Ser | missense_variant | 0.12 |
PPE35 | 2169749 | c.864A>T | synonymous_variant | 0.13 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.2 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.19 |
PPE35 | 2170528 | p.Ser29Ala | missense_variant | 0.15 |
PPE35 | 2170529 | c.84G>C | synonymous_variant | 0.15 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518606 | c.492G>C | synonymous_variant | 0.17 |
pepQ | 2860026 | c.393G>A | synonymous_variant | 0.18 |
Rv2752c | 3065275 | p.Gly306Ala | missense_variant | 0.22 |
Rv2752c | 3065519 | p.Leu225Ile | missense_variant | 0.15 |
ald | 3086680 | c.-139delT | upstream_gene_variant | 0.22 |
Rv3236c | 3612107 | c.1009delT | frameshift_variant | 0.15 |
Rv3236c | 3612277 | c.840G>A | synonymous_variant | 0.17 |
clpC1 | 4038835 | p.Phe624Ile | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244693 | c.1461C>T | synonymous_variant | 0.22 |
embB | 4246187 | c.-327C>T | upstream_gene_variant | 0.2 |
embB | 4246894 | c.381C>T | synonymous_variant | 0.2 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.29 |
embB | 4247516 | p.Asn335Asp | missense_variant | 0.29 |
embB | 4249532 | p.Ala1007Thr | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-6_*1418del | transcript_ablation | 1.0 |