Run ID: ERR9993029
Sample name:
Date: 02-04-2023 14:00:31
Number of reads: 2542950
Percentage reads mapped: 75.24
Strain: lineage4.3.3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761161 | p.Leu452Pro | missense_variant | 1.0 | rifampicin |
fabG1 | 1673432 | c.-8T>A | upstream_gene_variant | 1.0 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288785 | c.456dupC | frameshift_variant | 0.99 | pyrazinamide, pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4327484 | c.-11A>G | upstream_gene_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.34 |
rpoB | 762889 | p.His1028Arg | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778994 | p.Ser2Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472222 | n.377G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472229 | n.384C>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472708 | n.863T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472733 | n.888G>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472742 | n.897C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472982 | n.1137G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473001 | n.1156G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473002 | n.1157G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473008 | n.1163C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473009 | n.1164T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223051 | p.Glu38Asp | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
Rv2752c | 3065824 | p.Pro123Leu | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878583 | c.-76C>A | upstream_gene_variant | 0.25 |
rpoA | 3878609 | c.-102T>A | upstream_gene_variant | 0.27 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.98 |
gid | 4407912 | c.160_290del | frameshift_variant | 1.0 |