Run ID: ERR4816120
Sample name:
Date: 01-04-2023 14:15:17
Number of reads: 4081669
Percentage reads mapped: 99.26
Strain: lineage4.1.3
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 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.3 | Euro-American | T;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761139 | p.His445Tyr | missense_variant | 1.0 | rifampicin |
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9557 | c.2256G>C | synonymous_variant | 1.0 |
rpoB | 760295 | p.Asn163Lys | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 1.0 |
fbiC | 1304610 | c.1680C>T | synonymous_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475395 | n.1740_1741delGC | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.99 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289051 | p.Tyr64Ser | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |