Run ID: ERR5917706
Sample name:
Date: 02-04-2023 00:56:59
Number of reads: 2357348
Percentage reads mapped: 99.5
Strain: lineage4.1.2
Drug-resistance: Other
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 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289089 | p.His51Gln | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5959 | c.720C>G | synonymous_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 576766 | c.1419G>A | synonymous_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 763555 | c.186C>T | synonymous_variant | 1.0 |
rpoC | 764634 | p.Val422Ala | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 778134 | c.345_346delAC | frameshift_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303434 | p.Asp168Glu | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474092 | n.435G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474549 | n.892G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476026 | n.2369T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2169041 | c.1572G>A | synonymous_variant | 0.44 |
PPE35 | 2169053 | c.1560T>C | synonymous_variant | 1.0 |
PPE35 | 2169059 | c.1554G>A | synonymous_variant | 0.89 |
PPE35 | 2169063 | p.Met517Thr | missense_variant | 1.0 |
PPE35 | 2169065 | p.Ala516Thr | missense_variant | 0.89 |
PPE35 | 2169068 | c.1545G>T | synonymous_variant | 0.89 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_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 |
embB | 4246567 | c.54G>T | synonymous_variant | 1.0 |
embB | 4246584 | p.Arg24Pro | missense_variant | 0.24 |
embB | 4248551 | p.Ala680Thr | missense_variant | 1.0 |
aftB | 4267099 | p.Ala580Ser | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408082 | p.Val41Ile | missense_variant | 1.0 |