Run ID: ERR9787000
Sample name:
Date: 02-04-2023 12:56:15
Number of reads: 3431596
Percentage reads mapped: 91.06
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
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 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
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 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471685 | n.-161A>G | upstream_gene_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473091 | n.1246G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473120 | n.1275C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.1 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101737 | p.Ala436Thr | missense_variant | 1.0 |
ndh | 2101931 | p.Ala371Val | missense_variant | 1.0 |
katG | 2156554 | c.-443G>A | upstream_gene_variant | 1.0 |
PPE35 | 2169734 | c.879C>A | synonymous_variant | 1.0 |
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 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |