Run ID: ERR2515027
Sample name:
Date: 31-03-2023 20:42:39
Number of reads: 2028419
Percentage reads mapped: 99.36
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 | 0.99 |
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 | 781633 | p.Lys25Thr | missense_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474637 | n.980C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476149 | n.2492C>A | non_coding_transcript_exon_variant | 0.25 |
tlyA | 1917972 | c.33A>G | 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 |