Run ID: ERR4817975
Sample name:
Date: 01-04-2023 15:17:44
Number of reads: 2469284
Percentage reads mapped: 99.47
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 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475504 | n.1847C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475989 | n.2332T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475990 | n.2333G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.6 |
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 |
thyA | 3073929 | c.543T>C | synonymous_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086987 | p.Gln56His | missense_variant | 0.21 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.96 |
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 |