Run ID: ERR4815365
Sample name:
Date: 01-04-2023 13:49:31
Number of reads: 2375010
Percentage reads mapped: 99.63
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.98 |
mshA | 576586 | c.1239G>A | synonymous_variant | 0.97 |
rpoB | 759615 | c.-192A>C | upstream_gene_variant | 0.19 |
rpoC | 763555 | c.186C>T | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpS5 | 779601 | c.-696A>C | upstream_gene_variant | 1.0 |
rpsL | 781383 | c.-177G>C | upstream_gene_variant | 0.99 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472592 | n.747C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.543A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.98 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746970 | p.Ala210Val | missense_variant | 0.99 |
Rv3083 | 3448322 | c.-182G>A | upstream_gene_variant | 0.98 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4326169 | c.1305C>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |