Run ID: ERR4814576
Sample name:
Date: 01-04-2023 13:22:32
Number of reads: 1796714
Percentage reads mapped: 99.31
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 | 1.0 |
rpoB | 760681 | p.Asn292Ser | 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 | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474201 | n.544T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474264 | n.607T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474285 | n.630_631delTC | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474294 | n.637C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474295 | n.638C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474296 | n.640_651delCTCCGGAGGAGG | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474326 | n.669T>A | non_coding_transcript_exon_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168149 | p.Pro822Ser | missense_variant | 1.0 |
PPE35 | 2170400 | c.213G>C | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
clpC1 | 4039729 | p.Asp326Asn | missense_variant | 0.96 |
embA | 4242643 | c.-590C>T | upstream_gene_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 |