Run ID: ERR4816725
Sample name:
Date: 01-04-2023 14:35:44
Number of reads: 2174884
Percentage reads mapped: 99.15
Strain: lineage4.8
Drug-resistance: Other
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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.22 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoC | 766085 | p.Pro906Ala | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801156 | c.348T>C | synonymous_variant | 1.0 |
atpE | 1460992 | c.-53A>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472668 | n.825_829delGGGTT | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472675 | n.830_831insAGAC | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472680 | n.835C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472683 | n.838T>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472689 | n.844C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473291 | n.1446G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.12 |
rpsA | 1834028 | p.Pro163Ser | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168891 | c.1722A>C | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
fprA | 3474439 | c.434delT | frameshift_variant | 1.0 |
fbiB | 3641895 | c.361C>T | synonymous_variant | 1.0 |
alr | 3840764 | c.657G>C | synonymous_variant | 1.0 |
clpC1 | 4039016 | c.1689C>T | synonymous_variant | 0.98 |
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 |