Run ID: ERR4818499
Sample name:
Date: 01-04-2023 15:35:28
Number of reads: 2273
Percentage reads mapped: 16.09
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpsL | 781841 | c.282C>T | synonymous_variant | 1.0 |
rpsL | 781857 | p.Gly100Cys | missense_variant | 1.0 |
rpsL | 781865 | c.306G>C | synonymous_variant | 1.0 |
rpsL | 781868 | c.309T>C | synonymous_variant | 1.0 |
rpsL | 781871 | c.312G>C | synonymous_variant | 1.0 |
rpsL | 781892 | c.333A>G | synonymous_variant | 1.0 |
rpsL | 781898 | c.339A>T | synonymous_variant | 1.0 |
rpsL | 781907 | c.348T>C | synonymous_variant | 1.0 |
rpsL | 781913 | c.354C>A | synonymous_variant | 1.0 |
rpsL | 781916 | c.357T>C | synonymous_variant | 1.0 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 1.0 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 1.0 |
clpC1 | 4039950 | p.Leu252Pro | missense_variant | 1.0 |