Run ID: ERR4814813
Sample name:
Date: 01-04-2023 13:30:14
Number of reads: 1775348
Percentage reads mapped: 97.92
Strain: lineage4.3.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.1 | Euro-American (LAM) | LAM9 | None | 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 | 7464 | c.164delT | frameshift_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.12 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.13 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.12 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.12 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.12 |
rpsL | 781856 | c.297C>T | synonymous_variant | 0.14 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.13 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.1 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472674 | n.829T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472681 | n.836C>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472685 | n.840G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472791 | n.946G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472793 | n.948A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2168412 | p.Phe734Cys | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039367 | p.Lys446Asn | missense_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4328103 | c.-630C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |