Run ID: ERR1750881
Sample name:
Date: 31-03-2023 14:58:06
Number of reads: 4115159
Percentage reads mapped: 94.51
Strain: lineage4.1.1.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 1.0 |
lineage4.1.1.3 | Euro-American (X-type) | X1;X3 | RD193 | 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 | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781435 | c.-125G>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471929 | n.84C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1471930 | n.85G>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1471992 | n.147A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472221 | n.376G>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472230 | n.385C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474548 | n.891T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475080 | n.1423G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475081 | n.1424C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475969 | n.2312T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.98 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407798 | c.405G>T | synonymous_variant | 1.0 |