Run ID: ERR6865787
Sample name:
Date: 02-04-2023 03:05:19
Number of reads: 974928
Percentage reads mapped: 62.04
Strain: lineage4.1.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 1.0 |
lineage4.1.2 | Euro-American | T;H | None | 1.0 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 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 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
rpoB | 760106 | c.300G>A | synonymous_variant | 1.0 |
rpoB | 760115 | c.309C>T | synonymous_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 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476252 | n.2595T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476266 | n.2609G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476281 | n.2624T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476356 | n.2699C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476381 | n.2724G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476384 | n.2727G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476455 | n.2798C>G | non_coding_transcript_exon_variant | 0.1 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641454 | c.-81G>A | upstream_gene_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |