Run ID: ERR4817508
Sample name:
Date: 01-04-2023 15:02:03
Number of reads: 1212792
Percentage reads mapped: 97.64
Strain: lineage4.1.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | 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 |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.36 | streptomycin |
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 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.35 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.3 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761642 | c.1836G>C | synonymous_variant | 1.0 |
rpoB | 761643 | p.Val613Phe | 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 |
fbiC | 1304415 | c.1485G>A | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472655 | n.810G>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472687 | n.843dupT | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.11 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.24 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.25 |
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 |
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 |