Run ID: ERR4814989
Sample name:
Date: 01-04-2023 13:36:23
Number of reads: 694584
Percentage reads mapped: 98.69
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 | 8763 | p.Asp488Tyr | missense_variant | 0.5 |
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 | 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 |
embR | 1417140 | p.Ala70Ser | missense_variant | 0.12 |
atpE | 1461275 | c.231T>C | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473706 | n.49A>C | non_coding_transcript_exon_variant | 0.18 |
inhA | 1673565 | c.-637G>T | upstream_gene_variant | 0.25 |
tlyA | 1917902 | c.-38G>T | upstream_gene_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102132 | p.Gln304Arg | missense_variant | 0.22 |
PPE35 | 2167792 | p.Ser941Ala | missense_variant | 1.0 |
PPE35 | 2170119 | p.Leu165Arg | missense_variant | 0.33 |
PPE35 | 2170148 | p.His155Gln | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
ahpC | 2725992 | c.-201G>C | upstream_gene_variant | 1.0 |
folC | 2747581 | c.18C>T | synonymous_variant | 0.2 |
folC | 2747668 | c.-70A>C | upstream_gene_variant | 0.33 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448907 | p.Tyr135Ser | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640366 | c.-177G>A | upstream_gene_variant | 1.0 |
embC | 4239776 | c.-87G>T | upstream_gene_variant | 0.2 |
embC | 4240569 | p.Leu236Arg | missense_variant | 0.33 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embA | 4245146 | p.Gln638His | missense_variant | 0.18 |
embA | 4245934 | p.Pro901Leu | missense_variant | 0.2 |
aftB | 4268709 | p.Ala43Val | missense_variant | 0.15 |
ethA | 4326420 | p.Ala352Thr | missense_variant | 0.16 |
ethA | 4327269 | p.Trp69Gly | missense_variant | 0.21 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |