Run ID: ERR2503426
Sample name:
Date: 31-03-2023 18:27:13
Number of reads: 338552
Percentage reads mapped: 99.58
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 | 8011 | p.Ser237Phe | missense_variant | 0.11 |
gyrA | 8661 | p.Asp454Asn | missense_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491084 | p.Val101Ala | missense_variant | 0.12 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
ccsA | 620521 | p.Ala211Thr | missense_variant | 0.14 |
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 |
fbiC | 1304826 | c.1900delT | frameshift_variant | 0.14 |
Rv1258c | 1406183 | c.1158C>T | synonymous_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
PPE35 | 2167820 | c.2793G>A | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
kasA | 2518425 | p.Asp104Ala | missense_variant | 0.15 |
kasA | 2518811 | p.Asp233Tyr | missense_variant | 0.18 |
eis | 2714708 | c.624delC | frameshift_variant | 0.1 |
pepQ | 2860419 | c.-1C>T | upstream_gene_variant | 0.12 |
ribD | 2986827 | c.-12G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339565 | p.Val150Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612505 | p.His204Gln | missense_variant | 0.22 |
alr | 3840225 | p.Thr399Asn | missense_variant | 1.0 |
alr | 3841038 | p.Val128Gly | missense_variant | 0.11 |
clpC1 | 4040559 | p.Leu49Gln | missense_variant | 0.11 |
embC | 4240558 | c.696C>T | synonymous_variant | 0.14 |
embC | 4240674 | p.Gly271Val | missense_variant | 0.17 |
embC | 4241753 | p.Ala631Thr | missense_variant | 0.25 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4248965 | p.Pro818Thr | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |