Run ID: ERR2041693
Sample name:
Date: 27-03-2023 11:47:54
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.1.2.1
Drug-resistance: MDR-TB
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 |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 1.0 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
embB | 4247730 | p.Gly406Ala | missense_variant | 1.0 | ethambutol |
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 |
ccsA | 620006 | p.Val39Ala | missense_variant | 0.11 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoB | 761131 | p.Gly442Val | missense_variant | 0.12 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.97 |
rpoC | 765561 | p.Val731Ala | missense_variant | 0.1 |
rpoC | 766487 | p.Pro1040Ser | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777943 | p.Pro180Thr | missense_variant | 0.1 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406943 | c.397_398insGC | frameshift_variant | 0.12 |
Rv1258c | 1406946 | p.Ala132Gly | missense_variant | 0.12 |
Rv1258c | 1406948 | c.391_392delGC | frameshift_variant | 0.12 |
Rv1258c | 1406990 | c.351C>T | synonymous_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473839 | n.182G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473894 | n.237T>C | non_coding_transcript_exon_variant | 0.11 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.16 |
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 |
ribD | 2987418 | p.Gly194Cys | missense_variant | 0.14 |
thyX | 3067211 | c.735G>A | synonymous_variant | 0.1 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiA | 3640390 | c.-153A>G | upstream_gene_variant | 1.0 |
fbiB | 3642586 | p.Met351Thr | missense_variant | 0.17 |
embC | 4240674 | p.Gly271Val | missense_variant | 0.14 |
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 |
gid | 4408029 | c.174C>G | synonymous_variant | 1.0 |