Run ID: ERR2513773
Sample name:
Date: 31-03-2023 19:53:48
Number of reads: 419756
Percentage reads mapped: 99.59
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 | 0.99 |
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 |
gyrA | 9569 | c.2268C>T | synonymous_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 1.0 |
mshA | 575423 | p.Arg26Cys | missense_variant | 1.0 |
mshA | 575679 | p.Asn111Ser | missense_variant | 1.0 |
mshA | 576702 | c.1355_1356insT | frameshift_variant | 0.29 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.33 |
rpoB | 760115 | c.309C>T | synonymous_variant | 1.0 |
rpoC | 763863 | p.Gln165Pro | missense_variant | 0.2 |
rpoC | 763892 | c.527delA | frameshift_variant | 0.25 |
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 | 1303822 | p.Lys298Glu | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473302 | n.1457G>A | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674776 | p.Gly192Asp | missense_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154019 | p.Phe698Ser | missense_variant | 0.11 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
thyA | 3074371 | p.Met34Thr | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474302 | p.Ala99Gly | missense_variant | 0.17 |
fprA | 3474305 | c.299_300insA | frameshift_variant | 0.18 |
fbiB | 3642079 | p.Pro182Leu | missense_variant | 0.14 |
rpoA | 3878072 | p.Tyr146His | missense_variant | 0.11 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.15 |
clpC1 | 4040447 | p.Lys86Asn | missense_variant | 0.11 |
panD | 4044317 | c.-36A>T | upstream_gene_variant | 0.14 |
embC | 4240464 | p.Phe201Tyr | missense_variant | 0.14 |
embC | 4241012 | p.Met384Val | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 1.0 |
embB | 4247094 | p.Gly194Glu | missense_variant | 0.17 |
embB | 4247280 | p.Phe256Ser | missense_variant | 0.17 |
embB | 4248526 | c.2013C>A | synonymous_variant | 0.11 |
ethA | 4326960 | p.Asp172Asn | missense_variant | 0.18 |
ethA | 4327584 | c.-111A>T | upstream_gene_variant | 0.15 |
ethA | 4327737 | c.-264G>A | upstream_gene_variant | 0.11 |
ethR | 4328102 | c.555_560delGTCATT | disruptive_inframe_deletion | 0.15 |
ethR | 4328111 | p.Ala188Gly | missense_variant | 0.16 |
ethR | 4328113 | c.565_566insAATGAC | stop_gained&disruptive_inframe_insertion | 0.16 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |