Run ID: ERR4407470
Sample name:
Date: 01-04-2023 05:45:29
Number of reads: 244743
Percentage reads mapped: 99.58
Strain: lineage4.6.2.2
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.2 | Euro-American | T;LAM | RD726 | 1.0 |
lineage4.6.2.2 | Euro-American (Cameroon) | LAM10-CAM | RD726 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
fabG1 | 1673432 | c.-8T>C | upstream_gene_variant | 1.0 | isoniazid, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5749 | c.510G>A | synonymous_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7762 | p.Pro154Arg | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491027 | p.Asn82Thr | missense_variant | 0.29 |
ccsA | 620748 | c.858T>G | synonymous_variant | 0.33 |
rpoB | 763037 | c.3232delA | frameshift_variant | 0.12 |
rpoC | 766361 | p.Val998Met | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778298 | c.-692C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1304863 | p.Ser645Gly | missense_variant | 0.22 |
Rv1258c | 1406994 | p.Phe116Tyr | missense_variant | 0.11 |
Rv1258c | 1407006 | p.Leu112Arg | missense_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472222 | n.377G>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473022 | n.1177G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473076 | n.1231A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473744 | n.87T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473941 | n.284T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473968 | n.314_315dupGG | non_coding_transcript_exon_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2221746 | c.1416_1418dupCCG | disruptive_inframe_insertion | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2715432 | c.-100C>T | upstream_gene_variant | 0.1 |
eis | 2715436 | c.-104G>A | upstream_gene_variant | 0.11 |
eis | 2715440 | c.-108A>C | upstream_gene_variant | 0.11 |
eis | 2715445 | c.-113C>T | upstream_gene_variant | 0.11 |
eis | 2715447 | c.-115T>A | upstream_gene_variant | 0.11 |
eis | 2715450 | c.-118T>C | upstream_gene_variant | 0.11 |
eis | 2715451 | c.-119C>A | upstream_gene_variant | 0.11 |
eis | 2715454 | c.-122T>G | upstream_gene_variant | 0.11 |
eis | 2715455 | c.-123G>A | upstream_gene_variant | 0.11 |
eis | 2715458 | c.-126T>A | upstream_gene_variant | 0.11 |
eis | 2715460 | c.-128A>G | upstream_gene_variant | 0.11 |
eis | 2715465 | c.-133G>T | upstream_gene_variant | 0.12 |
eis | 2715469 | c.-137T>C | upstream_gene_variant | 0.12 |
eis | 2715473 | c.-141A>G | upstream_gene_variant | 0.12 |
ahpC | 2726338 | p.Val49Gly | missense_variant | 0.25 |
ahpC | 2726626 | p.Gln145Arg | missense_variant | 0.18 |
thyX | 3067246 | c.699delC | frameshift_variant | 0.5 |
thyX | 3067474 | p.Pro158Ala | missense_variant | 1.0 |
ald | 3086792 | c.-28G>T | upstream_gene_variant | 0.12 |
fbiD | 3339273 | c.156T>G | synonymous_variant | 0.22 |
fbiD | 3339441 | c.324C>A | synonymous_variant | 0.17 |
Rv3083 | 3448567 | p.His22Asp | missense_variant | 1.0 |
Rv3083 | 3448965 | c.462C>A | synonymous_variant | 0.29 |
Rv3083 | 3449589 | c.1086C>T | synonymous_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4039594 | p.Arg371Gly | missense_variant | 0.12 |
panD | 4043978 | p.Gln102Lys | missense_variant | 0.11 |
embC | 4239732 | c.-131T>C | upstream_gene_variant | 0.11 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.22 |
embC | 4240766 | c.904C>A | synonymous_variant | 0.15 |
embC | 4240828 | c.968delC | frameshift_variant | 0.11 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
aftB | 4267272 | p.Lys522Arg | missense_variant | 1.0 |
ethR | 4326739 | c.-810G>C | upstream_gene_variant | 1.0 |
ethA | 4328004 | c.-531C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |