Run ID: ERR279587
Sample name:
Date: 31-03-2023 23:41:58
Number of reads: 201231
Percentage reads mapped: 96.76
Strain: lineage4.9;lineage2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.08 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 9005 | c.1704G>T | synonymous_variant | 0.5 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620660 | p.Arg257His | missense_variant | 1.0 |
mmpL5 | 775853 | c.2627_2628insT | frameshift_variant | 0.67 |
Rv1258c | 1406228 | c.1113C>T | synonymous_variant | 1.0 |
rrs | 1471713 | n.-133G>T | upstream_gene_variant | 1.0 |
rrs | 1471758 | n.-88G>T | upstream_gene_variant | 0.5 |
rrs | 1471873 | n.28C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473208 | n.1365_1366delTG | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473392 | n.-266C>A | upstream_gene_variant | 0.67 |
rrl | 1474290 | n.633T>C | non_coding_transcript_exon_variant | 1.0 |
inhA | 1673816 | c.-386G>A | upstream_gene_variant | 0.67 |
fabG1 | 1674152 | p.Pro238Gln | missense_variant | 0.5 |
ndh | 2103116 | c.-74C>A | upstream_gene_variant | 0.67 |
PPE35 | 2169997 | p.Ser206Cys | missense_variant | 0.5 |
PPE35 | 2170561 | p.Gly18Arg | missense_variant | 0.4 |
Rv1979c | 2221812 | c.1353G>A | synonymous_variant | 1.0 |
Rv1979c | 2223220 | c.-56G>A | upstream_gene_variant | 1.0 |
kasA | 2518589 | p.Gly159Arg | missense_variant | 0.67 |
eis | 2715122 | p.Val71Met | missense_variant | 0.4 |
thyX | 3067909 | p.Ala13Thr | missense_variant | 0.67 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339303 | c.186C>T | synonymous_variant | 1.0 |
fprA | 3475152 | p.Leu382Phe | missense_variant | 0.67 |
rpoA | 3877963 | p.Arg182Pro | missense_variant | 1.0 |
rpoA | 3878132 | p.Ala126Thr | missense_variant | 1.0 |
embC | 4240088 | p.Gly76Arg | missense_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.75 |
embA | 4245881 | p.Asp883Glu | missense_variant | 1.0 |
embB | 4248481 | p.Phe656Leu | missense_variant | 0.5 |
aftB | 4268589 | p.Ala83Val | missense_variant | 0.4 |
ethA | 4326424 | c.1050T>G | synonymous_variant | 1.0 |
ethA | 4326633 | p.His281Tyr | missense_variant | 0.5 |
ethA | 4328291 | c.-818C>T | upstream_gene_variant | 0.67 |
ethA | 4328303 | c.-831delA | upstream_gene_variant | 0.67 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |