Run ID: ERR2041702
Sample name:
Date: 18-08-2022 09:23:30
Number of reads: 519869
Percentage reads mapped: 98.64
Strain: lineage4.7
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 |
lineage4.7 | Euro-American (mainly T) | T1;T5 | None | 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 |
pncA | 2288835 | c.395_406delGTATTGCCACCG | disruptive_inframe_deletion | 1.0 | pyrazinamide |
embB | 4247429 | p.Met306Val | missense_variant | 1.0 | ethambutol |
ethA | 4326721 | c.752dupG | frameshift_variant | 1.0 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6358 | c.-944C>T | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoB | 762433 | p.Gly876Asp | missense_variant | 0.13 |
rpoB | 762777 | p.Asp991Asn | missense_variant | 0.18 |
rpoC | 764004 | p.Ala212Val | missense_variant | 0.14 |
rpoC | 764916 | p.Leu516Pro | missense_variant | 1.0 |
mmpR5 | 779034 | c.46_47delAT | frameshift_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471778 | n.-68G>C | upstream_gene_variant | 1.0 |
rrs | 1471895 | n.50C>G | non_coding_transcript_exon_variant | 0.1 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472033 | n.188A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472362 | n.517C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474294 | n.637C>G | non_coding_transcript_exon_variant | 1.0 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.19 |
rpsA | 1834900 | c.1359C>T | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154468 | c.1644C>G | synonymous_variant | 0.1 |
pncA | 2290005 | c.-764G>T | upstream_gene_variant | 0.12 |
embC | 4239984 | p.Ala41Val | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244772 | p.Ser514Thr | missense_variant | 0.17 |
embA | 4245445 | p.Asp738Val | missense_variant | 0.11 |
embB | 4246070 | c.-444G>T | upstream_gene_variant | 0.15 |
embB | 4249732 | c.3219C>G | synonymous_variant | 1.0 |
ubiA | 4269012 | c.822G>A | synonymous_variant | 0.12 |
ubiA | 4269323 | p.Pro171Ser | missense_variant | 1.0 |
ubiA | 4269747 | c.86dupA | frameshift_variant | 0.12 |
gid | 4407980 | p.Pro75Ser | missense_variant | 1.0 |
mshA | 574786 | c.-561_*636del | transcript_ablation | 1.0 |