Run ID: SRR18003017
Sample name:
Date: 03-04-2023 19:13:56
Number of reads: 4920198
Percentage reads mapped: 99.18
Strain: lineage4.2.2
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 |
lineage4.2 | Euro-American | H;T;LAM | None | 1.0 |
lineage4.2.2 | Euro-American (Ural) | T;LAM7-TUR | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Gly | missense_variant | 1.0 | rifampicin |
rpoB | 761149 | p.Arg448Gln | missense_variant | 1.0 | rifampicin |
fabG1 | 1673432 | c.-8T>A | upstream_gene_variant | 1.0 | isoniazid |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
ethA | 4326921 | c.552dupC | frameshift_variant | 0.99 | ethionamide |
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 |
mshA | 576077 | c.730C>T | synonymous_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.31 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474091 | n.434C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474425 | n.768A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474428 | n.771C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476356 | n.2699C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476384 | n.2727G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.5 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2746607 | p.Ala331Gly | missense_variant | 1.0 |
ribD | 2987196 | p.Val120Ile | missense_variant | 1.0 |
Rv2752c | 3066280 | c.-89C>T | upstream_gene_variant | 1.0 |
ald | 3086742 | c.-78A>C | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612469 | c.648A>G | synonymous_variant | 1.0 |
fbiA | 3640645 | p.Ser35Ala | missense_variant | 1.0 |
alr | 3841567 | c.-147A>G | upstream_gene_variant | 1.0 |
clpC1 | 4039566 | p.Val380Ala | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.11 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.14 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.17 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.21 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |