Run ID: ERR1950000
Sample name:
Date: 18-08-2022 11:13:03
Number of reads: 983845
Percentage reads mapped: 99.34
Strain: lineage4.8
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761101 | p.Gln432Arg | missense_variant | 0.12 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
rpoC | 766689 | p.Val1107Gly | missense_variant | 0.23 |
rpoC | 766701 | p.Leu1111Gln | missense_variant | 0.3 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 801136 | p.Ser110Gly | missense_variant | 0.12 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304996 | p.Leu689Ser | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472538 | n.693A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472977 | n.1132G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473915 | n.258A>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474020 | n.363A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474021 | n.364A>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476562 | n.2905C>G | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673849 | p.Phe137Ser | missense_variant | 0.1 |
inhA | 1674344 | p.Gln48Arg | missense_variant | 0.15 |
rpsA | 1834518 | p.Leu326Arg | missense_variant | 0.25 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
pncA | 2289761 | c.-520A>C | upstream_gene_variant | 0.18 |
ahpC | 2725935 | c.-258G>T | upstream_gene_variant | 0.16 |
ahpC | 2726536 | p.Lys115Arg | missense_variant | 0.12 |
thyA | 3074544 | c.-73T>G | upstream_gene_variant | 0.17 |
thyA | 3074645 | c.-174T>G | upstream_gene_variant | 0.14 |
ald | 3086659 | c.-161A>T | upstream_gene_variant | 0.23 |
ald | 3086987 | p.Gln56His | missense_variant | 0.15 |
fbiA | 3641186 | p.Asn215Ile | missense_variant | 0.17 |
embC | 4239793 | c.-70A>C | upstream_gene_variant | 0.24 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246893 | p.Asp127Ala | missense_variant | 0.16 |
embB | 4249287 | p.Gln925Arg | missense_variant | 0.12 |
ethA | 4327352 | p.Met41Thr | missense_variant | 0.14 |