Run ID: ERR970454
Sample name:
Date: 02-04-2023 12:02:17
Number of reads: 7993810
Percentage reads mapped: 98.65
Strain: lineage4.1.2
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 |
lineage4.1 | Euro-American | T;X;H | None | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.97 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6123 | p.Ala295Gly | missense_variant | 0.98 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 764944 | p.His525Gln | missense_variant | 0.97 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.98 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1417140 | p.Ala70Ser | missense_variant | 0.99 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673249 | c.-191C>T | upstream_gene_variant | 0.97 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101847 | p.Leu399Pro | missense_variant | 0.97 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
folC | 2747022 | p.Val193Ile | missense_variant | 0.99 |
thyA | 3073806 | c.666C>G | synonymous_variant | 0.24 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448894 | p.Tyr131Asp | missense_variant | 0.99 |
Rv3083 | 3449642 | p.Asn380Ser | missense_variant | 0.99 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.99 |
fbiA | 3641164 | p.Ile208Val | missense_variant | 0.97 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.99 |
aftB | 4268861 | c.-25T>C | upstream_gene_variant | 0.99 |
ubiA | 4269340 | p.Gly165Val | missense_variant | 0.93 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |