Run ID: ERR8774141
Sample name:
Date: 02-04-2023 08:24:12
Number of reads: 747187
Percentage reads mapped: 99.59
Strain: lineage4.4.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.4 | Euro-American | S;T | None | 1.0 |
lineage4.4.1 | Euro-American (S-type) | S;T | None | 1.0 |
lineage4.4.1.1 | Euro-American | S;Orphans | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5511 | p.Ser91Tyr | missense_variant | 0.29 |
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 | 765738 | p.Arg790Leu | missense_variant | 0.14 |
rpoC | 767156 | p.Gly1263Ser | missense_variant | 0.13 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776353 | p.Ser710Thr | missense_variant | 0.13 |
mmpL5 | 777497 | c.984A>G | synonymous_variant | 1.0 |
mmpR5 | 779339 | p.Leu117Arg | missense_variant | 0.18 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
embR | 1416570 | c.777delG | frameshift_variant | 0.11 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472717 | n.872C>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473361 | n.1516G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474282 | n.625G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475803 | n.2148delG | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476630 | n.2973A>C | non_coding_transcript_exon_variant | 0.2 |
rpsA | 1833763 | c.222C>T | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102990 | p.Val18Ala | missense_variant | 1.0 |
katG | 2155140 | c.972C>A | synonymous_variant | 0.13 |
PPE35 | 2169840 | p.Gly258Asp | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.17 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518223 | c.109T>C | synonymous_variant | 1.0 |
folC | 2747580 | p.Gly7Cys | missense_variant | 0.15 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3448608 | c.105G>A | synonymous_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612665 | p.Val151Ala | missense_variant | 1.0 |
clpC1 | 4039303 | p.Trp468Arg | missense_variant | 0.18 |
embC | 4241684 | p.Val608Leu | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246697 | p.Gly62Trp | missense_variant | 0.2 |
embB | 4246730 | p.Ser73Ala | missense_variant | 0.17 |
ethA | 4326187 | c.1287G>A | synonymous_variant | 0.13 |
ethR | 4327853 | p.Met102Thr | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |