Run ID: ERR8774136
Sample name:
Date: 02-04-2023 08:24:07
Number of reads: 745197
Percentage reads mapped: 99.64
Strain: lineage4.8
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7329 | p.Asp10Tyr | missense_variant | 0.12 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9184 | p.Arg628Leu | missense_variant | 1.0 |
fgd1 | 491226 | c.444C>T | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777864 | p.Val206Glu | missense_variant | 0.15 |
mmpS5 | 778828 | p.Gln26His | missense_variant | 0.33 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781492 | c.-68G>A | upstream_gene_variant | 0.12 |
Rv1258c | 1406520 | p.Gly274Val | missense_variant | 0.12 |
Rv1258c | 1406854 | c.487T>C | synonymous_variant | 0.12 |
embR | 1416272 | p.Ser359Tyr | missense_variant | 0.4 |
embR | 1416534 | c.813delC | frameshift_variant | 0.22 |
atpE | 1461158 | c.114T>C | synonymous_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471674 | n.-172G>T | upstream_gene_variant | 0.5 |
rrl | 1475308 | n.1651C>A | non_coding_transcript_exon_variant | 0.33 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101863 | p.Leu394Met | missense_variant | 0.12 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.2 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2519207 | p.Gly365Cys | missense_variant | 0.12 |
eis | 2715469 | c.-137T>C | upstream_gene_variant | 0.11 |
eis | 2715473 | c.-141A>G | upstream_gene_variant | 0.11 |
Rv3083 | 3448497 | c.-7T>A | upstream_gene_variant | 1.0 |
fbiA | 3640808 | c.266_267insAGC | disruptive_inframe_insertion | 0.12 |
fbiA | 3640812 | p.Gln90His | missense_variant | 0.13 |
fbiA | 3640813 | p.Glu91Gln | missense_variant | 0.13 |
fbiA | 3640816 | p.Leu92Phe | missense_variant | 0.13 |
fbiA | 3640819 | p.Val93Leu | missense_variant | 0.13 |
fbiA | 3640822 | c.281_283delGCT | disruptive_inframe_deletion | 0.13 |
alr | 3840764 | c.657G>C | synonymous_variant | 1.0 |
rpoA | 3878039 | p.Ala157Ser | missense_variant | 0.13 |
panD | 4043885 | p.Asp133His | missense_variant | 0.11 |
panD | 4044170 | p.Leu38Met | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4248476 | p.Pro655Thr | missense_variant | 0.14 |
aftB | 4268863 | c.-27G>A | upstream_gene_variant | 0.15 |
ubiA | 4269082 | p.Ser251Trp | missense_variant | 0.11 |
ethR | 4327743 | p.Phe65Leu | missense_variant | 0.13 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |