Run ID: ERR2229165
Sample name:
Date: 31-03-2023 16:46:16
Number of reads: 227354
Percentage reads mapped: 98.89
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
mshA | 575904 | p.Ala186Glu | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 1.0 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.5 |
rpoB | 763083 | p.Arg1093Ser | missense_variant | 0.4 |
rpoB | 763305 | p.Ser1167Cys | missense_variant | 0.18 |
mmpL5 | 776958 | p.Gln508Leu | missense_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
embR | 1416265 | c.1083C>A | synonymous_variant | 0.13 |
embR | 1416622 | c.726C>T | synonymous_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833681 | p.Asp47Gly | missense_variant | 0.33 |
rpsA | 1834322 | p.Glu261* | stop_gained | 0.33 |
ndh | 2102796 | p.Gln83* | stop_gained | 0.5 |
PPE35 | 2167745 | p.Thr956Arg | missense_variant | 0.17 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.17 |
PPE35 | 2167965 | p.Ala883Gly | missense_variant | 0.45 |
PPE35 | 2167967 | c.2646A>C | synonymous_variant | 0.45 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.2 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.2 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.2 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.2 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.23 |
PPE35 | 2169910 | p.Asn235Tyr | missense_variant | 0.14 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.41 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.5 |
PPE35 | 2170779 | c.-167A>G | upstream_gene_variant | 0.12 |
Rv1979c | 2221969 | p.Ser399Phe | missense_variant | 0.2 |
Rv1979c | 2222416 | p.Arg250Leu | missense_variant | 0.5 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714327 | p.Gly336Ser | missense_variant | 0.33 |
Rv2752c | 3065143 | p.Gly350Val | missense_variant | 0.25 |
ald | 3087348 | p.Gly177Ser | missense_variant | 0.4 |
ald | 3087894 | c.1076delT | frameshift_variant | 0.67 |
alr | 3841546 | c.-126C>A | upstream_gene_variant | 0.23 |
ddn | 3987173 | c.330C>A | synonymous_variant | 0.2 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.25 |
clpC1 | 4038679 | p.Pro676Thr | missense_variant | 0.33 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.75 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.67 |
embA | 4243755 | p.Thr175Ala | missense_variant | 0.5 |
embA | 4244184 | p.Ser318Leu | missense_variant | 0.5 |
embA | 4244324 | c.1092T>C | synonymous_variant | 0.33 |
embA | 4245364 | p.Phe711Cys | missense_variant | 0.17 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.5 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.4 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.4 |
embB | 4246795 | c.282G>A | synonymous_variant | 1.0 |
aftB | 4267383 | p.Ala485Gly | missense_variant | 0.4 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |