Run ID: ERR2229160
Sample name:
Date: 31-03-2023 16:45:40
Number of reads: 236060
Percentage reads mapped: 99.21
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.64 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
ccsA | 620475 | c.585G>T | synonymous_variant | 0.4 |
rpoB | 760658 | p.Glu284Asp | missense_variant | 0.33 |
rpoB | 763183 | p.Cys1126Phe | missense_variant | 0.4 |
rpoC | 767268 | p.Ala1300Asp | missense_variant | 0.4 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303160 | p.Gly77Glu | missense_variant | 0.5 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1305190 | p.Ala754Thr | missense_variant | 0.4 |
embR | 1416622 | p.Asp242Glu | missense_variant | 0.67 |
embR | 1417450 | c.-103C>T | upstream_gene_variant | 0.22 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471839 | n.-7G>A | upstream_gene_variant | 0.67 |
ndh | 2102074 | p.Met323Lys | missense_variant | 1.0 |
ndh | 2102561 | c.481delT | frameshift_variant | 0.22 |
PPE35 | 2168123 | c.2490A>T | synonymous_variant | 0.67 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169168 | p.Leu482Ser | missense_variant | 0.29 |
PPE35 | 2169394 | p.Ala407Thr | missense_variant | 0.15 |
PPE35 | 2169397 | p.Gly406Ser | missense_variant | 0.16 |
PPE35 | 2169866 | c.747G>A | synonymous_variant | 0.15 |
PPE35 | 2169879 | p.Phe245Ser | missense_variant | 0.17 |
PPE35 | 2169882 | p.Ser244Asn | missense_variant | 0.18 |
PPE35 | 2169890 | c.723C>T | synonymous_variant | 0.22 |
PPE35 | 2169893 | c.720C>A | synonymous_variant | 0.22 |
PPE35 | 2169902 | p.Leu237Phe | missense_variant | 0.2 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.27 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.3 |
PPE35 | 2170147 | p.Ser156Ala | missense_variant | 0.12 |
PPE35 | 2170372 | p.Thr81Ala | missense_variant | 0.18 |
PPE35 | 2170376 | c.237G>A | synonymous_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288765 | c.477G>T | synonymous_variant | 0.13 |
pncA | 2288837 | c.405C>T | synonymous_variant | 0.13 |
pncA | 2289209 | c.33C>T | synonymous_variant | 0.29 |
eis | 2714783 | p.Gln184* | stop_gained | 0.4 |
thyX | 3067911 | p.Ile12Thr | missense_variant | 0.25 |
thyA | 3074640 | c.-169G>A | upstream_gene_variant | 0.5 |
ald | 3086725 | c.-95A>G | upstream_gene_variant | 0.4 |
Rv3236c | 3612357 | p.Glu254* | stop_gained | 0.33 |
clpC1 | 4040562 | p.Ser48* | stop_gained | 0.2 |
clpC1 | 4040605 | p.Leu34Ile | missense_variant | 0.22 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.5 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.75 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.75 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.75 |
embB | 4248221 | p.Pro570Ser | missense_variant | 0.2 |
aftB | 4267782 | p.Val352Gly | missense_variant | 0.25 |
ethR | 4326757 | c.-792C>G | upstream_gene_variant | 0.29 |
ethA | 4328055 | c.-582A>G | upstream_gene_variant | 0.33 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |