Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 0.925 | 0.080 | 2 | 166041354 | synonymous variant | A/G;T | snv | 0.73; 4.0E-06 | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||
|
1 | 1.000 | 0.080 | 2 | 166058626 | stop gained | G/C | snv | 0.700 | 0 | ||||||||
|
11 | 0.807 | 0.160 | 2 | 166036149 | frameshift variant | -/G | delins | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.080 | 2 | 166036051 | frameshift variant | TT/- | delins | 0.700 | 0 | ||||||||
|
8 | 0.776 | 0.240 | 2 | 166053034 | splice region variant | C/T | snv | 0.48 | 0.030 | 1.000 | 3 | 2010 | 2014 | ||||
|
3 | 0.882 | 0.080 | 2 | 166056450 | stop gained | A/G;T | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||
|
3 | 0.882 | 0.080 | 2 | 166041277 | missense variant | T/A;C | snv | 1.6E-05 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
1 | 1.000 | 0.080 | 2 | 165991477 | missense variant | C/A;T | snv | 2.0E-05; 8.0E-06 | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||
|
16 | 0.763 | 0.320 | 2 | 166242648 | missense variant | A/G | snv | 0.88 | 0.88 | 0.010 | 1.000 | 1 | 2020 | 2020 | |||
|
2 | 0.925 | 0.080 | 2 | 166122240 | intron variant | C/A | snv | 0.26 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
2 | 0.925 | 0.080 | 2 | 166288466 | missense variant | G/A | snv | 8.1E-06 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
2 | 0.925 | 0.080 | 2 | 166286614 | missense variant | C/T | snv | 9.4E-05 | 2.8E-05 | 0.010 | 1.000 | 1 | 2019 | 2019 |