Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.800 | 1.000 | 1 | 2011 | 2012 | ||||||||||
|
2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | |||||||||
|
2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | |||||||||
|
0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||
|
0.851 | 0.240 | 2 | 21002409 | missense variant | C/T | snv | 0.70 | 0.78 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||
|
2 | 21018633 | intron variant | A/G | snv | 0.14 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
1.000 | 0.080 | 2 | 21003688 | intron variant | A/G | snv | 0.76 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
2 | 21011100 | missense variant | T/C | snv | 3.1E-02 | 2.9E-02 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
2 | 21011100 | missense variant | T/C | snv | 3.1E-02 | 2.9E-02 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
2 | 21011100 | missense variant | T/C | snv | 3.1E-02 | 2.9E-02 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
2 | 21011100 | missense variant | T/C | snv | 3.1E-02 | 2.9E-02 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 1 | 2012 | 2018 | |||||||||
|
0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2012 | 2018 | ||||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||
|
0.708 | 0.440 | 2 | 21009323 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.710 | 1.000 | 1 | 2011 | 2016 | |||||||
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |