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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.080 | 12 | 120979061 | missense variant | C/T | snv | 2.9E-02 | 2.2E-02 |
|
0.850 | 0.857 | 1 | 2004 | 2018 | |||||||
|
0.827 | 0.280 | 12 | 120997784 | synonymous variant | G/A;T | snv | 6.7E-06; 0.40 |
|
0.820 | 1.000 | 1 | 2009 | 2011 | ||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.800 | 1.000 | 7 | 2010 | 2019 | ||||||||
|
1.000 | 0.080 | 12 | 120983004 | intron variant | G/A | snv | 0.28 |
|
0.800 | 1.000 | 5 | 2009 | 2019 | ||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.800 | 1.000 | 4 | 2010 | 2018 | ||||||||
|
0.925 | 0.160 | 12 | 120987058 | intron variant | A/C;G;T | snv |
|
0.800 | 1.000 | 4 | 2008 | 2019 | |||||||||
|
0.925 | 0.160 | 12 | 120986153 | intron variant | C/T | snv | 0.62 |
|
0.800 | 1.000 | 3 | 2013 | 2019 | ||||||||
|
12 | 121001630 | 3 prime UTR variant | G/A | snv | 0.31 |
|
0.800 | 1.000 | 2 | 2008 | 2019 | ||||||||||
|
0.827 | 0.280 | 12 | 120997784 | synonymous variant | G/A;T | snv | 6.7E-06; 0.40 |
|
0.800 | 1.000 | 2 | 2012 | 2019 | ||||||||
|
12 | 120982457 | intron variant | A/C;G | snv |
|
0.800 | 1.000 | 2 | 2012 | 2019 | |||||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 12 | 120989098 | intron variant | G/A;C;T | snv |
|
0.800 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
0.882 | 0.160 | 12 | 120979185 | intron variant | A/G | snv | 0.29 |
|
0.800 | 1.000 | 1 | 2012 | 2017 | ||||||||
|
0.925 | 0.160 | 12 | 120987058 | intron variant | A/C;G;T | snv |
|
0.800 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.780 | 1.000 | 1 | 2006 | 2018 | ||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.730 | 1.000 | 2 | 2009 | 2018 | ||||||||
|
0.882 | 0.160 | 12 | 120979185 | intron variant | A/G | snv | 0.29 |
|
0.700 | 1.000 | 3 | 2017 | 2018 | ||||||||
|
0.882 | 0.160 | 12 | 120979185 | intron variant | A/G | snv | 0.29 |
|
0.700 | 1.000 | 2 | 2013 | 2019 | ||||||||
|
12 | 120982068 | intron variant | G/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
12 | 120982123 | intron variant | T/C | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.080 | 12 | 120981253 | intron variant | T/C | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.120 | 12 | 120990604 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |