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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 7 | 140781620 | missense variant | A/C | snv |
|
0.800 | 1.000 | 10 | 2006 | 2015 | |||||||||
|
1.000 | 0.160 | 7 | 140781609 | missense variant | A/C | snv |
|
0.800 | 1.000 | 4 | 2006 | 2009 | |||||||||
|
0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 |
|
0.900 | 0.975 | 10 | 2004 | 2020 | ||||||||
|
0.925 | 0.160 | 7 | 140777032 | missense variant | A/C;G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.280 | 7 | 140753350 | missense variant | A/C;T | snv |
|
0.800 | 1.000 | 4 | 2006 | 2012 | |||||||||
|
0.763 | 0.400 | 7 | 140753345 | missense variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2002 | 2002 | |||||||||
|
0.807 | 0.280 | 7 | 140749365 | missense variant | A/C;T | snv |
|
0.800 | 1.000 | 1 | 2006 | 2014 | |||||||||
|
0.851 | 0.280 | 7 | 140753350 | missense variant | A/C;T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.160 | 7 | 140781605 | missense variant | A/G | snv | 4.0E-06 |
|
0.800 | 1.000 | 4 | 2006 | 2009 | ||||||||
|
1.000 | 0.080 | 7 | 140781623 | missense variant | C/A | snv |
|
0.800 | 1.000 | 10 | 2006 | 2015 | |||||||||
|
0.925 | 0.200 | 7 | 140778053 | missense variant | C/A;G | snv |
|
0.800 | 1.000 | 1 | 2006 | 2014 | |||||||||
|
0.925 | 0.160 | 7 | 140777013 | missense variant | C/A;G | snv |
|
0.800 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
0.776 | 0.240 | 7 | 140781611 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.800 | 1.000 | 6 | 2002 | 2014 | ||||||||
|
0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv |
|
0.800 | 1.000 | 4 | 2002 | 2014 | |||||||||
|
0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.800 | 1.000 | 4 | 2006 | 2009 | ||||||||
|
0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.800 | 1.000 | 1 | 2003 | 2003 | ||||||||
|
0.742 | 0.320 | 7 | 140781603 | stop gained | C/A;G;T | snv |
|
0.800 | 1.000 | 1 | 2003 | 2003 | |||||||||
|
0.776 | 0.240 | 7 | 140781611 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.800 | 1.000 | 0 | 2013 | 2014 | ||||||||
|
0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.807 | 0.280 | 7 | 140753349 | missense variant | C/A;G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.400 | 7 | 140753348 | missense variant | C/A;T | snv |
|
0.800 | 1.000 | 4 | 2006 | 2009 | |||||||||
|
0.882 | 0.200 | 7 | 140801536 | missense variant | C/G | snv |
|
0.810 | 1.000 | 1 | 2006 | 2014 | |||||||||
|
1.000 | 0.120 | 7 | 140753379 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.240 | 7 | 140753339 | missense variant | G/A;C | snv |
|
0.800 | 1.000 | 5 | 2006 | 2014 |