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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.763 | 0.280 | 2 | 39022773 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.700 | 1.000 | 19 | 2007 | 2018 | ||||||||
|
0.851 | 0.160 | 12 | 112489048 | missense variant | C/A;T | snv |
|
0.700 | 1.000 | 13 | 2004 | 2014 | |||||||||
|
0.807 | 0.320 | 12 | 112489080 | missense variant | T/A;G | snv |
|
0.700 | 1.000 | 12 | 2002 | 2013 | |||||||||
|
0.742 | 0.240 | 12 | 112489104 | missense variant | C/A;G | snv |
|
0.700 | 1.000 | 10 | 2005 | 2012 | |||||||||
|
0.667 | 0.480 | 3 | 12604200 | missense variant | G/A;C | snv | 4.0E-06 |
|
0.700 | 1.000 | 10 | 1992 | 2018 | ||||||||
|
0.827 | 0.160 | 12 | 112450497 | missense variant | A/C | snv |
|
0.700 | 1.000 | 9 | 2002 | 2011 | |||||||||
|
0.851 | 0.160 | 12 | 112473031 | missense variant | A/G | snv | 7.0E-06 |
|
0.700 | 1.000 | 9 | 2001 | 2011 | ||||||||
|
0.752 | 0.240 | 2 | 39022774 | missense variant | T/A;C | snv | 4.0E-06 |
|
0.700 | 1.000 | 8 | 2007 | 2014 | ||||||||
|
0.925 | 0.160 | 12 | 25245372 | missense variant | T/C | snv |
|
0.700 | 1.000 | 8 | 2007 | 2014 | |||||||||
|
0.776 | 0.280 | 12 | 112450361 | missense variant | G/A;C;T | snv |
|
0.700 | 1.000 | 7 | 2002 | 2014 | |||||||||
|
1.000 | 0.160 | 12 | 112489081 | missense variant | C/T | snv |
|
0.700 | 1.000 | 7 | 2004 | 2008 | |||||||||
|
0.752 | 0.280 | 12 | 112489086 | missense variant | A/G | snv | 4.0E-06 |
|
0.700 | 1.000 | 7 | 2002 | 2008 | ||||||||
|
0.882 | 0.200 | 2 | 39007168 | missense variant | C/T | snv |
|
0.700 | 1.000 | 7 | 2007 | 2013 | |||||||||
|
0.925 | 0.160 | 2 | 39058696 | missense variant | C/T | snv |
|
0.700 | 1.000 | 7 | 2007 | 2014 | |||||||||
|
0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv |
|
0.700 | 1.000 | 7 | 2013 | 2016 | |||||||||
|
0.827 | 0.160 | 3 | 12604189 | missense variant | G/A;C;T | snv |
|
0.700 | 1.000 | 6 | 2007 | 2013 | |||||||||
|
1.000 | 0.160 | 3 | 12604195 | missense variant | A/C;G;T | snv |
|
0.700 | 1.000 | 6 | 2003 | 2014 | |||||||||
|
0.882 | 0.160 | 12 | 112472954 | missense variant | A/G | snv |
|
0.700 | 1.000 | 6 | 2003 | 2014 | |||||||||
|
0.925 | 0.160 | 11 | 119278165 | splice acceptor variant | G/C;T | snv |
|
0.700 | 1.000 | 6 | 2009 | 2015 | |||||||||
|
0.882 | 0.200 | 2 | 39023131 | missense variant | C/T | snv | 4.0E-06 |
|
0.700 | 1.000 | 6 | 2007 | 2010 | ||||||||
|
0.925 | 0.160 | 12 | 112450386 | missense variant | A/T | snv |
|
0.700 | 1.000 | 6 | 2004 | 2017 | |||||||||
|
0.683 | 0.440 | 1 | 114716127 | missense variant | C/A;G;T | snv |
|
0.700 | 1.000 | 5 | 2000 | 2010 | |||||||||
|
0.882 | 0.160 | 12 | 112488454 | missense variant | G/C | snv |
|
0.700 | 1.000 | 5 | 2006 | 2009 | |||||||||
|
0.851 | 0.200 | 2 | 39051211 | missense variant | G/T | snv |
|
0.700 | 1.000 | 5 | 2007 | 2010 | |||||||||
|
0.882 | 0.200 | 7 | 140801536 | missense variant | C/G | snv |
|
0.700 | 1.000 | 5 | 2006 | 2011 |