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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.827 | 0.160 | 7 | 116777410 | missense variant | A/C;G | snv | 1.2E-05 |
|
0.700 | 1.000 | 7 | 1997 | 2015 | ||||||||
|
0.827 | 0.200 | 7 | 116783360 | missense variant | A/G | snv |
|
0.700 | 1.000 | 7 | 1997 | 2015 | |||||||||
|
0.882 | 0.120 | 7 | 116778827 | missense variant | T/C | snv |
|
0.700 | 1.000 | 7 | 1997 | 2015 | |||||||||
|
0.925 | 0.120 | 7 | 116782027 | missense variant | G/A;T | snv | 4.0E-06 |
|
0.700 | 1.000 | 7 | 1997 | 2015 | ||||||||
|
0.925 | 0.120 | 7 | 116783329 | missense variant | G/A | snv |
|
0.700 | 1.000 | 7 | 1997 | 2015 | |||||||||
|
0.925 | 0.120 | 7 | 116782048 | missense variant | C/G;T | snv |
|
0.700 | 1.000 | 7 | 1997 | 2015 | |||||||||
|
0.925 | 0.120 | 7 | 116777409 | missense variant | C/T | snv |
|
0.700 | 1.000 | 5 | 1997 | 1999 | |||||||||
|
0.925 | 0.120 | 7 | 116783420 | missense variant | T/C | snv |
|
0.700 | 1.000 | 5 | 1997 | 1999 | |||||||||
|
0.882 | 0.200 | 7 | 116783359 | missense variant | T/C | snv |
|
0.700 | 1.000 | 5 | 1997 | 1999 | |||||||||
|
0.925 | 0.120 | 7 | 116783329 | missense variant | G/A | snv |
|
0.700 | 1.000 | 5 | 1997 | 2013 | |||||||||
|
0.882 | 0.160 | 7 | 116783353 | missense variant | G/A;C | snv |
|
0.700 | 1.000 | 5 | 1997 | 1999 | |||||||||
|
0.882 | 0.120 | 7 | 116778827 | missense variant | T/C | snv |
|
0.700 | 1.000 | 4 | 1997 | 2001 | |||||||||
|
0.807 | 0.120 | 7 | 116783374 | missense variant | T/G | snv |
|
0.020 | 1.000 | 2 | 2005 | 2009 | |||||||||
|
0.807 | 0.120 | 7 | 116783374 | missense variant | T/G | snv |
|
0.710 | 1.000 | 2 | 2003 | 2007 | |||||||||
|
0.827 | 0.160 | 7 | 116777410 | missense variant | A/C;G | snv | 1.2E-05 |
|
0.700 | 1.000 | 2 | 2013 | 2014 | ||||||||
|
0.925 | 0.120 | 7 | 116777409 | missense variant | C/T | snv |
|
0.700 | 1.000 | 2 | 2008 | 2014 | |||||||||
|
0.925 | 0.120 | 7 | 116783420 | missense variant | T/C | snv |
|
0.700 | 1.000 | 2 | 2013 | 2014 | |||||||||
|
0.827 | 0.200 | 7 | 116783360 | missense variant | A/G | snv |
|
0.710 | 1.000 | 2 | 2007 | 2017 | |||||||||
|
0.827 | 0.200 | 7 | 116783360 | missense variant | A/G | snv |
|
0.700 | 1.000 | 2 | 2002 | 2014 | |||||||||
|
0.827 | 0.200 | 7 | 116783360 | missense variant | A/G | snv |
|
0.020 | 1.000 | 2 | 2000 | 2002 | |||||||||
|
7 | 116717990 | intron variant | A/G;T | snv |
|
0.800 | 1.000 | 2 | 2013 | 2017 | |||||||||||
|
0.925 | 0.080 | 7 | 116699588 | missense variant | G/A;T | snv | 3.7E-03 |
|
0.020 | 1.000 | 2 | 2003 | 2005 | ||||||||
|
0.807 | 0.120 | 7 | 116783374 | missense variant | T/G | snv |
|
0.700 | 1.000 | 1 | 2002 | 2002 | |||||||||
|
0.807 | 0.120 | 7 | 116783374 | missense variant | T/G | snv |
|
0.010 | 1.000 | 1 | 2003 | 2003 | |||||||||
|
0.807 | 0.120 | 7 | 116783374 | missense variant | T/G | snv |
|
0.010 | 1.000 | 1 | 2003 | 2003 |