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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.701 | 0.360 | 11 | 17388025 | stop gained | T/A;C | snv | 0.64 |
|
0.900 | 0.906 | 64 | 1998 | 2019 | ||||||||
|
0.827 | 0.160 | 11 | 17387083 | missense variant | C/T | snv | 0.64 | 0.71 |
|
0.860 | 0.941 | 17 | 2007 | 2018 | |||||||
|
0.807 | 0.200 | 11 | 17387595 | missense variant | C/A;T | snv |
|
0.810 | 1.000 | 14 | 2004 | 2017 | |||||||||
|
0.752 | 0.240 | 11 | 17387490 | missense variant | C/A;T | snv |
|
0.810 | 1.000 | 14 | 2004 | 2017 | |||||||||
|
0.827 | 0.160 | 11 | 17387937 | missense variant | T/C | snv |
|
0.810 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
0.790 | 0.240 | 11 | 17387943 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.810 | 1.000 | 13 | 2004 | 2017 | ||||||||
|
0.882 | 0.160 | 11 | 17387916 | missense variant | A/C | snv |
|
0.810 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
0.882 | 0.080 | 11 | 17387413 | missense variant | C/T | snv | 4.0E-06 |
|
0.810 | 1.000 | 2 | 2012 | 2017 | ||||||||
|
0.882 | 0.160 | 11 | 17387190 | missense variant | C/A;T | snv | 4.0E-06; 1.2E-05 |
|
0.800 | 1.000 | 17 | 1995 | 2013 | ||||||||
|
1.000 | 0.080 | 11 | 17387989 | missense variant | A/C;G | snv |
|
0.800 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
0.882 | 0.120 | 11 | 17387206 | missense variant | T/C;G | snv |
|
0.800 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
0.851 | 0.240 | 11 | 17387934 | missense variant | C/T | snv |
|
0.800 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
0.732 | 0.360 | 11 | 17387917 | missense variant | C/T | snv |
|
0.800 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
0.882 | 0.160 | 11 | 17387593 | missense variant | T/G | snv |
|
0.800 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
1.000 | 0.080 | 11 | 17387583 | missense variant | T/C | snv |
|
0.800 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
1.000 | 0.080 | 11 | 17387582 | missense variant | C/G | snv |
|
0.800 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
0.827 | 0.280 | 11 | 17387491 | missense variant | G/A | snv |
|
0.800 | 1.000 | 13 | 2004 | 2017 | |||||||||
|
1.000 | 0.120 | 11 | 17387331 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
0.800 | 1.000 | 12 | 1995 | 2009 | |||||||
|
1.000 | 0.120 | 11 | 17387316 | missense variant | T/C | snv | 4.4E-05 | 1.4E-05 |
|
0.800 | 1.000 | 12 | 1995 | 2009 | |||||||
|
1.000 | 0.120 | 11 | 17387626 | missense variant | C/T | snv |
|
0.800 | 1.000 | 12 | 1995 | 2009 | |||||||||
|
0.827 | 0.160 | 11 | 17387248 | missense variant | C/T | snv | 2.4E-05 | 2.8E-05 |
|
0.800 | 1.000 | 12 | 1995 | 2009 | |||||||
|
1.000 | 0.080 | 11 | 17390274 | upstream gene variant | C/T | snv | 0.72 |
|
0.800 | 1.000 | 2 | 2011 | 2019 | ||||||||
|
0.827 | 0.080 | 11 | 17387968 | missense variant | A/G | snv |
|
0.800 | 1.000 | 2 | 2005 | 2005 | |||||||||
|
0.925 | 0.080 | 11 | 17387935 | missense variant | C/G;T | snv |
|
0.800 | 1.000 | 2 | 2005 | 2005 | |||||||||
|
0.882 | 0.080 | 11 | 17387413 | missense variant | C/T | snv | 4.0E-06 |
|
0.720 | 1.000 | 2 | 2007 | 2012 |