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 | 0.120 | 3 | 33068891 | missense variant | G/A | snv | 1.8E-02 | 1.6E-02 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.882 | 0.120 | 3 | 33045708 | non coding transcript exon variant | A/C | snv | 0.19 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.120 | 3 | 33045708 | non coding transcript exon variant | A/C | snv | 0.19 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.882 | 0.120 | 3 | 33045708 | non coding transcript exon variant | A/C | snv | 0.19 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.925 | 0.160 | 3 | 33014263 | missense variant | C/A | snv |
|
0.010 | 1.000 | 1 | 1997 | 1997 | |||||||||
|
0.925 | 0.120 | 3 | 33016744 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.827 | 0.160 | 3 | 33014292 | missense variant | T/C | snv | 1.2E-05 |
|
0.010 | 1.000 | 1 | 2001 | 2001 | ||||||||
|
0.925 | 0.160 | 3 | 33021576 | missense variant | T/C;G | snv |
|
0.010 | 1.000 | 1 | 2001 | 2001 | |||||||||
|
0.807 | 0.160 | 3 | 33072637 | missense variant | A/G;T | snv |
|
0.010 | 1.000 | 1 | 2003 | 2003 | |||||||||
|
0.807 | 0.200 | 3 | 33072613 | missense variant | C/T | snv | 3.6E-05 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
1.000 | 0.120 | 3 | 33014196 | missense variant | T/A;C | snv | 4.7E-02 |
|
0.010 | 1.000 | 1 | 2000 | 2000 | ||||||||
|
0.807 | 0.160 | 3 | 33051956 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.807 | 0.160 | 3 | 33051956 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.807 | 0.160 | 3 | 33051956 | missense variant | G/A | snv | 8.0E-06 | 2.1E-05 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.080 | 3 | 33068890 | missense variant | C/G;T | snv | 4.0E-06; 8.0E-06 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.120 | 3 | 32997206 | missense variant | G/A;T | snv | 8.0E-06 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||
|
0.925 | 0.160 | 3 | 33051997 | missense variant | G/C | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
0.925 | 0.160 | 3 | 33051997 | missense variant | G/C | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2006 | 2006 | ||||||||
|
3 | 33058188 | missense variant | C/T | snv | 4.0E-06 |
|
0.010 | 1.000 | 1 | 2007 | 2007 | ||||||||||
|
1.000 | 0.120 | 3 | 33051980 | missense variant | A/G | snv | 5.6E-05 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||
|
0.925 | 0.120 | 3 | 33046194 | missense variant | C/T | snv | 2.1E-05 |
|
0.010 | 1.000 | 1 | 2000 | 2000 |