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 | 0.320 | 1 | 156136984 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 |
|
0.830 | 1.000 | 0 | 2014 | 2018 | |||||||
|
0.851 | 0.200 | 1 | 156137203 | missense variant | C/T | snv | 1.4E-05 | 1.4E-05 |
|
0.820 | 1.000 | 10 | 2003 | 2013 | |||||||
|
0.827 | 0.200 | 1 | 156130693 | missense variant | G/A | snv |
|
0.820 | 1.000 | 0 | 2003 | 2017 | |||||||||
|
0.827 | 0.200 | 1 | 156137666 | missense variant | C/A;G;T | snv |
|
0.810 | 1.000 | 20 | 1999 | 2017 | |||||||||
|
0.925 | 0.120 | 1 | 156136952 | missense variant | G/A;C | snv | 1.4E-05 |
|
0.810 | 1.000 | 17 | 1999 | 2014 | ||||||||
|
0.882 | 0.160 | 1 | 156130741 | missense variant | G/A | snv |
|
0.810 | 1.000 | 17 | 1999 | 2012 | |||||||||
|
0.776 | 0.200 | 1 | 156137204 | missense variant | G/A;C | snv | 4.1E-05 |
|
0.810 | 1.000 | 3 | 2002 | 2006 | ||||||||
|
0.776 | 0.200 | 1 | 156136413 | missense variant | C/T | snv |
|
0.810 | 1.000 | 2 | 2008 | 2017 | |||||||||
|
1.000 | 0.120 | 1 | 156137210 | missense variant | C/T | snv |
|
0.810 | 1.000 | 0 | 2005 | 2005 | |||||||||
|
0.776 | 0.200 | 1 | 156138507 | missense variant | C/T | snv | 1.5E-04 | 1.0E-04 |
|
0.810 | 1.000 | 0 | 2006 | 2006 | |||||||
|
0.925 | 0.120 | 1 | 156130757 | missense variant | G/A;C | snv | 4.8E-05 |
|
0.800 | 1.000 | 20 | 1999 | 2017 | ||||||||
|
0.925 | 0.160 | 1 | 156115172 | missense variant | T/A;G | snv |
|
0.800 | 1.000 | 20 | 1999 | 2017 | |||||||||
|
0.882 | 0.160 | 1 | 156134474 | missense variant | C/A;G | snv |
|
0.800 | 1.000 | 20 | 1999 | 2017 | |||||||||
|
1.000 | 0.040 | 1 | 156134497 | missense variant | A/G;T | snv |
|
0.800 | 1.000 | 17 | 1999 | 2012 | |||||||||
|
0.653 | 0.480 | 1 | 156136985 | missense variant | G/A;T | snv |
|
0.800 | 1.000 | 11 | 2000 | 2014 | |||||||||
|
0.776 | 0.200 | 1 | 156137204 | missense variant | G/A;C | snv | 4.1E-05 |
|
0.800 | 1.000 | 11 | 2000 | 2014 | ||||||||
|
0.925 | 0.080 | 1 | 156138534 | missense variant | G/A;T | snv | 8.2E-06 | 7.0E-06 |
|
0.800 | 1.000 | 11 | 2000 | 2014 | |||||||
|
0.925 | 0.080 | 1 | 156136934 | missense variant | G/A | snv |
|
0.800 | 1.000 | 11 | 2000 | 2014 | |||||||||
|
0.925 | 0.320 | 1 | 156115094 | missense variant | T/G | snv |
|
0.800 | 1.000 | 3 | 2003 | 2009 | |||||||||
|
0.882 | 0.120 | 1 | 156134910 | missense variant | C/G;T | snv |
|
0.800 | 1.000 | 2 | 2008 | 2017 | |||||||||
|
0.851 | 0.120 | 1 | 156134839 | missense variant | G/A | snv |
|
0.800 | 1.000 | 2 | 2012 | 2017 | |||||||||
|
0.925 | 0.120 | 1 | 156134860 | missense variant | G/A | snv |
|
0.800 | 1.000 | 2 | 2000 | 2017 | |||||||||
|
0.776 | 0.200 | 1 | 156137204 | missense variant | G/A;C | snv | 4.1E-05 |
|
0.800 | 1.000 | 2 | 2012 | 2017 | ||||||||
|
0.882 | 0.160 | 1 | 156137213 | missense variant | T/C | snv |
|
0.800 | 1.000 | 2 | 2012 | 2017 | |||||||||
|
1.000 | 0.120 | 1 | 156136103 | missense variant | T/C | snv |
|
0.800 | 1.000 | 1 | 2008 | 2008 |