Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 0.882 | 0.120 | 2 | 47073816 | stop gained | C/T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
73 | 0.641 | 0.560 | 17 | 75494905 | frameshift variant | -/A | delins | 4.0E-06 | 0.700 | 0 | |||||||
|
73 | 0.641 | 0.560 | 17 | 75489265 | splice acceptor variant | G/C | snv | 0.700 | 0 | ||||||||
|
19 | 0.708 | 0.280 | 6 | 133893387 | 3 prime UTR variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
|
1 | 12 | 114361761 | intron variant | C/A | snv | 1.2E-03 | 0.010 | 1.000 | 1 | 2009 | 2009 | ||||||
|
3 | 1.000 | 0.080 | 12 | 114355868 | stop gained | G/C | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
4 | 0.925 | 0.120 | 12 | 114398639 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 6 | 84765153 | upstream gene variant | G/A;T | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
24 | 0.790 | 0.320 | 11 | 4091328 | missense variant | C/G;T | snv | 4.4E-05 | 0.700 | 0 | |||||||
|
11 | 0.882 | 0.080 | 6 | 21594732 | missense variant | C/A;T | snv | 4.6E-06 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
11 | 0.807 | 0.200 | 2 | 39051202 | missense variant | A/C;G | snv | 0.700 | 1.000 | 5 | 2007 | 2011 | |||||
|
3 | 0.925 | 0.120 | 15 | 67146869 | intron variant | T/G | snv | 0.43 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
8 | 0.807 | 0.280 | 22 | 19176222 | missense variant | G/A;C | snv | 2.0E-05 | 0.700 | 0 | |||||||
|
23 | 0.752 | 0.280 | 17 | 63957514 | missense variant | C/T | snv | 8.2E-06 | 1.4E-05 | 0.700 | 1.000 | 2 | 2004 | 2008 | |||
|
17 | 0.851 | 0.240 | 17 | 63947062 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 20 | 51790094 | missense variant | T/A | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
1 | 20 | 51791897 | missense variant | G/A | snv | 2.8E-05 | 2.1E-05 | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
|
14 | 0.790 | 0.160 | X | 20193547 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
16 | 0.776 | 0.360 | 1 | 155904470 | stop lost | C/A;G;T | snv | 0.700 | 0 | ||||||||
|
37 | 0.667 | 0.480 | 3 | 12604200 | missense variant | G/A;C | snv | 4.0E-06 | 0.700 | 1.000 | 2 | 2007 | 2007 | ||||
|
7 | 0.851 | 0.160 | 8 | 143818077 | splice acceptor variant | T/C;G | snv | 0.700 | 0 | ||||||||
|
14 | 0.752 | 0.280 | 12 | 112450416 | missense variant | A/G | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||
|
31 | 0.695 | 0.440 | 12 | 112477720 | missense variant | A/C;G | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.040 | 14 | 73211255 | intron variant | T/C;G | snv | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||
|
2 | 1.000 | 0.040 | 14 | 73136992 | 5 prime UTR variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2011 | 2011 |