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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.120 | 4 | 88038371 | missense variant | C/T | snv |
|
0.700 | 1.000 | 9 | 2002 | 2017 | |||||||||
|
1.000 | 0.120 | 4 | 88038365 | stop gained | C/T | snv | 4.0E-06 | 1.4E-05 |
|
0.700 | 1.000 | 7 | 1999 | 2016 | |||||||
|
0.925 | 0.120 | 4 | 88043458 | splice donor variant | G/A | snv | 8.0E-06 | 1.4E-05 |
|
0.700 | 1.000 | 5 | 2000 | 2012 | |||||||
|
0.925 | 0.120 | 4 | 88065479 | stop gained | C/T | snv | 7.0E-06 |
|
0.700 | 1.000 | 4 | 1996 | 2013 | ||||||||
|
1.000 | 0.120 | 4 | 88007931 | frameshift variant | C/-;CC | delins |
|
0.700 | 1.000 | 3 | 1999 | 2012 | |||||||||
|
0.925 | 0.120 | 4 | 88019499 | stop gained | C/T | snv | 7.0E-06 |
|
0.700 | 1.000 | 3 | 2012 | 2016 | ||||||||
|
1.000 | 0.120 | 4 | 88058104 | splice donor variant | G/A | snv |
|
0.700 | 1.000 | 2 | 2007 | 2012 | |||||||||
|
0.925 | 0.120 | 4 | 88038380 | stop gained | C/T | snv | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.120 | 4 | 88008244 | frameshift variant | G/- | delins | 7.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.120 | 4 | 88046647 | stop gained | T/A;C | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.120 | 4 | 88052018 | frameshift variant | TA/- | delins |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.120 | 4 | 88056143 | stop gained | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.120 | 16 | 2106172 | frameshift variant | G/- | delins |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.120 | 4 | 88008174 | frameshift variant | G/- | delins |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.120 | 11 | 62646584 | inframe deletion | TACCGC/- | delins | 7.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 |
|
0.060 | 1.000 | 6 | 2002 | 2014 | ||||||||
|
0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 |
|
0.030 | 1.000 | 3 | 1997 | 2003 | |||||||
|
0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 |
|
0.020 | 1.000 | 2 | 1997 | 2000 | ||||||||
|
0.683 | 0.400 | 4 | 2904980 | missense variant | G/A;T | snv | 1.2E-05; 0.20 |
|
0.020 | 1.000 | 2 | 2003 | 2003 | ||||||||
|
1.000 | 0.120 | 1 | 230711810 | intron variant | C/A | snv | 0.19 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.925 | 0.120 | 4 | 88046854 | missense variant | A/T | snv |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.574 | 0.720 | 6 | 43770966 | missense variant | G/A | snv |
|
0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
0.925 | 0.240 | 9 | 95485696 | stop gained | G/C | snv |
|
0.010 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.120 | 4 | 88007759 | missense variant | C/T | snv |
|
0.010 | < 0.001 | 1 | 2003 | 2003 | |||||||||
|
1.000 | 0.120 | 1 | 204159726 | intron variant | T/C;G | snv |
|
0.010 | 1.000 | 1 | 2016 | 2016 |