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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 5 | 112839693 | stop gained | C/T | snv | 0.700 | 1.000 | 7 | 1992 | 2015 | |||||||
|
1 | 5 | 112839879 | stop gained | C/A;T | snv | 0.700 | 1.000 | 7 | 1992 | 2014 | |||||||
|
1 | 5 | 112839729 | stop gained | G/T | snv | 0.700 | 1.000 | 5 | 1992 | 2015 | |||||||
|
1 | 5 | 112839726 | stop gained | C/T | snv | 0.700 | 1.000 | 5 | 1994 | 2014 | |||||||
|
1 | 5 | 112839510 | stop gained | G/A;T | snv | 0.700 | 1.000 | 4 | 1992 | 2015 | |||||||
|
1 | 5 | 112838674 | missense variant | A/G | snv | 0.700 | 0 | ||||||||||
|
42 | 0.649 | 0.440 | 5 | 112839514 | missense variant | T/A | snv | 8.0E-06; 2.0E-03 | 1.2E-03 | 0.030 | 1.000 | 3 | 1998 | 2005 | |||
|
36 | 0.658 | 0.440 | 5 | 112839511 | frameshift variant | TAAA/- | delins | 0.030 | 1.000 | 3 | 1998 | 2005 | |||||
|
17 | 0.732 | 0.200 | 5 | 112839543 | missense variant | G/C | snv | 4.4E-03 | 5.6E-03 | 0.010 | 1.000 | 1 | 1998 | 1998 | |||
|
10 | 0.776 | 0.080 | 5 | 112761654 | intron variant | A/G | snv | 9.6E-04 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
11 | 0.851 | 0.120 | 5 | 112838934 | stop gained | C/A;T | snv | 8.0E-06 | 0.700 | 1.000 | 5 | 1990 | 2014 | ||||
|
6 | 0.882 | 0.120 | 5 | 112838220 | stop gained | C/A;T | snv | 0.700 | 1.000 | 4 | 1992 | 2014 | |||||
|
5 | 0.925 | 0.120 | 5 | 112839942 | stop gained | C/G;T | snv | 4.0E-06 | 0.700 | 1.000 | 12 | 1992 | 2015 | ||||
|
3 | 0.925 | 0.120 | 5 | 112839606 | stop gained | C/G;T | snv | 0.700 | 1.000 | 8 | 1992 | 2015 | |||||
|
2 | 1.000 | 0.120 | 5 | 112839531 | missense variant | A/G | snv | 0.700 | 0 |