Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 7 | 66994286 | stop gained | TA/AG | mnv |
|
0.710 | 1.000 | 15 | 2003 | 2018 | ||||||||||
|
1.000 | 7 | 66993416 | stop gained | A/C | snv |
|
0.700 | 1.000 | 4 | 2003 | 2014 | ||||||||||
|
0.925 | 7 | 66994286 | stop gained | T/A | snv | 1.7E-04 | 1.0E-03 |
|
0.010 | 1.000 | 1 | 2005 | 2005 | ||||||||
|
1.000 | 7 | 66988472 | stop gained | G/A | snv | 8.0E-06 |
|
0.700 | 0 | ||||||||||||
|
0.925 | 7 | 66994286 | stop gained | T/A | snv | 1.7E-04 | 1.0E-03 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | ||||||||||
|
0.925 | 7 | 66994286 | stop gained | T/A | snv | 1.7E-04 | 1.0E-03 |
|
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.925 | 7 | 66994286 | stop gained | T/A | snv | 1.7E-04 | 1.0E-03 |
|
0.700 | 0 | |||||||||||
|
0.925 | 7 | 66994286 | stop gained | T/A | snv | 1.7E-04 | 1.0E-03 |
|
0.700 | 0 | |||||||||||
|
0.925 | 7 | 66994286 | stop gained | T/A | snv | 1.7E-04 | 1.0E-03 |
|
0.700 | 0 | |||||||||||
|
0.925 | 7 | 66994286 | stop gained | T/A | snv | 1.7E-04 | 1.0E-03 |
|
0.700 | 0 | |||||||||||
|
1.000 | 7 | 66994271 | missense variant | T/C | snv |
|
0.700 | 1.000 | 4 | 2003 | 2014 | ||||||||||
|
1.000 | 7 | 66994339 | missense variant | T/C | snv |
|
0.700 | 1.000 | 4 | 2003 | 2014 | ||||||||||
|
1.000 | 7 | 66995394 | missense variant | G/T | snv | 8.0E-06 |
|
0.700 | 1.000 | 4 | 2003 | 2014 | |||||||||
|
0.925 | 7 | 66995320 | missense variant | T/C;G | snv | 6.0E-05 |
|
0.800 | 1.000 | 4 | 2003 | 2014 | |||||||||
|
0.925 | 7 | 66993299 | missense variant | C/G | snv | 7.0E-06 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 7 | 66991256 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 7 | 66993248 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.925 | 7 | 66993299 | missense variant | C/G | snv | 7.0E-06 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 7 | 66993288 | missense variant | C/A;T | snv | 1.2E-05; 9.1E-05 |
|
0.700 | 0 | ||||||||||||
|
0.925 | 7 | 66995320 | missense variant | T/C;G | snv | 6.0E-05 |
|
0.700 | 0 | ||||||||||||
|
0.925 | 7 | 66995320 | missense variant | T/C;G | snv | 6.0E-05 |
|
0.700 | 0 | ||||||||||||
|
0.925 | 7 | 66995320 | missense variant | T/C;G | snv | 6.0E-05 |
|
Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases | 0.700 | 0 | |||||||||||
|
0.851 | 0.040 | 7 | 66994210 | splice donor variant | A/C;G | snv | 4.0E-06; 3.9E-03 |
|
0.700 | 1.000 | 10 | 2003 | 2015 | ||||||||
|
0.882 | 0.040 | 7 | 66994211 | splice donor variant | C/G | snv | 4.0E-06 | 2.1E-05 |
|
0.700 | 1.000 | 5 | 2003 | 2014 | |||||||
|
0.851 | 0.040 | 7 | 66994210 | splice donor variant | A/C;G | snv | 4.0E-06; 3.9E-03 |
|
0.700 | 1.000 | 4 | 2003 | 2013 |