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 | 0.080 | 5 | 62352594 | missense variant | G/C | snv | 7.0E-06 |
|
Nutritional and Metabolic Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
Eye Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.700 | 0 | |||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.790 | 0.160 | 5 | 62361307 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.882 | 0.120 | 5 | 62361319 | missense variant | G/A | snv |
|
0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
0.882 | 0.120 | 5 | 62361319 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.882 | 0.120 | 5 | 62361319 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 5 | 62361328 | missense variant | C/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 5 | 62361330 | missense variant | C/G;T | snv | 4.2E-06 |
|
0.800 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.040 | 5 | 62396136 | intron variant | C/A | snv | 0.28 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 5 | 62407706 | intron variant | G/A;T | snv | 0.41 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 |