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 | 3 | 49098261 | splice region variant | G/A;T | snv | 3.2E-05 | 3.5E-05 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Eye Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Mental Disorders | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Nervous System Diseases; Mental Disorders | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49099606 | missense variant | T/C | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 3 | 49102251 | frameshift variant | C/- | delins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 3 | 49099346 | frameshift variant | G/- | delins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 3 | 49099176 | frameshift variant | GT/- | delins |
|
0.700 | 0 | |||||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Mental Disorders | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Eye Diseases; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Nervous System Diseases; Mental Disorders | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 3 | 49100222 | missense variant | G/A;C;T | snv | 8.0E-05; 4.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 |