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 | 17 | 17798371 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 17 | 17797633 | missense variant | A/C;G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 17 | 17795909 | frameshift variant | AAGA/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Mental Disorders | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Mental Disorders | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Mental Disorders | 0.700 | 0 | |||||||||||
|
0.776 | 0.160 | 17 | 17795417 | frameshift variant | -/G | delins |
|
Behavior and Behavior Mechanisms | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 17 | 17797619 | frameshift variant | -/A | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 17 | 17795221 | stop gained | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.200 | 17 | 17795278 | frameshift variant | GGCAT/- | delins |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | 0.700 | 0 | |||||||||||
|
0.763 | 0.200 | 17 | 17811787 | splice region variant | G/A | snv | 0.45 | 0.33 |
|
Endocrine System Diseases | 0.010 | 1.000 | 1 | 2006 | 2006 |