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 | 16 | 57659478 | missense variant | A/G | snv |
|
0.700 | 1.000 | 10 | 2003 | 2015 | ||||||||||
|
1.000 | 16 | 57659478 | missense variant | A/G | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 1.000 | 10 | 2003 | 2015 | |||||||||
|
1.000 | 16 | 57659478 | missense variant | A/G | snv |
|
Nervous System Diseases | 0.700 | 1.000 | 10 | 2003 | 2015 | |||||||||
|
1.000 | 0.080 | 16 | 57656244 | missense variant | T/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.800 | 1.000 | 6 | 2004 | 2014 | ||||||||
|
1.000 | 0.080 | 16 | 57651407 | missense variant | G/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.800 | 1.000 | 6 | 2004 | 2014 | ||||||||
|
1.000 | 0.080 | 16 | 57651398 | missense variant | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.800 | 1.000 | 6 | 2004 | 2014 | ||||||||
|
1.000 | 0.080 | 16 | 57619621 | intron variant | T/G | snv | 8.4E-02 |
|
Neoplasms; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 16 | 57620664 | intron variant | C/T | snv | 3.4E-02 |
|
Neoplasms; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.080 | 16 | 57650297 | stop gained | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 1.000 | 1 | 2004 | 2004 | ||||||||
|
1.000 | 0.080 | 16 | 57661939 | missense variant | T/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.882 | 0.120 | 16 | 57655528 | stop gained | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 16 | 57655528 | stop gained | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 16 | 57655528 | stop gained | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 16 | 57655528 | stop gained | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 16 | 57655528 | stop gained | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.240 | 16 | 57660794 | frameshift variant | -/T | delins |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | 0.700 | 0 | |||||||||||
|
0.807 | 0.240 | 16 | 57660794 | frameshift variant | -/T | delins |
|
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.807 | 0.240 | 16 | 57660794 | frameshift variant | -/T | delins |
|
Eye Diseases; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.807 | 0.240 | 16 | 57660794 | frameshift variant | -/T | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.807 | 0.240 | 16 | 57660794 | frameshift variant | -/T | delins |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.240 | 16 | 57660794 | frameshift variant | -/T | delins |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.807 | 0.240 | 16 | 57660794 | frameshift variant | -/T | delins |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | 16 | 57656620 | splice region variant | G/A;C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 16 | 57653985 | splice acceptor variant | G/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases | 0.700 | 0 | |||||||||||
|
0.851 | 0.080 | 16 | 57654103 | frameshift variant | CAGGACC/- | delins |
|
Behavior and Behavior Mechanisms | 0.700 | 0 |