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 | 1 | 8358216 | protein altering variant | -/AGGTGG | delins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 1 | 8358216 | missense variant | T/C | snv |
|
0.700 | 0 | |||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases | 0.700 | 0 | |||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms | 0.700 | 0 | |||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases | 0.700 | 0 | |||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
Behavior and Behavior Mechanisms | 0.700 | 0 | |||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications | 0.700 | 0 | |||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.280 | 1 | 8358231 | missense variant | T/A;C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 1 | 8656049 | frameshift variant | -/T | delins |
|
0.700 | 0 | |||||||||||||
|
1.000 | 1 | 8358232 | missense variant | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 1 | 8358235 | missense variant | A/G | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 1 | 8365848 | missense variant | C/T | snv | 1.6E-05 | 7.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 1 | 8358242 | missense variant | G/T | snv |
|
0.700 | 0 |