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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.851 | 0.080 | 7 | 129210500 | missense variant | G/T | snv |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
0.851 | 0.080 | 7 | 129210500 | missense variant | G/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.040 | 7 | 129210997 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 |
|
0.700 | 0 | ||||||||||
|
0.925 | 0.040 | 7 | 129210997 | missense variant | G/A | snv | 4.0E-05 | 2.8E-05 |
|
Neoplasms | 0.700 | 0 | |||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.700 | 0 | |||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Skin and Connective Tissue Diseases | 0.700 | 0 | |||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Skin and Connective Tissue Diseases | 0.700 | 0 | |||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases | 0.700 | 0 | |||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Skin and Connective Tissue Diseases | 0.700 | 0 | |||||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Skin and Connective Tissue Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.040 | 7 | 129209348 | missense variant | G/A;C | snv | 2.4E-05 |
|
Neoplasms | 0.700 | 1.000 | 3 | 2009 | 2015 | |||||||
|
0.925 | 0.040 | 7 | 129209348 | missense variant | G/A;C | snv | 2.4E-05 |
|
Neoplasms | 0.700 | 1.000 | 2 | 2009 | 2012 | |||||||
|
0.851 | 0.080 | 7 | 129210500 | missense variant | G/T | snv |
|
Neoplasms; Nervous System Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
0.701 | 0.200 | 7 | 129206557 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases | 0.810 | 1.000 | 3 | 2014 | 2020 | ||||||||
|
1.000 | 0.080 | 7 | 129213012 | 3 prime UTR variant | C/G;T | snv |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.040 | 7 | 129213282 | 3 prime UTR variant | A/G | snv | 0.15 |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
0.925 | 0.120 | 7 | 129213467 | 3 prime UTR variant | C/A;G | snv |
|
Digestive System Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 |