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 | 17 | 50076642 | missense variant | G/A;C | snv | 3.2E-05; 4.0E-06 |
|
0.800 | 0 | ||||||||||||
|
1.000 | 17 | 50075598 | splice acceptor variant | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 17 | 50074452 | missense variant | C/T | snv | 1.2E-05 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | 17 | 50062136 | intron variant | G/A | snv | 0.18 |
|
Nervous System Diseases; Mental Disorders | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.080 | 17 | 50072022 | synonymous variant | C/T | snv | 0.17 | 0.19 |
|
Pathological Conditions, Signs and Symptoms; Neoplasms | 0.020 | 1.000 | 2 | 2011 | 2012 | ||||||
|
0.925 | 0.080 | 17 | 50072022 | synonymous variant | C/T | snv | 0.17 | 0.19 |
|
Neoplasms | 0.020 | 1.000 | 2 | 2011 | 2012 | ||||||
|
0.925 | 0.080 | 17 | 50072022 | synonymous variant | C/T | snv | 0.17 | 0.19 |
|
Pathological Conditions, Signs and Symptoms; Neoplasms | 0.020 | 1.000 | 2 | 2011 | 2012 | ||||||
|
0.925 | 0.080 | 17 | 50072022 | synonymous variant | C/T | snv | 0.17 | 0.19 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1.000 | 17 | 50071380 | missense variant | G/A | snv | 8.0E-06 |
|
0.700 | 1.000 | 2 | 2012 | 2016 | |||||||||
|
0.925 | 0.080 | 17 | 50072022 | synonymous variant | C/T | snv | 0.17 | 0.19 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.925 | 0.080 | 17 | 50072022 | synonymous variant | C/T | snv | 0.17 | 0.19 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
0.882 | 0.040 | 17 | 50063432 | intron variant | C/A;T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.882 | 0.040 | 17 | 50063432 | intron variant | C/A;T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.882 | 0.040 | 17 | 50063432 | intron variant | C/A;T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.882 | 0.040 | 17 | 50063432 | intron variant | C/A;T | snv |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
0.882 | 0.040 | 17 | 50078061 | missense variant | G/A | snv | 0.14 | 9.0E-02 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.882 | 0.040 | 17 | 50078061 | missense variant | G/A | snv | 0.14 | 9.0E-02 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.882 | 0.040 | 17 | 50078061 | missense variant | G/A | snv | 0.14 | 9.0E-02 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.882 | 0.040 | 17 | 50078061 | missense variant | G/A | snv | 0.14 | 9.0E-02 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.882 | 0.040 | 17 | 50073989 | synonymous variant | T/C | snv | 0.21 | 0.24 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.882 | 0.040 | 17 | 50073989 | synonymous variant | T/C | snv | 0.21 | 0.24 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.882 | 0.040 | 17 | 50073989 | synonymous variant | T/C | snv | 0.21 | 0.24 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
0.882 | 0.040 | 17 | 50073989 | synonymous variant | T/C | snv | 0.21 | 0.24 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
1.000 | 17 | 50077024 | missense variant | C/G;T | snv | 8.2E-06 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
1.000 | 17 | 50077122 | splice donor variant | G/A | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 |