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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.040 | 14 | 67727097 | stop gained | C/T | snv |
|
Eye Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 67726144 | missense variant | T/A | snv | 1.2E-05 |
|
Eye Diseases | 0.700 | 0 | ||||||||||
|
0.925 | 0.040 | 14 | 67727056 | missense variant | C/T | snv | 1.6E-05 | 3.5E-05 |
|
Eye Diseases | 0.700 | 0 | |||||||||
|
0.925 | 0.040 | 14 | 67727056 | missense variant | C/T | snv | 1.6E-05 | 3.5E-05 |
|
Eye Diseases | 0.700 | 0 | |||||||||
|
1.000 | 0.040 | 14 | 67726996 | missense variant | C/T | snv | 2.0E-05 | 1.4E-05 |
|
Eye Diseases | 0.700 | 0 | |||||||||
|
0.925 | 0.080 | 14 | 67729248 | missense variant | G/A;T | snv | 8.1E-06; 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.080 | 14 | 67726084 | missense variant | C/T | snv | 1.2E-05 |
|
Eye Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.080 | 14 | 67726084 | missense variant | C/T | snv | 1.2E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.080 | 14 | 67726084 | missense variant | C/T | snv | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 14 | 67724550 | missense variant | C/A;T | snv | 8.0E-06; 1.6E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | ||||||||||
|
0.925 | 0.080 | 14 | 67725206 | missense variant | C/A | snv | 6.4E-05 | 3.5E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||
|
0.882 | 0.080 | 14 | 67729337 | frameshift variant | CCCTG/- | delins | 9.1E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.080 | 14 | 67729337 | frameshift variant | CCCTG/- | delins | 9.1E-05 |
|
Eye Diseases | 0.700 | 0 | ||||||||||
|
0.925 | 0.080 | 14 | 67727191 | splice donor variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 14 | 67727191 | splice donor variant | G/A | snv |
|
Eye Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 14 | 67729308 | frameshift variant | G/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 0 | |||||||||||
|
14 | 67727179 | splice donor variant | GAGGCTCCAAGGTAAGTCTGGAGAAAGAGGA/- | delins |
|
Eye Diseases | 0.700 | 0 | |||||||||||||
|
1.000 | 0.040 | 14 | 67727055 | missense variant | T/C | snv |
|
Eye Diseases | 0.800 | 1.000 | 2 | 2004 | 2004 | ||||||||
|
1.000 | 0.040 | 14 | 67724556 | missense variant | T/A;C | snv |
|
Eye Diseases | 0.800 | 1.000 | 2 | 2004 | 2004 | ||||||||
|
0.925 | 0.080 | 14 | 67726983 | missense variant | C/A;G | snv | 8.0E-06 |
|
Eye Diseases | 0.800 | 1.000 | 2 | 2004 | 2004 | |||||||
|
1.000 | 0.040 | 14 | 67729220 | missense variant | C/G | snv |
|
Eye Diseases | 0.800 | 1.000 | 2 | 2004 | 2004 | ||||||||
|
1.000 | 0.040 | 14 | 67729209 | splice donor variant | A/G | snv | 7.0E-06 |
|
Eye Diseases | 0.800 | 1.000 | 2 | 2004 | 2004 | |||||||
|
0.925 | 0.080 | 14 | 67724550 | missense variant | C/A;T | snv | 8.0E-06; 1.6E-05 |
|
Eye Diseases | 0.800 | 1.000 | 2 | 2004 | 2004 | |||||||
|
0.882 | 0.080 | 14 | 67729337 | frameshift variant | CCCTG/- | delins | 9.1E-05 |
|
0.700 | 1.000 | 1 | 2004 | 2004 | ||||||||
|
0.882 | 0.080 | 14 | 67729337 | frameshift variant | CCCTG/- | delins | 9.1E-05 |
|
Eye Diseases | 0.700 | 1.000 | 1 | 2004 | 2004 |