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 | 0.160 | 10 | 124408601 | missense variant | C/A;T | snv | 8.0E-06 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.851 | 0.160 | 10 | 124408601 | missense variant | C/A;T | snv | 8.0E-06 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.851 | 0.160 | 10 | 124408601 | missense variant | C/A;T | snv | 8.0E-06 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.851 | 0.160 | 10 | 124408601 | missense variant | C/A;T | snv | 8.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Neoplasms | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.925 | 0.080 | 10 | 124403892 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||
|
0.882 | 0.080 | 10 | 124412125 | missense variant | C/G;T | snv | 2.4E-05; 3.2E-05 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.882 | 0.080 | 10 | 124412125 | missense variant | C/G;T | snv | 2.4E-05; 3.2E-05 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.882 | 0.080 | 10 | 124412125 | missense variant | C/G;T | snv | 2.4E-05; 3.2E-05 |
|
Pathological Conditions, Signs and Symptoms; Neoplasms | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
0.882 | 0.080 | 10 | 124412125 | missense variant | C/G;T | snv | 2.4E-05; 3.2E-05 |
|
Neoplasms; Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2003 | 2003 | |||||||
|
10 | 124400877 | frameshift variant | T/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2005 | 2005 | ||||||||||
|
1.000 | 0.080 | 10 | 124408917 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.080 | 10 | 124403892 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 |
|
Male Urogenital Diseases | 0.020 | 1.000 | 2 | 2005 | 2015 | ||||||
|
1.000 | 0.080 | 10 | 124412009 | missense variant | A/G | snv | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | |||||||
|
1.000 | 0.080 | 10 | 124408887 | missense variant | C/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | ||||||||
|
0.851 | 0.160 | 10 | 124408601 | missense variant | C/A;T | snv | 8.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | |||||||
|
1.000 | 0.080 | 10 | 124403019 | missense variant | C/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | ||||||||
|
1.000 | 0.080 | 10 | 124403015 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | ||||||||
|
1.000 | 0.080 | 10 | 124400875 | missense variant | C/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | ||||||||
|
1.000 | 0.080 | 10 | 124403835 | missense variant | T/C | snv | 4.0E-06 | 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | ||||||
|
1.000 | 0.080 | 10 | 124412010 | missense variant | G/T | snv | 1.2E-05 | 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | ||||||
|
1.000 | 0.080 | 10 | 124401785 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | ||||||||
|
1.000 | 0.080 | 10 | 124403820 | missense variant | C/G;T | snv | 4.8E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | |||||||
|
1.000 | 0.080 | 10 | 124400941 | missense variant | C/T | snv | 4.0E-05 | 7.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | ||||||
|
1.000 | 0.080 | 10 | 124398082 | missense variant | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 | ||||||||
|
1.000 | 0.080 | 10 | 124408897 | missense variant | G/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases | 0.700 | 1.000 | 7 | 1988 | 2013 |