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 | 0.040 | 2 | 222297150 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 20 | 1992 | 2014 | ||||||||
|
1.000 | 0.040 | 2 | 222221369 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 20 | 1992 | 2014 | ||||||||
|
1.000 | 0.040 | 2 | 222297081 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 20 | 1992 | 2014 | ||||||||
|
1.000 | 0.040 | 2 | 222297132 | missense variant | C/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 20 | 1992 | 2014 | ||||||||
|
1.000 | 0.040 | 2 | 222297061 | missense variant | G/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 20 | 1992 | 2014 | ||||||||
|
1.000 | 0.040 | 2 | 222297057 | missense variant | C/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 20 | 1992 | 2014 | ||||||||
|
1.000 | 0.040 | 2 | 222297003 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 19 | 1992 | 2012 | ||||||||
|
1.000 | 0.040 | 2 | 222297160 | missense variant | T/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.810 | 1.000 | 4 | 1993 | 2003 | ||||||||
|
0.925 | 0.040 | 2 | 222297048 | missense variant | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 3 | 1993 | 2003 | ||||||||
|
1.000 | 0.040 | 2 | 222297031 | missense variant | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 3 | 1993 | 2003 | ||||||||
|
0.925 | 0.040 | 2 | 222221300 | frameshift variant | -/C | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 3 | 1995 | 1997 | ||||||||
|
1.000 | 0.040 | 2 | 222232202 | missense variant | C/T | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 3 | 1992 | 2015 | |||||||
|
1.000 | 0.040 | 2 | 222297157 | missense variant | C/A;G;T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 2 | 2014 | 2018 | ||||||||
|
1.000 | 0.040 | 2 | 222221362 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.200 | 2 | 222297158 | missense variant | G/C | snv |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases | 0.800 | 1.000 | 1 | 1996 | 1996 | ||||||||
|
1.000 | 0.040 | 2 | 222232080 | stop gained | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 2 | 222232131 | frameshift variant | AATGTCAGGGTAA/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 2 | 222294289 | frameshift variant | C/- | del |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 2 | 222297139 | inframe deletion | GTTGGGCAGCGG/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 2 | 222221236 | missense variant | G/A;T | snv | 4.0E-06; 2.7E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.010 | 1.000 | 1 | 1998 | 1998 | |||||||
|
0.882 | 0.040 | 2 | 222202200 | intron variant | C/G;T | snv | 0.11; 2.6E-05 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.882 | 0.040 | 2 | 222202200 | intron variant | C/G;T | snv | 0.11; 2.6E-05 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.882 | 0.040 | 2 | 222202200 | intron variant | C/G;T | snv | 0.11; 2.6E-05 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.080 | 2 | 222294286 | missense variant | C/A;T | snv | 1.2E-05 |
|
Eye Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 222297175 | missense variant | C/A;G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2018 | 2018 |