EYA1, EYA transcriptional coactivator and phosphatase 1, 2138
N. diseases: 168; N. variants: 36
Source: ALL
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 | 8 | 71216733 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 11 | 1997 | 2017 | ||||||||
|
0.882 | 0.040 | 8 | 71216776 | missense variant | C/T | snv | 1.4E-04 | 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.710 | 1.000 | 7 | 1997 | 2018 | ||||||
|
1.000 | 0.040 | 8 | 71215630 | missense variant | A/G | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 6 | 1997 | 2011 | |||||||
|
1.000 | 0.040 | 8 | 71215470 | missense variant | A/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 6 | 1997 | 2011 | ||||||||
|
0.882 | 0.040 | 8 | 71199371 | missense variant | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 6 | 1997 | 2011 | ||||||||
|
0.925 | 0.040 | 8 | 71244662 | stop gained | G/A;T | snv | 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 4 | 2006 | 2016 | |||||||
|
1.000 | 0.040 | 8 | 71271835 | stop gained | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 2 | 2000 | 2008 | ||||||||
|
8 | 71199443 | intron variant | T/C | snv | 0.40 | 0.35 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
8 | 71495139 | intron variant | G/C | snv | 6.2E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
8 | 71495139 | intron variant | G/C | snv | 6.2E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
8 | 71382353 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||||
|
0.925 | 0.040 | 8 | 71211215 | missense variant | T/C | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2000 | 2000 | ||||||||
|
1.000 | 0.040 | 8 | 71244656 | missense variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2000 | 2000 | ||||||||
|
0.882 | 0.040 | 8 | 71216776 | missense variant | C/T | snv | 1.4E-04 | 1.4E-05 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
|
8 | 71580003 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||||
|
1.000 | 0.040 | 8 | 71216853 | splice acceptor variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||
|
1.000 | 0.040 | 8 | 71220245 | intron variant | C/A | snv |
|
Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
8 | 71483978 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
8 | 71335939 | intron variant | T/C | snv | 0.33 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2008 | 2008 | |||||||||
|
8 | 71557507 | intron variant | A/G | snv | 0.41 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
8 | 71557507 | intron variant | A/G | snv | 0.41 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
8 | 71557507 | intron variant | A/G | snv | 0.41 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.882 | 0.120 | 8 | 71271753 | splice region variant | C/T | snv |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.882 | 0.120 | 8 | 71271753 | splice region variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
0.882 | 0.120 | 8 | 71271753 | splice region variant | C/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 1.000 | 1 | 2017 | 2017 |