PRKN, parkin RBR E3 ubiquitin protein ligase, 5071
N. diseases: 42; N. variants: 45
Source: CURATED ×
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 162612318 | intron variant | A/G | snv | 8.7E-02 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | ||||||||||
|
0.882 | 0.040 | 6 | 161785877 | missense variant | G/A | snv | 4.2E-04 | 4.5E-04 |
|
0.700 | 1.000 | 4 | 2003 | 2018 | |||||||
|
0.752 | 0.200 | 6 | 161785820 | missense variant | G/A;T | snv | 1.9E-03; 8.0E-06 |
|
0.700 | 1.000 | 4 | 2003 | 2018 | ||||||||
|
0.882 | 0.040 | 6 | 162443356 | missense variant | C/A;G;T | snv | 3.2E-05; 2.6E-04 |
|
0.700 | 1.000 | 4 | 2003 | 2018 | ||||||||
|
0.925 | 0.040 | 6 | 161785805 | missense variant | C/A;T | snv | 4.0E-06; 1.6E-04 |
|
0.700 | 1.000 | 4 | 2003 | 2018 | ||||||||
|
6 | 162612318 | intron variant | A/G | snv | 8.7E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
6 | 161689529 | intron variant | G/A | snv | 9.8E-05 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
6 | 161699571 | intron variant | C/A | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||||
|
6 | 162560234 | intron variant | C/A;G | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
0.925 | 0.040 | 6 | 162636237 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
6 | 161800688 | intron variant | A/G | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
6 | 162588303 | intron variant | G/A | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
6 | 161726695 | intron variant | A/T | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
0.925 | 0.040 | 6 | 161900345 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
6 | 161580404 | intron variant | T/C | snv | 0.71 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||||
|
6 | 161580404 | intron variant | T/C | snv | 0.71 |
|
0.700 | 1.000 | 1 | 2008 | 2008 | ||||||||||
|
0.752 | 0.200 | 6 | 161785820 | missense variant | G/A;T | snv | 1.9E-03; 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 6 | 161785885 | missense variant | C/A;T | snv | 1.6E-05 |
|
0.700 | 0 | ||||||||||||
|
6 | 162612318 | intron variant | A/G | snv | 8.7E-02 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.120 | 6 | 162250424 | intron variant | A/T | snv | 2.1E-02 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.080 | 6 | 162379633 | intron variant | C/T | snv | 0.22 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 6 | 161931643 | intron variant | G/A | snv | 1.3E-02 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.040 | 6 | 162636237 | intron variant | T/A;C | snv |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.040 | 6 | 161740587 | intron variant | C/T | snv | 0.67 |
|
Musculoskeletal Diseases | 0.800 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.040 | 6 | 161900345 | intron variant | A/G;T | snv |
|
Musculoskeletal Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 |