SHANK3, SH3 and multiple ankyrin repeat domains 3, 85358
N. diseases: 169; N. variants: 24
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
22 | 50712045 | intron variant | G/A | snv | 0.20 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 2 | 2019 | 2019 | |||||||||
|
22 | 50673933 | intron variant | G/A;C;T | snv |
|
0.700 | 1.000 | 2 | 2016 | 2017 | |||||||||||
|
1.000 | 0.040 | 22 | 50719589 | intron variant | G/C | snv | 0.52 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||||
|
22 | 50682988 | intron variant | T/G | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1.000 | 0.040 | 22 | 50695096 | intron variant | C/A;T | snv | 2.0E-02 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
1.000 | 0.040 | 22 | 50678709 | intron variant | G/A | snv | 0.35 | 0.36 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
1.000 | 0.040 | 22 | 50678709 | intron variant | G/A | snv | 0.35 | 0.36 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.040 | 22 | 50678709 | intron variant | G/A | snv | 0.35 | 0.36 |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
22 | 50710567 | intron variant | G/A | snv | 0.19 |
|
Behavior and Behavior Mechanisms | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 22 | 50676625 | stop gained | C/T | snv |
|
Pathological Conditions, Signs and Symptoms; Nervous System Diseases | 0.700 | 0 | ||||||||||||
|
1.000 | 22 | 50676625 | stop gained | C/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 22 | 50721182 | stop gained | C/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.080 | 22 | 50678666 | missense variant | C/G | snv |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.800 | 1.000 | 3 | 2013 | 2013 | ||||||||
|
1.000 | 0.040 | 22 | 50674675 | missense variant | C/T | snv |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 22 | 50683352 | missense variant | C/T | snv | 1.1E-04 | 3.5E-05 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1.000 | 22 | 50698797 | missense variant | C/A;G;T | snv | 4.1E-06 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
0.925 | 0.040 | 22 | 50720865 | missense variant | G/C;T | snv | 1.1E-03 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
0.925 | 0.040 | 22 | 50720865 | missense variant | G/C;T | snv | 1.1E-03 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 22 | 50679152 | missense variant | T/C | snv | 0.43 | 0.46 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
1.000 | 0.040 | 22 | 50679152 | missense variant | T/C | snv | 0.43 | 0.46 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||||
|
1.000 | 0.080 | 22 | 50684651 | missense variant | G/T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | 22 | 50684651 | missense variant | G/T | snv |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 22 | 50715048 | splice donor variant | G/A | snv | 7.0E-06 |
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities | 0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 22 | 50721505 | frameshift variant | G/-;GG | delins |
|
Mental Disorders | 0.700 | 1.000 | 2 | 2015 | 2019 | ||||||||
|
0.925 | 0.120 | 22 | 50721257 | frameshift variant | CT/- | del |
|
Mental Disorders | 0.700 | 1.000 | 1 | 2019 | 2019 |