DSTYK, dual serine/threonine and tyrosine protein kinase, 25778
N. diseases: 42; N. variants: 33
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 | 205161285 | missense variant | A/G;T | snv | 0.93 |
|
0.700 | 1.000 | 2 | 2018 | 2019 | ||||||||||
|
1 | 205158931 | intron variant | C/T | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205175877 | intron variant | C/T | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205184080 | intron variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
1 | 205184184 | intron variant | G/A | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205187972 | intron variant | T/C | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205189055 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
1 | 205193929 | intron variant | A/G | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205212398 | upstream gene variant | T/C | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205145971 | 3 prime UTR variant | G/A | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205149208 | intron variant | T/G | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205177332 | intron variant | A/G | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205203047 | intron variant | C/T | snv | 0.49 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205203973 | intron variant | A/G | snv | 0.49 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205208489 | intron variant | G/A | snv | 0.49 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205210329 | intron variant | A/G | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205175235 | intron variant | G/T | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1 | 205195452 | intron variant | C/T | snv | 0.45 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205194670 | intron variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
1 | 205195522 | intron variant | A/G | snv | 0.49 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205153401 | intron variant | A/G | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 0.080 | 1 | 205211450 | missense variant | C/T | snv | 1.0E-03 | 6.6E-04 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
1 | 205211934 | upstream gene variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
1 | 205142633 | 3 prime UTR variant | A/C | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1 | 205186625 | intron variant | C/T | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |