Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 21018633 | intron variant | A/G | snv | 0.14 |
|
0.800 | 1.000 | 2 | 2012 | 2019 | ||||||||||
|
2 | 21018633 | intron variant | A/G | snv | 0.14 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | ||||||||||
|
2 | 21044589 | upstream gene variant | G/A | snv | 0.25 |
|
0.700 | 1.000 | 2 | 2012 | 2012 | ||||||||||
|
2 | 21044589 | upstream gene variant | G/A | snv | 0.25 |
|
0.700 | 1.000 | 2 | 2012 | 2012 | ||||||||||
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.800 | 1.000 | 1 | 2011 | 2012 | ||||||||||
|
2 | 21021128 | intron variant | G/T | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | |||||||||
|
2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
2 | 21009932 | synonymous variant | G/A | snv | 0.39 | 0.38 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | |||||||||
|
2 | 21017492 | intron variant | A/G | snv | 0.73 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21017159 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
2 | 21026844 | missense variant | C/T | snv | 2.7E-02 | 2.7E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
2 | 21026844 | missense variant | C/T | snv | 2.7E-02 | 2.7E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
2 | 21026844 | missense variant | C/T | snv | 2.7E-02 | 2.7E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
2 | 21018633 | intron variant | A/G | snv | 0.14 |
|
0.800 | 1.000 | 1 | 2012 | 2019 | ||||||||||
|
2 | 21042823 | intron variant | T/C | snv | 3.8E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21042823 | intron variant | T/C | snv | 3.8E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21042823 | intron variant | T/C | snv | 3.8E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21018872 | intron variant | C/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21018872 | intron variant | C/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
2 | 21018872 | intron variant | C/T | snv | 0.13 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |