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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
15 | 88871064 | intron variant | G/T | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
15 | 88871064 | intron variant | G/T | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
15 | 88852395 | intron variant | A/G | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
15 | 88854874 | synonymous variant | C/T | snv | 0.50 | 0.48 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
15 | 88854874 | synonymous variant | C/T | snv | 0.50 | 0.48 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
15 | 88854596 | intron variant | A/G | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 88854596 | intron variant | A/G | snv | 0.11 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 88872016 | missense variant | C/G | snv | 0.20 | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
15 | 88872016 | missense variant | C/G | snv | 0.20 | 0.20 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
15 | 88872016 | missense variant | C/G | snv | 0.20 | 0.20 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
15 | 88806477 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
15 | 88827235 | intron variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 88842993 | intron variant | T/C | snv | 6.3E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
15 | 88817911 | intron variant | A/G | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
15 | 88806225 | intron variant | A/C | snv | 1.7E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
15 | 88816458 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 1 | 2008 | 2008 | |||||||||||
|
15 | 88855400 | missense variant | T/A | snv | 0.51 | 0.52 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
15 | 88811655 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
1.000 | 0.080 | 15 | 88856723 | missense variant | G/T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | 15 | 88857646 | missense variant | T/A | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.040 | 15 | 88872944 | missense variant | G/A | snv | 8.0E-06 |
|
0.700 | 0 |