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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 10 | 100216744 | intron variant | G/C | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 3 | 100894935 | intron variant | C/T | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.080 | 15 | 101446425 | intron variant | G/T | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 15 | 101854599 | downstream gene variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.080 | 13 | 102066314 | intron variant | A/G | snv | 5.9E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 5 | 102284470 | intron variant | T/C | snv | 0.81 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.080 | 7 | 102743216 | intron variant | T/A | snv | 0.35 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 5 | 102764872 | intron variant | C/T | snv | 3.1E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 5 | 102912212 | intron variant | A/T | snv | 6.8E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 5 | 103003035 | missense variant | C/G;T | snv | 3.7E-03; 8.1E-06 |
|
0.710 | 1.000 | 1 | 2014 | 2018 | ||||||||
|
1.000 | 0.080 | 5 | 103003107 | missense variant | A/G | snv | 3.1E-02 | 3.2E-02 |
|
0.710 | 1.000 | 1 | 2014 | 2018 | |||||||
|
1.000 | 0.080 | 4 | 103067742 | intron variant | G/A;T | snv |
|
0.800 | 1.000 | 2 | 2011 | 2018 | |||||||||
|
1.000 | 0.080 | 5 | 103087264 | 3 prime UTR variant | C/T | snv | 3.2E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 5 | 103250706 | intron variant | G/A | snv | 3.0E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 7 | 103778399 | intron variant | C/T | snv | 0.41 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 8 | 104548593 | intron variant | A/G | snv | 1.6E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.080 | 7 | 105603002 | upstream gene variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.080 | 18 | 10695159 | intron variant | A/G | snv | 0.36 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
1.000 | 0.080 | 8 | 107059816 | intergenic variant | G/A;C;T | snv |
|
0.700 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
1.000 | 0.080 | 6 | 107256268 | intron variant | G/A | snv | 8.5E-02 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.080 | 9 | 107268309 | intergenic variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.080 | 20 | 10771962 | intron variant | C/T | snv | 0.22 |
|
0.710 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.080 | 8 | 10775649 | intron variant | A/C | snv | 0.60 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 12 | 108219374 | intron variant | G/A | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 12 | 108224853 | missense variant | C/T | snv | 0.27 | 0.20 |
|
0.700 | 1.000 | 1 | 2018 | 2018 |