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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 54560455 | intron variant | C/G | snv | 7.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
2 | 54533683 | intron variant | T/C | snv | 0.77 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
2 | 54457261 | 5 prime UTR variant | C/T | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
2 | 54572462 | intron variant | G/T | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
2 | 54457420 | intron variant | A/G | snv | 0.76 |
|
Wounds and Injuries | 0.020 | 1.000 | 2 | 2010 | 2013 | |||||||||
|
2 | 54655541 | intron variant | G/A | snv | 0.28 |
|
Wounds and Injuries | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
2 | 54654484 | intron variant | T/C | snv | 0.64 |
|
Wounds and Injuries | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1.000 | 0.040 | 2 | 54491044 | intron variant | T/A;C | snv |
|
Eye Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.040 | 2 | 54538037 | intron variant | G/A | snv | 0.29 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54540655 | non coding transcript exon variant | A/G | snv | 9.9E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54539021 | intron variant | C/A | snv | 0.12 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54535599 | intron variant | T/G | snv | 0.80 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54553416 | intron variant | T/C | snv | 0.81 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54552097 | intron variant | T/C | snv | 0.81 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54538015 | intron variant | G/A;C | snv | 0.80 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54553737 | intron variant | C/G | snv | 0.15 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54552141 | intron variant | T/G | snv | 0.80 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54550783 | intron variant | T/C | snv | 9.4E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54542506 | intron variant | C/G;T | snv |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.040 | 2 | 54546618 | non coding transcript exon variant | A/T | snv | 0.81 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54541531 | intron variant | A/G | snv | 0.71 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54570661 | intron variant | C/T | snv | 0.27 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54553641 | intron variant | A/T | snv | 5.8E-02 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54546704 | intron variant | T/A | snv | 0.30 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 2 | 54622367 | missense variant | T/C | snv | 4.0E-06 |
|
Mental Disorders | 0.010 | 1.000 | 1 | 2016 | 2016 |