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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 15 | 66781495 | missense variant | G/A;T | snv | 4.7E-06; 4.7E-06 | 7.0E-06 |
|
0.800 | 0 | |||||||||||
|
1.000 | 15 | 66781288 | missense variant | C/G;T | snv | 8.6E-06 |
|
0.800 | 0 | ||||||||||||
|
15 | 66740813 | non coding transcript exon variant | T/C | snv | 0.78 |
|
0.700 | 1.000 | 3 | 2015 | 2019 | ||||||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.776 | 0.080 | 15 | 66714680 | intron variant | C/G | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
15 | 66743724 | intron variant | T/C | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 15 | 66742474 | intron variant | G/A | snv | 0.41 |
|
Nervous System Diseases; Wounds and Injuries | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
15 | 66719608 | intron variant | T/A;C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
15 | 66707779 | non coding transcript exon variant | C/A;T | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
0.790 | 0.080 | 15 | 66715475 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.790 | 0.080 | 15 | 66715475 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.790 | 0.080 | 15 | 66715475 | intron variant | A/G | snv | 0.26 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.790 | 0.080 | 15 | 66715475 | intron variant | A/G | snv | 0.26 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.790 | 0.080 | 15 | 66715475 | intron variant | A/G | snv | 0.26 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.790 | 0.080 | 15 | 66715475 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.790 | 0.080 | 15 | 66715475 | intron variant | A/G | snv | 0.26 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.790 | 0.080 | 15 | 66715475 | intron variant | A/G | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |