Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 2 | 165313924 | missense variant | C/G;T | snv | 4.0E-06 | 0.700 | 0 | ||||||||
|
1 | 1.000 | 2 | 165344627 | missense variant | G/A | snv | 0.700 | 0 | |||||||||
|
1 | 1.000 | 2 | 165344707 | missense variant | G/C | snv | 0.700 | 0 | |||||||||
|
4 | 0.882 | 0.080 | 2 | 165354232 | missense variant | G/T | snv | 0.800 | 0 | ||||||||
|
2 | 0.925 | 0.040 | 2 | 165373322 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 2 | 165374689 | missense variant | T/A | snv | 0.700 | 0 | |||||||||
|
5 | 0.827 | 0.080 | 2 | 165374737 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 2 | 165389123 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 2 | 165308795 | splice donor variant | G/A;T | snv | 0.700 | 0 | |||||||||
|
2 | 0.925 | 0.080 | 2 | 165313732 | stop gained | C/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 2 | 165314014 | missense variant | A/C;G | snv | 0.700 | 0 | |||||||||
|
2 | 0.925 | 0.080 | 2 | 165344801 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 2 | 165388647 | missense variant | T/C | snv | 0.700 | 0 | |||||||||
|
4 | 0.925 | 0.160 | 2 | 165386920 | stop gained | G/A;T | snv | 0.700 | 0 | ||||||||
|
6 | 0.882 | 0.080 | 2 | 165313738 | frameshift variant | T/- | delins | 0.700 | 0 |