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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 0.925 | 0.160 | 7 | 107663412 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
3 | 0.925 | 0.160 | 7 | 107710192 | stop gained | T/A;C | snv | 0.700 | 0 | ||||||||
|
1 | 7 | 107663430 | missense variant | T/C | snv | 1.4E-05 | 0.700 | 0 | |||||||||
|
4 | 0.925 | 0.160 | 7 | 107690203 | missense variant | C/G;T | snv | 4.0E-06; 1.8E-04 | 0.700 | 0 | |||||||
|
4 | 0.925 | 0.160 | 7 | 107690200 | missense variant | G/A;C | snv | 1.0E-04; 8.0E-06 | 0.700 | 0 | |||||||
|
4 | 0.925 | 0.160 | 7 | 107698112 | splice donor variant | G/A;C;T | snv | 1.6E-05; 4.0E-06 | 0.700 | 0 | |||||||
|
4 | 0.925 | 0.160 | 7 | 107683453 | splice acceptor variant | A/G | snv | 3.6E-04 | 1.7E-04 | 0.700 | 0 | ||||||
|
3 | 0.925 | 0.160 | 7 | 107702050 | missense variant | T/A | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 7 | 107674337 | stop gained | G/A;T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
5 | 0.882 | 0.280 | 7 | 107710132 | missense variant | A/G | snv | 1.2E-04 | 3.5E-05 | 0.700 | 0 | ||||||
|
4 | 0.925 | 0.160 | 7 | 107710126 | missense variant | C/T | snv | 5.2E-05 | 2.8E-05 | 0.700 | 0 | ||||||
|
3 | 0.925 | 0.160 | 7 | 107689166 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 7 | 107694478 | stop gained | A/G;T | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
2 | 1.000 | 0.120 | 7 | 107704370 | missense variant | T/C;G | snv | 4.4E-06 | 0.700 | 0 | |||||||
|
3 | 0.925 | 0.160 | 7 | 107690199 | missense variant | C/T | snv | 1.6E-05 | 0.700 | 0 | |||||||
|
2 | 1.000 | 0.120 | 7 | 107661723 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 7 | 107663357 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 7 | 107674944 | splice acceptor variant | G/A | snv | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.160 | 7 | 107698076 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 7 | 107700115 | frameshift variant | -/T | delins | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 7 | 107701069 | intron variant | TAAGTAACTTGACATTT/- | delins | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 7 | 107710069 | frameshift variant | -/GCTGG | delins | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 7 | 107694457 | stop gained | A/T | snv | 0.700 | 0 | ||||||||
|
2 | 1.000 | 0.120 | 7 | 107694478 | frameshift variant | A/- | delins | 0.700 | 0 | ||||||||
|
4 | 0.925 | 0.160 | 7 | 107700180 | splice region variant | G/A | snv | 8.0E-06 | 1.4E-05 | 0.700 | 0 |