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 | 0.040 | 2 | 96254107 | missense variant | A/G | snv | 0.800 | 1.000 | 0 | 2010 | 2014 | |||||
|
1 | 1.000 | 0.040 | 2 | 96254106 | missense variant | C/A;T | snv | 4.0E-06 | 0.800 | 1.000 | 0 | 2010 | 2014 | ||||
|
1 | 1.000 | 0.040 | 2 | 96265399 | 5 prime UTR variant | G/A | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.040 | 2 | 96265379 | start lost | C/A;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 2 | 96265306 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.080 | 2 | 96265262 | frameshift variant | ACAG/- | delins | 2.1E-05 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.040 | 2 | 96265232 | frameshift variant | -/T | delins | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 2 | 96254998 | splice acceptor variant | C/A;G | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.080 | 2 | 96254974 | frameshift variant | TCTG/- | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 2 | 96254832 | splice donor variant | C/A | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 2 | 96254117 | splice acceptor variant | T/C;G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 2 | 96254078 | stop gained | C/T | snv | 0.700 | 0 | ||||||||
|
3 | 0.925 | 0.040 | 2 | 96254050 | stop gained | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.040 | 2 | 96253884 | frameshift variant | -/TCTGAGAGCAGCTC | delins | 4.0E-06 | 0.700 | 0 |