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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 0.925 | 0.120 | 11 | 103129005 | splice region variant | G/A | snv | 4.2E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 103199400 | missense variant | T/C | snv | 8.1E-06 | 5.6E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.120 | 11 | 103236479 | frameshift variant | AAAAG/- | delins | 4.0E-06 | 1.4E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.120 | 11 | 103121029 | frameshift variant | TTAA/- | delins | 2.8E-05 | 0.700 | 0 | |||||||
|
8 | 1.000 | 0.120 | 11 | 103125293 | stop gained | C/T | snv | 4.5E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 103135524 | stop gained | G/A | snv | 1.4E-05 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 11 | 103192150 | missense variant | C/A;T | snv | 5.1E-06; 5.1E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 11 | 103185032 | missense variant | G/A | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 103177605 | frameshift variant | T/- | delins | 7.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.120 | 11 | 103120693 | frameshift variant | TGGAAAGCTG/- | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103133640 | frameshift variant | -/T | delins | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 11 | 103135630 | missense variant | T/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103152284 | frameshift variant | A/- | del | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.120 | 11 | 103158709 | inframe insertion | -/GTCACAACA | delins | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103160931 | splice acceptor variant | G/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103160971 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103163089 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103174108 | frameshift variant | C/- | del | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103179047 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103203777 | splice donor variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103204944 | frameshift variant | T/- | del | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103211839 | frameshift variant | G/- | del | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103253347 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103311981 | frameshift variant | G/- | del | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 11 | 103479135 | missense variant | T/C | snv | 0.700 | 0 |