Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.040 | 2 | 232535143 | missense variant | G/T | snv |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.040 | 2 | 232531353 | frameshift variant | T/- | del |
|
0.700 | 0 | ||||||||||||
|
0.882 | 0.120 | 9 | 106927699 | stop gained | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.882 | 0.200 | 6 | 33441318 | stop gained | C/T | snv |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.160 | 19 | 38496283 | missense variant | C/G;T | snv | 2.0E-05 |
|
0.700 | 0 | |||||||||||
|
0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.776 | 0.280 | 7 | 140753337 | missense variant | C/A;G;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.160 | 12 | 25227349 | missense variant | C/A;T | snv |
|
0.700 | 0 | ||||||||||||
|
0.662 | 0.440 | 12 | 112450368 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
0.708 | 0.400 | 12 | 112450364 | missense variant | T/A;G | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.701 | 0.240 | 16 | 2176350 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.040 | 14 | 104741231 | missense variant | G/A | snv | 3.4E-05 | 2.8E-05 |
|
0.700 | 0 | ||||||||||
|
0.752 | 0.240 | 4 | 25145092 | synonymous variant | C/T | snv | 2.8E-05 | 4.2E-05 |
|
0.700 | 0 | ||||||||||
|
0.851 | 0.120 | 7 | 19116970 | missense variant | G/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.200 | 8 | 143816981 | stop gained | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.658 | 0.360 | 9 | 83975540 | non coding transcript exon variant | T/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.160 | 6 | 152472395 | frameshift variant | C/- | delins |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.200 | 12 | 116007542 | stop gained | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.763 | 0.200 | 15 | 40729632 | missense variant | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.776 | 0.280 | 19 | 49601646 | frameshift variant | TGCC/- | delins |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.120 | 3 | 49047207 | stop gained | G/A | snv |
|
0.700 | 0 | ||||||||||||
|
0.701 | 0.480 | 4 | 106171094 | splice donor variant | CAGATCTGTCTTTGGAGGATCTGGACACTCAGCAGAGAAATAAGGTGCCGAACTTCTGCCTCCACTGCTGTCAGAAGATGGCTTTGGAGGTTGAGCATGCTGTCTGTAAGTAGCACTTTTAGGAGTCCAACAAAACAGGTTGATAGATTCTCTCACACAGCGTTCAATGTCAATTTC/- | delins |
|
0.700 | 0 | ||||||||||||
|
0.851 | 0.320 | 22 | 42211700 | frameshift variant | -/C | delins |
|
0.700 | 0 | ||||||||||||
|
0.708 | 0.400 | X | 53647576 | splice acceptor variant | T/C | snv |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.200 | 2 | 209819105 | missense variant | G/C | snv | 1.4E-03 | 1.6E-03 |
|
0.700 | 0 |