Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.040 | 14 | 95091236 | stop gained | G/A;C | snv | 4.0E-06 |
|
Neoplasms | 0.700 | 0 | ||||||||||
|
1.000 | 0.040 | 14 | 95111340 | stop gained | G/A | snv |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 95107763 | splice acceptor variant | T/C | snv |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 95104047 | stop gained | C/A | snv |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
0.882 | 0.080 | 14 | 95091289 | missense variant | G/A | snv |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
0.882 | 0.080 | 14 | 95091289 | missense variant | G/A | snv |
|
Endocrine System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 95106075 | frameshift variant | G/- | delins |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 95108022 | frameshift variant | GA/- | del |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 95116458 | frameshift variant | C/- | del |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 95115807 | frameshift variant | C/- | del |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 95116495 | frameshift variant | ATTTT/- | delins |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 95096514 | frameshift variant | GA/- | delins |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
14 | 95105752 | stop gained | G/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||||
|
14 | 95124246 | frameshift variant | -/A | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||||
|
14 | 95103858 | frameshift variant | AAGA/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||||
|
1.000 | 0.040 | 14 | 95105784 | splice acceptor variant | C/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||
|
14 | 95116472 | frameshift variant | -/T | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||||
|
14 | 95099900 | frameshift variant | -/T | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||||
|
14 | 95095936 | frameshift variant | G/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||||
|
1.000 | 0.040 | 14 | 95096461 | frameshift variant | -/T | delins |
|
Neoplasms | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 95096461 | frameshift variant | -/T | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||
|
14 | 95126606 | frameshift variant | T/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||||
|
14 | 95094017 | frameshift variant | A/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||||
|
14 | 95095994 | frameshift variant | ACAA/- | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 | |||||||||||||
|
14 | 95096108 | stop gained | G/T | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms | 0.700 | 0 |