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 | 14 | 64823094 | start lost | T/C | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.080 | 14 | 64767812 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.700 | 0 | ||||||||||
|
1.000 | 14 | 64784333 | stop gained | G/A;T | snv | 4.0E-06; 4.0E-06 |
|
0.700 | 0 | ||||||||||||
|
1.000 | 0.080 | 14 | 64767686 | frameshift variant | -/AA | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 14 | 64767787 | missense variant | A/G | snv |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 14 | 64767787 | missense variant | A/G | snv |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 14 | 64767787 | missense variant | A/G | snv |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 14 | 64767787 | missense variant | A/G | snv |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 14 | 64767787 | missense variant | A/G | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.040 | 14 | 64770879 | splice donor variant | ACCTGGGCCTC/- | delins |
|
Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 14 | 64771060 | stop gained | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 14 | 64774392 | splice region variant | C/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 14 | 64787102 | stop gained | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 14 | 64801754 | missense variant | C/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.080 | 14 | 64782493 | stop gained | C/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 14 | 64772867 | stop gained | G/A | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 14 | 64794466 | splice donor variant | C/T | snv |
|
0.700 | 0 | |||||||||||||
|
1.000 | 0.080 | 14 | 64767300 | splice region variant | C/A | snv |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 14 | 64767745 | frameshift variant | -/TC | delins |
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 14 | 64793751 | frameshift variant | G/- | del |
|
0.700 | 0 | |||||||||||||
|
0.925 | 0.080 | 14 | 64828210 | intron variant | G/A | snv | 0.12 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.080 | 14 | 64828210 | intron variant | G/A | snv | 0.12 |
|
Neoplasms; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2013 | 2013 |