rs118203997
|
1.000 |
0.120 |
16 |
23634893 |
stop gained |
A/G;T
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs118203998
|
0.790 |
0.400 |
16 |
23603471 |
stop gained |
G/C;T
|
snv
|
1.6E-05;
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs118203999
|
0.925 |
0.200 |
16 |
23623003 |
stop gained |
G/A
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs180177085
|
0.925 |
0.200 |
16 |
23636151 |
frameshift variant |
A/-
|
del
|
8.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs180177092
|
0.851 |
0.280 |
16 |
23635788 |
frameshift variant |
AG/-
|
delins
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs180177100
|
0.827 |
0.400 |
16 |
23635306 |
stop gained |
G/A
|
snv
|
8.0E-06
|
1.4E-05
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs180177113
|
1.000 |
0.120 |
16 |
23629760 |
frameshift variant |
-/AG
|
ins
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs180177116
|
1.000 |
0.120 |
16 |
23629269 |
frameshift variant |
T/-
|
delins
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs180177133
|
0.807 |
0.240 |
16 |
23614089 |
frameshift variant |
T/-
|
delins
|
1.2E-05
|
1.4E-05
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs180177135
|
0.716 |
0.520 |
16 |
23607891 |
frameshift variant |
T/-
|
del
|
|
2.1E-05
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs515726073
|
1.000 |
0.120 |
16 |
23634869 |
frameshift variant |
TT/C;T
|
delins
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs587776419
|
0.882 |
0.200 |
16 |
23624008 |
splice donor variant |
C/A;G;T
|
snv
|
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|
rs757369748
|
0.882 |
0.200 |
16 |
23638072 |
stop gained |
G/A;T
|
snv
|
4.0E-06
|
|
FANCONI ANEMIA, COMPLEMENTATION GROUP N
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
|
0.700 |
|
0 |
|
|