rs28937590
|
0.807 |
0.360 |
2 |
218661219 |
missense variant |
A/G
|
snv
|
4.7E-04
|
4.1E-04
|
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
|
|
0.700 |
1.000 |
2 |
2002 |
2011 |
rs778769841
|
1.000 |
0.200 |
2 |
218661425 |
missense variant |
C/T
|
snv
|
8.4E-05;
4.0E-06
|
4.9E-05
|
Pili torti-deafness syndrome
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
0.700 |
1.000 |
2 |
2007 |
2013 |
rs1057516518
|
1.000 |
0.240 |
2 |
218662963 |
frameshift variant |
-/C
|
delins
|
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
1.000 |
1 |
2009 |
2009 |
rs144885874
|
0.925 |
0.040 |
2 |
218661845 |
missense variant |
C/T
|
snv
|
1.2E-05
|
7.7E-05
|
MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder)
|
Nutritional and Metabolic Diseases
|
0.700 |
1.000 |
1 |
2007 |
2007 |
rs386833856
|
1.000 |
0.240 |
2 |
218661308 |
splice donor variant |
G/C;T
|
snv
|
4.0E-06;
1.2E-05
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
1.000 |
1 |
2002 |
2002 |
rs760559534
|
1.000 |
0.240 |
2 |
218662608 |
frameshift variant |
C/-;CC
|
delins
|
8.0E-06
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs776838028
|
1.000 |
|
2 |
218661896 |
stop gained |
C/T
|
snv
|
4.0E-06
|
3.5E-05
|
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
|
|
0.700 |
1.000 |
1 |
2017 |
2017 |
rs779331797
|
1.000 |
0.240 |
2 |
218661854 |
stop gained |
C/T
|
snv
|
1.2E-05
|
7.0E-06
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs1057516255
|
1.000 |
0.240 |
2 |
218661904 |
frameshift variant |
-/A
|
delins
|
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs1057516346
|
1.000 |
0.240 |
2 |
218662680 |
splice donor variant |
G/A;T
|
snv
|
8.0E-06
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs1057516786
|
1.000 |
0.240 |
2 |
218663369 |
frameshift variant |
AG/-
|
delins
|
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs1057516802
|
1.000 |
0.240 |
2 |
218661954 |
splice donor variant |
G/A
|
snv
|
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs1057516954
|
1.000 |
0.240 |
2 |
218661547 |
splice donor variant |
T/C
|
snv
|
4.0E-06
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs1057517412
|
1.000 |
0.240 |
2 |
218661501 |
frameshift variant |
C/-
|
delins
|
|
7.0E-06
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs1057521059
|
1.000 |
|
2 |
218661470 |
missense variant |
G/A
|
snv
|
|
|
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
|
|
0.700 |
|
0 |
|
|
rs121908572
|
0.882 |
0.280 |
2 |
218661283 |
missense variant |
C/T
|
snv
|
|
|
Leigh Syndrome due to Mitochondrial Complex III Deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs121908576
|
0.851 |
0.360 |
2 |
218661153 |
stop gained |
C/T
|
snv
|
1.7E-04
|
2.9E-04
|
Leigh Disease
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs121908576
|
0.851 |
0.360 |
2 |
218661153 |
stop gained |
C/T
|
snv
|
1.7E-04
|
2.9E-04
|
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
|
|
0.700 |
|
0 |
|
|
rs121908576
|
0.851 |
0.360 |
2 |
218661153 |
stop gained |
C/T
|
snv
|
1.7E-04
|
2.9E-04
|
Pili torti-deafness syndrome
|
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
|
0.700 |
|
0 |
|
|
rs121908578
|
0.882 |
0.200 |
2 |
218661848 |
missense variant |
C/T
|
snv
|
1.8E-04
|
1.0E-04
|
BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
|
|
0.700 |
|
0 |
|
|
rs121908579
|
0.925 |
0.200 |
2 |
218661090 |
missense variant |
G/C
|
snv
|
|
|
BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
|
|
0.700 |
|
0 |
|
|
rs1363475546
|
1.000 |
0.240 |
2 |
218662561 |
frameshift variant |
G/-
|
delins
|
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs1553595997
|
1.000 |
0.240 |
2 |
218661040 |
frameshift variant |
C/-
|
del
|
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs1553596638
|
1.000 |
0.240 |
2 |
218661456 |
frameshift variant |
-/A
|
delins
|
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|
rs1553596761
|
1.000 |
0.240 |
2 |
218661546 |
splice donor variant |
G/A
|
snv
|
|
|
GRACILE SYNDROME (disorder)
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
0.700 |
|
0 |
|
|