rs11711441
|
1.000 |
0.040 |
3 |
183103487 |
intron variant |
G/A
|
snv
|
|
0.12
|
Parkinson Disease
|
Nervous System Diseases
|
0.810 |
1.000 |
4 |
2011 |
2013 |
rs762463914
|
1.000 |
0.120 |
3 |
183099440 |
start lost |
T/C
|
snv
|
1.8E-05
|
3.5E-05
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs199517715
|
1.000 |
0.120 |
3 |
183092545 |
missense variant |
C/T
|
snv
|
4.0E-05
|
3.5E-05
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
11 |
2001 |
2016 |
rs1057520695
|
1.000 |
0.120 |
3 |
183092514 |
missense variant |
G/C
|
snv
|
|
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
11 |
2001 |
2016 |
rs1311374961
|
1.000 |
0.120 |
3 |
183092510 |
frameshift variant |
CT/-
|
delins
|
4.0E-06
|
1.4E-05
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs754460336
|
1.000 |
0.120 |
3 |
183092486 |
missense variant |
G/A
|
snv
|
6.4E-05
|
5.6E-05
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs920162850
|
1.000 |
0.120 |
3 |
183086719 |
stop gained |
G/A
|
snv
|
|
7.0E-06
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs9822789
|
1.000 |
0.040 |
3 |
183085086 |
intron variant |
G/T
|
snv
|
|
0.17
|
Parkinson Disease
|
Nervous System Diseases
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs12638619
|
1.000 |
0.040 |
3 |
183081454 |
intron variant |
C/T
|
snv
|
|
0.17
|
Parkinson Disease
|
Nervous System Diseases
|
0.700 |
1.000 |
1 |
2011 |
2011 |
rs202197951
|
1.000 |
0.120 |
3 |
183072469 |
missense variant |
C/T
|
snv
|
1.2E-05
|
2.1E-05
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
11 |
2001 |
2016 |
rs1229069160
|
1.000 |
0.120 |
3 |
183072457 |
missense variant |
C/T
|
snv
|
|
7.0E-06
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs748201122
|
1.000 |
0.120 |
3 |
183071310 |
missense variant |
C/A;T
|
snv
|
4.0E-06
|
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs757362635
|
1.000 |
0.120 |
3 |
183071290 |
missense variant |
A/G;T
|
snv
|
2.4E-05;
1.2E-05
|
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs186209189
|
1.000 |
0.120 |
3 |
183071223 |
missense variant |
C/A;T
|
snv
|
4.0E-06;
8.0E-06
|
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
11 |
2001 |
2016 |
rs199914879
|
1.000 |
0.120 |
3 |
183071208 |
splice donor variant |
A/T
|
snv
|
8.0E-06
|
1.4E-05
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs772395858
|
1.000 |
0.120 |
3 |
183071122 |
splice acceptor variant |
T/C
|
snv
|
8.0E-06
|
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
4 |
2001 |
2016 |
rs886058209
|
1.000 |
0.120 |
3 |
183071119 |
splice acceptor variant |
CC/-
|
delins
|
4.0E-06
|
1.4E-05
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs727504004
|
1.000 |
0.120 |
3 |
183071066 |
missense variant |
G/A
|
snv
|
|
7.0E-06
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs1560256569
|
1.000 |
0.120 |
3 |
183071018 |
stop gained |
TCTC/GCTATGCTAT
|
delins
|
|
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs773433541
|
1.000 |
0.120 |
3 |
183057358 |
missense variant |
A/C;G
|
snv
|
8.1E-06
|
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs185741664
|
1.000 |
0.120 |
3 |
183057343 |
stop gained |
G/A
|
snv
|
4.5E-05
|
2.1E-05
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs754437245
|
1.000 |
0.120 |
3 |
183057342 |
missense variant |
C/T
|
snv
|
1.6E-05
|
7.0E-06
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
11 |
2001 |
2016 |
rs746500530
|
1.000 |
0.120 |
3 |
183057321 |
missense variant |
T/C
|
snv
|
2.5E-05
|
1.4E-05
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
11 |
2001 |
2016 |
rs1326114075
|
1.000 |
0.120 |
3 |
183057318 |
missense variant |
G/A
|
snv
|
|
7.0E-06
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs201041864
|
1.000 |
0.120 |
3 |
183057312 |
missense variant |
G/A
|
snv
|
1.4E-04
|
1.0E-04
|
3-methylcrotonyl CoA carboxylase 1 deficiency
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
11 |
2001 |
2016 |