|
rs121434372
|
|
A |
0.820 |
CausalMutation |
CLINVAR |
Correlation of genotype and phenotype in glutaryl-CoA dehydrogenase deficiency.
|
15505393 |
2004 |
|
rs121434372
|
|
A |
0.820 |
CausalMutation |
CLINVAR |
We report the allele frequencies for three known GA-I LE GCDH variants (M405V, V400M and R227P) and note that both the M405V and V400M variants are significantly more common in the population of African ancestry compared to the general population.
|
27397597 |
2016 |
|
rs121434372
|
|
A |
0.820 |
GeneticVariation |
CLINVAR |
Correlation of genotype and phenotype in glutaryl-CoA dehydrogenase deficiency.
|
15505393 |
2004 |
|
rs121434372
|
|
A |
0.820 |
CausalMutation |
CLINVAR |
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia.
|
21912879 |
2012 |
|
rs121434372
|
|
A |
0.820 |
GeneticVariation |
CLINVAR |
Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the Amish.
|
8900227 |
1996 |
|
rs121434372
|
|
A |
0.820 |
GeneticVariation |
CLINVAR |
Both siblings have high residual glutaryl-CoA dehydrogenase activity, and are compound heterozygotes for two mutations - R227P and V400M reported to be disease-causing in patients with glutaric aciduria type I.
|
9881681 |
1998 |
|
rs121434372
|
|
A |
0.820 |
GeneticVariation |
CLINVAR |
Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutations.
|
9711871 |
1998 |
|
rs121434372
|
|
A |
0.820 |
GeneticVariation |
CLINVAR |
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia.
|
21912879 |
2012 |
|
rs121434372
|
|
A |
0.820 |
CausalMutation |
CLINVAR |
Compound heterozygosity in the glutaryl-CoA dehydrogenase gene with R227P mutation in one allele is associated with no or very low free glutarate excretion.
|
9266361 |
1997 |
|
rs121434372
|
|
A |
0.820 |
CausalMutation |
CLINVAR |
Glutaryl-CoA dehydrogenase deficiency in Spain: evidence of two groups of patients, genetically, and biochemically distinct.
|
10960496 |
2000 |
|
rs121434372
|
|
A |
0.820 |
GeneticVariation |
CLINVAR |
Glutaryl-CoA dehydrogenase deficiency in Spain: evidence of two groups of patients, genetically, and biochemically distinct.
|
10960496 |
2000 |
|
rs567564095
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
|
rs786204626
|
|
A |
0.800 |
GeneticVariation |
CLINVAR |
Correlation of genotype and phenotype in glutaryl-CoA dehydrogenase deficiency.
|
15505393 |
2004 |
|
rs786204626
|
|
A |
0.800 |
GeneticVariation |
CLINVAR |
Molecular determination of glutaric aciduria type I in individuals from southwest Iran.
|
25204480 |
2014 |
|
rs786204626
|
|
A |
0.800 |
GeneticVariation |
CLINVAR |
Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): review and report of thirty novel mutations.
|
9711871 |
1998 |
|
rs786204626
|
|
A |
0.800 |
GeneticVariation |
CLINVAR |
Clinical and mutational spectra of 23 Chinese patients with glutaric aciduria type 1.
|
24332224 |
2014 |
|
rs786204626
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Correlation of genotype and phenotype in glutaryl-CoA dehydrogenase deficiency.
|
15505393 |
2004 |
|
rs786204626
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Extrastriatal changes in patients with late-onset glutaric aciduria type I highlight the risk of long-term neurotoxicity.
|
28438223 |
2017 |
|
rs786204626
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Clinical and mutational spectra of 23 Chinese patients with glutaric aciduria type 1.
|
24332224 |
2014 |
|
rs786204626
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: identification of 3 novel polymorphisms and haplotype definition.
|
10649503 |
2000 |
|
rs786204626
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Mutation analysis of the GCDH gene in Italian and Portuguese patients with glutaric aciduria type I.
|
11073722 |
2000 |
|
rs786204626
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Glutaric aciduria type 1 in South Africa-high incidence of glutaryl-CoA dehydrogenase deficiency in black South Africans.
|
20732827 |
2011 |
|
rs786204626
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the Amish.
|
8900227 |
1996 |
|
rs786204626
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Clinical and laboratory analysis of late-onset glutaric aciduria type I (GA-I) in Uighur: A report of two cases.
|
28352331 |
2017 |
|
rs147611168
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
We report here for the first time on expression studies of four missense mutations c.412A > G (p.Arg138Gly), c.787A > G (p.Met263Val), c.1204C > T (p.Arg402Trp) and c.1240G > A (p.Glu414Lys) identified in GA1 patients in mammalian cells.
|
18775954 |
2008 |