rs104894106
|
|
|
0.810 |
GeneticVariation |
BEFREE |
The point mutations I154F and W155R in frataxin cause FRDA and are clustered to one surface of the protein, and these mutations decrease the interaction of frataxin with ISD11.
|
17331979 |
2007 |
rs146818694
|
|
|
0.720 |
GeneticVariation |
BEFREE |
The genotypic and phenotypic spectrum of FRDA was similar to other populations, with one patient compound heterozygote for a known point mutation in FXN (Asn146Lys).
|
24209901 |
2014 |
rs146818694
|
|
|
0.720 |
GeneticVariation |
BEFREE |
To reinvestigate the mutation spectrum, we searched for mutations including exon deletions in six patients heterozygous for the GAA repeat expansion and found two unknown missense mutations, p.Asn146Lys and p.Leu186Arg, in trans to the expanded FRDA allele.
|
15340363 |
2004 |
rs138034837
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Here, we report three Turkish siblings from consanguineous parents presenting with a CMT-like phenotype who carry a homozygous c.493C>T, p.Arg165Cys mutation in the FXN gene that is the only known causative gene for Friedreich's ataxia (FRDA).
|
31673878 |
2020 |
rs138471431
|
|
|
0.710 |
GeneticVariation |
BEFREE |
The point mutations I154F and W155R in frataxin cause FRDA and are clustered to one surface of the protein, and these mutations decrease the interaction of frataxin with ISD11.
|
17331979 |
2007 |
rs143396368
|
|
|
0.010 |
GeneticVariation |
BEFREE |
p.R165P patients progress to a less disabling disease state than typical FRDA.
|
24816001 |
2014 |
rs148443992
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To reinvestigate the mutation spectrum, we searched for mutations including exon deletions in six patients heterozygous for the GAA repeat expansion and found two unknown missense mutations, p.Asn146Lys and p.Leu186Arg, in trans to the expanded FRDA allele.
|
15340363 |
2004 |
rs104894106
|
|
T |
0.810 |
CausalMutation |
CLINVAR |
|
|
|
rs104894105
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs104894107
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs146818694
|
|
G |
0.720 |
CausalMutation |
CLINVAR |
|
|
|
rs104894108
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs140987490
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs141935559
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs56214919
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs886037630
|
|
TACACCTTGAGGACA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A novel missense mutation (L198R) in the Friedreich's ataxia gene.
|
10874325 |
2000 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
|
9989622 |
1999 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
The first cellular models based on frataxin missense mutations that reproduce spontaneously the defects associated with Friedreich ataxia.
|
19629184 |
2009 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.
|
9150176 |
1997 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.
|
10732799 |
1998 |
rs104894106
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Identification of a missense mutation in a Friedreich's ataxia patient: implications for diagnosis and carrier studies.
|
9779809 |
1998 |
rs104894105
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Atypical Friedreich ataxia caused by compound heterozygosity for a novel missense mutation and the GAA triplet-repeat expansion.
|
9150176 |
1997 |
rs104894105
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene.
|
10732799 |
1998 |
rs104894105
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A novel missense mutation (L198R) in the Friedreich's ataxia gene.
|
10874325 |
2000 |