|
rs1055680335
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1560241522
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs144023803
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosa.
|
7833933 |
1994 |
|
rs757415879
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Aminoglycosides restore full-length type VII collagen by overcoming premature termination codons: therapeutic implications for dystrophic epidermolysis bullosa.
|
25155989 |
2014 |
|
rs121912856
|
|
C |
0.720 |
CausalMutation |
CLINVAR |
Analysis of the COL7A1 gene in Czech patients with dystrophic epidermolysis bullosa reveals novel and recurrent mutations.
|
20598510 |
2010 |
|
rs757415879
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Cetuximab therapy of metastasizing cutaneous squamous cell carcinoma in a patient with severe recessive dystrophic epidermolysis bullosa.
|
19439919 |
2009 |
|
rs144023803
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation.
|
9326325 |
1997 |
|
rs757415879
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
COL7A1 mutational analysis in Korean patients with dystrophic epidermolysis bullosa.
|
17916216 |
2007 |
|
rs1032335328
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Comparative mutation detection screening of the type VII collagen gene (COL7A1) using the protein truncation test, fluorescent chemical cleavage of mismatch, and conformation sensitive gel electrophoresis.
|
10504458 |
1999 |
|
rs144023803
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Comparative mutation detection screening of the type VII collagen gene (COL7A1) using the protein truncation test, fluorescent chemical cleavage of mismatch, and conformation sensitive gel electrophoresis.
|
10504458 |
1999 |
|
rs757415879
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Comparative mutation detection screening of the type VII collagen gene (COL7A1) using the protein truncation test, fluorescent chemical cleavage of mismatch, and conformation sensitive gel electrophoresis.
|
10504458 |
1999 |
|
rs886058642
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Comparative mutation detection screening of the type VII collagen gene (COL7A1) using the protein truncation test, fluorescent chemical cleavage of mismatch, and conformation sensitive gel electrophoresis.
|
10504458 |
1999 |
|
rs757415879
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Dystrophic epidermolysis bullosa complicated by cutaneous squamous cell carcinoma and pulmonary and renal amyloidosis.
|
12653705 |
2003 |
|
rs1057517723
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages.
|
27899325 |
2017 |
|
rs747912732
|
|
TC |
0.700 |
GeneticVariation |
CLINVAR |
Epidermolysis bullosa. II. Type VII collagen mutations and phenotype-genotype correlations in the dystrophic subtypes.
|
16971478 |
2007 |
|
rs886058642
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Epidermolysis bullosa. II. Type VII collagen mutations and phenotype-genotype correlations in the dystrophic subtypes.
|
16971478 |
2007 |
|
rs757415879
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Expanding the COL7A1 mutation database: novel and recurrent mutations and unusual genotype-phenotype constellations in 41 patients with dystrophic epidermolysis bullosa.
|
16484981 |
2006 |
|
rs144023803
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial.
|
24032424 |
2013 |
|
rs1057517723
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohort.
|
19681861 |
2009 |
|
rs757415879
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Genotype-phenotype correlation in recessive dystrophic epidermolysis bullosa: when missense doesn't make sense.
|
15816848 |
2005 |
|
rs121912836
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Given the widespread geographical distribution of this mutation and the demonstration of its occurrence as a de novo event, G2043R therefore represents the first example of a mutational hotspot in dominant DEB.
|
9892921 |
1998 |
|
rs144023803
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Haplotype analysis revealed that the mutations existed on similar allelic backgrounds in different patients, consistent with propagation of common British ancestral haplotypes, although R578X and 7786delG also have been described in DEB patients from other ethnic backgrounds.
|
9242516 |
1997 |
|
rs144023803
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
HB-EGF induces COL7A1 expression in keratinocytes and fibroblasts: possible mechanism underlying allogeneic fibroblast therapy in recessive dystrophic epidermolysis Bullosa.
|
21471992 |
2011 |
|
rs757415879
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
High frequency of the 425A-->G splice-site mutation and novel mutations of the COL7A1 gene in central Europe: significance for future mutation detection strategies in dystrophic epidermolysis bullosa.
|
15888141 |
2005 |
|
rs121912856
|
|
C |
0.720 |
CausalMutation |
CLINVAR |
High frequency of the 425A-->G splice-site mutation and novel mutations of the COL7A1 gene in central Europe: significance for future mutation detection strategies in dystrophic epidermolysis bullosa.
|
15888141 |
2005 |