rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
|
27854360 |
2017 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.
|
25394175 |
2015 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing.
|
25356965 |
2015 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
|
24893135 |
2014 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Canadian guideline on genetic screening for hereditary renal cell cancers.
|
24319509 |
2013 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
|
23788249 |
2013 |
rs869025631
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Structural bioinformatics mutation analysis reveals genotype-phenotype correlations in von Hippel-Lindau disease and suggests molecular mechanisms of tumorigenesis.
|
19408298 |
2009 |
rs869025631
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Germline mutations in the von Hippel-Lindau disease (VHL) gene in mainland Chinese families.
|
18446368 |
2008 |
rs869025631
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Genotype-phenotype correlations in von Hippel-Lindau disease.
|
17024664 |
2007 |
rs869025631
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Trichloroethylene exposure and somatic mutations of the VHL gene in patients with Renal Cell Carcinoma.
|
17997830 |
2007 |
rs869025631
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
[Germ line mutations in Chinese kindreds with von Hippel-Lindau syndrome].
|
17407064 |
2007 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
The von Hippel-Lindau (VHL) germline mutation V84L manifests as early-onset bilateral pheochromocytoma.
|
16502427 |
2006 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors.
|
15604628 |
2004 |
rs869025631
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Genetic characterization and structural analysis of VHL Spanish families to define genotype-phenotype correlations.
|
14722919 |
2004 |
rs869025631
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Comparative sequence analysis (CSA): a new sequence-based method for the identification and characterization of mutations in DNA.
|
11058902 |
2000 |
rs869025631
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation.
|
10088816 |
1999 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Formation of the VHL-elongin BC tumor suppressor complex is mediated by the chaperonin TRiC.
|
10635329 |
1999 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene.
|
10533030 |
1999 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations of the VHL gene in sporadic renal cell carcinoma: definition of a risk factor for VHL patients to develop an RCC.
|
10408776 |
1999 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Variable penetrance of familial pheochromocytoma associated with the von Hipple Lindau gene mutation, S68W. Mutations in brief no. 150. Online.
|
10627136 |
1998 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene.
|
9829911 |
1998 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germline mutations detected in the von Hippel-Lindau disease tumor suppressor gene by Southern blot and direct genomic DNA sequencing.
|
9452032 |
1998 |
rs869025631
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene.
|
9829911 |
1998 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Three novel mutations in the Von Hippel-Lindau tumour suppressor gene in Italian patients.
|
9452106 |
1998 |
rs869025631
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma.
|
9829912 |
1998 |