Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population.
|
8710906 |
1996 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
Functional reassessment of P16 variants using a transfection-based assay.
|
10389768 |
1999 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
Estimating the relative risk of developing melanoma in INK4A carriers.
|
15075790 |
2004 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Genotype-phenotype relationships in U.S. melanoma-prone families with CDKN2A and CDK4 mutations.
|
10861313 |
2000 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Indication for CDKN2A-mutation analysis in familial pancreatic cancer families without melanomas.
|
22636603 |
2012 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Functional analysis of CDKN2A/p16INK4a 5'-UTR variants predisposing to melanoma.
|
20093296 |
2010 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
Biologic and biochemical analyses of p16(INK4a) mutations from primary tumors.
|
10491434 |
1999 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Multiple primary melanomas in a CDKN2A mutation carrier exposed to ionizing radiation.
|
18025365 |
2007 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study.
|
20876876 |
2010 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Mutation screening of the CDKN2A promoter in melanoma families.
|
10738302 |
2000 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
Novel CDKN2A mutations detected in western Swedish families with hereditary malignant melanoma.
|
17255954 |
2007 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
The missing puzzle piece: splicing mutations.
|
24294354 |
2013 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families.
|
12700603 |
2003 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Germline CDKN2A Mutation Status and Survival in Familial Melanoma Cases.
|
27287845 |
2016 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
Familial melanoma: clinical factors associated with germline CDKN2A mutations according to the number of patients affected by melanoma in a family.
|
22841127 |
2012 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Familial melanoma-associated mutations in p16 uncouple its tumor-suppressor functions.
|
23190892 |
2013 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.
|
9699728 |
1998 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer.
|
21614589 |
2011 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition.
|
25803691 |
2015 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds.
|
8595405 |
1995 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
GeneticVariation
|
group |
CLINVAR |
Analysis of p16INK4a and its interaction with CDK4.
|
8573142 |
1996 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.
|
7640518 |
1995 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Prospective risk of cancer and the influence of tobacco use in carriers of the p16-Leiden germline variant.
|
25227142 |
2015 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
0.110 |
CausalMutation
|
group |
CLINVAR |
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group.
|
9425228 |
1998 |