×
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
×
Entrez Id:
1029
Gene Symbol:
CDKN2A
CDKN2A
0.110
CausalMutation
group
CLINVAR
Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden).
10956390
2000