Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
Biomarker |
CTD_human |
|
|
|
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
Biomarker |
CLINGEN |
A p16INK4a-insensitive CDK4 mutant targeted by cytolytic T lymphocytes in a human melanoma.
|
7652577 |
1995 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
CausalMutation |
CLINVAR |
A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-prone families.
|
10869234 |
2000 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
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
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
CausalMutation |
CLINVAR |
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus.
|
7987388 |
1994 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
CausalMutation |
CLINVAR |
BRCA1, BRCA2, PALB2, and CDKN2A mutations in familial pancreatic cancer: a PACGENE study.
|
25356972 |
2015 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
Biomarker |
CLINGEN |
Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene.
|
7666917 |
1995 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
CDKN2A and CDK4 mutation analysis in Italian melanoma-prone families: functional characterization of a novel CDKN2A germ line mutation.
|
11556834 |
2001 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
CDKN2A germline mutations in individuals with cutaneous malignant melanoma.
|
17218939 |
2007 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.
|
9699728 |
1998 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
CausalMutation |
CLINVAR |
CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma.
|
18983535 |
2008 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
CDKN2A mutations in multiple primary melanomas.
|
9516223 |
1998 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
CDKN2A point mutations D153spl(c.457G>T) and IVS2+1G>T result in aberrant splice products affecting both p16INK4a and p14ARF.
|
12853981 |
2003 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
CausalMutation |
CLINVAR |
Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma.
|
26681309 |
2016 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
Characterization of individuals at high risk of developing melanoma in Latin America: bases for genetic counseling in melanoma.
|
26681309 |
2016 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
CausalMutation |
CLINVAR |
Classifying variants of CDKN2A using computational and laboratory studies.
|
21462282 |
2011 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
Classifying variants of CDKN2A using computational and laboratory studies.
|
21462282 |
2011 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
Clinical features predicting identification of CDKN2A mutations in Italian patients with familial cutaneous melanoma.
|
21893440 |
2011 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
Comprehensive mutational analysis of CDKN2A and CDK4 in Greek patients with cutaneous melanoma.
|
21801156 |
2011 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
Familial melanoma, pancreatic cancer and germline CDKN2A mutations.
|
15146471 |
2004 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
CausalMutation |
CLINVAR |
Familial melanoma-associated mutations in p16 uncouple its tumor-suppressor functions.
|
23190892 |
2013 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
CLINVAR |
Familial melanoma-associated mutations in p16 uncouple its tumor-suppressor functions.
|
23190892 |
2013 |
Entrez Id: |
1029 |
Gene Symbol: |
CDKN2A |
CDKN2A
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
GeneticVariation |
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
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
CausalMutation |
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
|
MELANOMA-PANCREATIC CANCER SYNDROME
|
0.600 |
CausalMutation |
CLINVAR |
Functional analysis of CDKN2A/p16INK4a 5'-UTR variants predisposing to melanoma.
|
20093296 |
2010 |