rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Novel germline p16 mutation in familial malignant melanoma in southern Sweden.
|
8653684 |
1996 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Functional evaluation of tumour-specific variants of p16INK4a/CDKN2A: correlation with protein structure information.
|
10498896 |
1999 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families.
|
10922411 |
2000 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
CDKN2A germ-line mutations in individuals with multiple cutaneous melanomas.
|
11156381 |
2000 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families.
|
11319798 |
2001 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Geographical variation in the penetrance of CDKN2A mutations for melanoma.
|
12072543 |
2002 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Familial melanoma, pancreatic cancer and germline CDKN2A mutations.
|
15146471 |
2004 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
|
16905682 |
2007 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
|
17047042 |
2006 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Swedish CDKN2A mutation carriers do not present the atypical mole syndrome phenotype.
|
20526219 |
2010 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
High risk of tobacco-related cancers in CDKN2A mutation-positive melanoma families.
|
24935963 |
2014 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Molecular characterization of melanoma cases in Denmark suspected of genetic predisposition.
|
25803691 |
2015 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Germline mutations predisposing to non-small cell lung cancer.
|
25813228 |
2015 |
rs768966657
|
|
Neoplastic Syndromes, Hereditary
|
AGAC |
0.700 |
CausalMutation
|
CLINVAR |
Germline CDKN2A Mutation Status and Survival in Familial Melanoma Cases.
|
27287845 |
2016 |