rs104894094
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
|
16905682 |
2007 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations of the CDKN2 gene in UK melanoma families.
|
9328469 |
1997 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.
|
9699728 |
1998 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKN2A mutation in a non-FAMMM kindred with cancers at multiple sites results in a functionally abnormal protein.
|
9389568 |
1997 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group.
|
9425228 |
1998 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
A novel methionine-53-valine mutation of p16 in a hereditary melanoma kindred.
|
15304098 |
2004 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
The M53I mutation in CDKN2A is a founder mutation that predominates in melanoma patients with Scottish ancestry.
|
17171691 |
2007 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds.
|
8595405 |
1995 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Functional impairment of melanoma-associated p16(INK4a) mutants in melanoma cells despite retention of cyclin-dependent kinase 4 binding.
|
11595726 |
2001 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKN2A mutations in Scottish families with cutaneous melanoma: results from 32 newly identified families.
|
16307646 |
2005 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population.
|
8710906 |
1996 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Biologic and biochemical analyses of p16(INK4a) mutations from primary tumors.
|
10491434 |
1999 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKN2A mutations in multiple primary melanomas.
|
9516223 |
1998 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds.
|
8570179 |
1995 |
rs104894095
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Genetic discrimination and health insurance: an urgent need for reform.
|
7569991 |
1995 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome.
|
11815963 |
2002 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutation testing in melanoma families: INK4A, CDK4 and INK4D.
|
10390011 |
1999 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKN2A germline mutations in U.K. patients with familial melanoma and multiple primary melanomas.
|
9699728 |
1998 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKN2A mutations in multiple primary melanomas.
|
9516223 |
1998 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Analysis of the p16 gene, CDKN2, in 17 Australian melanoma kindreds.
|
8570179 |
1995 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Functional impairment of melanoma-associated p16(INK4a) mutants in melanoma cells despite retention of cyclin-dependent kinase 4 binding.
|
11595726 |
2001 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Longitudinal assessment of the nevus phenotype in a melanoma kindred.
|
15304099 |
2004 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Classifying variants of CDKN2A using computational and laboratory studies.
|
21462282 |
2011 |