rs878853650
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
CDKN2A (p16INK4A) somatic and germline mutations.
|
8723678 |
1996 |
rs878853650
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
|
17047042 |
2006 |
rs878853650
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
Familial melanoma, pancreatic cancer and germline CDKN2A mutations.
|
15146471 |
2004 |
rs878853650
|
|
Hereditary Melanoma
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
rs878853650
|
|
Hereditary Melanoma
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds.
|
8595405 |
1995 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Novel germline p16 mutation in familial malignant melanoma in southern Sweden.
|
8653684 |
1996 |
rs878853650
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
Mutations of the CDKN2/p16INK4 gene in Australian melanoma kindreds.
|
8595405 |
1995 |
rs878853650
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
Geographical variation in the penetrance of CDKN2A mutations for melanoma.
|
12072543 |
2002 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Germline mutations of the CDKN2 gene in UK melanoma families.
|
9328469 |
1997 |
rs878853650
|
|
Hereditary Melanoma
|
G |
0.700 |
CausalMutation
|
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families.
|
11506491 |
2001 |
rs878853650
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
The p16INK4a/CDKN2A tumor suppressor and its relatives.
|
9823374 |
1998 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Five novel somatic CDKN2/p16 mutations identified in melanoma, glioma and carcinoma of the pancreas. Mutations in brief no. 170. Online.
|
10651484 |
1998 |
rs878853650
|
|
Hereditary Melanoma
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
CDKN2A germline mutations in individuals with cutaneous malignant melanoma.
|
17218939 |
2007 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
CDKN2A mutations in Spanish cutaneous malignant melanoma families and patients with multiple melanomas and other neoplasia.
|
10874641 |
1999 |
rs878853650
|
|
Neoplastic Syndromes, Hereditary
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample.
|
16234564 |
2005 |
rs878853650
|
|
Hereditary Melanoma
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
Coexisting NRAS and BRAF mutations in primary familial melanomas with specific CDKN2A germline alterations.
|
19759551 |
2010 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population.
|
8710906 |
1996 |
rs878853650
|
|
Hereditary Melanoma
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
|
16905682 |
2007 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
A novel L94Q mutation in the CDKN2A gene in a melanoma kindred.
|
14646619 |
2003 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group.
|
9425228 |
1998 |
rs878853650
|
|
Hereditary Melanoma
|
G |
0.700 |
GeneticVariation
|
CLINVAR |
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
|
17047042 |
2006 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Germline p16 mutations in familial melanoma.
|
7987387 |
1994 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients.
|
19260062 |
2009 |
rs878853650
|
|
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 2
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Germline mutation of ARF in a melanoma kindred.
|
12019208 |
2002 |