rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Mutation testing in melanoma families: INK4A, CDK4 and INK4D.
|
10390011 |
1999 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
A CDKN2A mutation in familial melanoma that abrogates binding of p16INK4a to CDK4 but not CDK6.
|
17909018 |
2007 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Role of key-regulator genes in melanoma susceptibility and pathogenesis among patients from South Italy.
|
19799798 |
2009 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKN2A (P16(INK4a)) and CDK4 mutation analysis in 131 Australian melanoma probands: effect of family history and multiple primary melanomas.
|
10398427 |
1999 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
CDKN2A mutations in multiple primary melanomas.
|
9516223 |
1998 |
rs104894097
|
|
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 |
rs104894097
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Comprehensive mutational analysis of CDKN2A and CDK4 in Greek patients with cutaneous melanoma.
|
21801156 |
2011 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
rs104894097
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Lifetime risk of melanoma in CDKN2A mutation carriers in a population-based sample.
|
16234564 |
2005 |
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 |
Familial melanoma, pancreatic cancer and germline CDKN2A mutations.
|
15146471 |
2004 |
rs104894098
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Familial melanoma-associated mutations in p16 uncouple its tumor-suppressor functions.
|
23190892 |
2013 |
rs104894098
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Classifying variants of CDKN2A using computational and laboratory studies.
|
21462282 |
2011 |
rs104894098
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
A common founder for the V126D CDKN2A mutation in seven North American melanoma-prone families.
|
11506491 |
2001 |
rs104894098
|
|
T |
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 |
rs104894098
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Temperature-sensitive mutants of p16CDKN2 associated with familial melanoma.
|
8668202 |
1996 |
rs104894098
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional reassessment of P16 variants using a transfection-based assay.
|
10389768 |
1999 |
rs104894098
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutations associated with familial melanoma impair p16INK4 function.
|
7647780 |
1995 |
rs104894098
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline p16 mutations in familial melanoma.
|
7987387 |
1994 |
rs104894098
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Predicting functional significance of cancer-associated p16(INK4a) mutations in CDKN2A.
|
20340136 |
2010 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
The p16INK4a/CDKN2A tumor suppressor and its relatives.
|
9823374 |
1998 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Role of the CDKN2A locus in patients with multiple primary melanomas.
|
15860862 |
2005 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Clinical features predicting identification of CDKN2A mutations in Italian patients with familial cutaneous melanoma.
|
21893440 |
2011 |
rs104894099
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
|
16905682 |
2007 |