Variant: rs121913386 

    present in Gene: CDKN2A
    present in Chromosome: 9
    Position on Chromosome: 21971018
    Alleles of this Variant: G/A;T

rs121913386 in CDKN2A gene and Cutaneous Melanoma PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

rs121913386 in CDKN2A gene and Neoplastic Syndromes, Hereditary PMID 8755727 1996 Tumor suppressor p16INK4A: structural characterization of wild-type and mutant proteins by NMR and circular dichroism.

PMID 9856841 1998 CDKN2a/p16INK4a mutations and lack of p19ARF involvement in familial melanoma kindreds.

PMID 21462282 2011 Classifying variants of CDKN2A using computational and laboratory studies.

PMID 17992122 2007 The p.G23S CDKN2A founder mutation in high-risk melanoma families from Central Italy.

PMID 8668202 1996 Temperature-sensitive mutants of p16CDKN2 associated with familial melanoma.

PMID 15140233 2004 p16INK4a and p14ARF tumor suppressor genes are commonly inactivated in cutaneous squamous cell carcinoma.

PMID 15146471 2004 Familial melanoma, pancreatic cancer and germline CDKN2A mutations.

rs121913386 in CDKN2A gene and Squamous cell carcinoma of lung PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

rs121913386 in CDKN2A gene and Squamous cell carcinoma of skin PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

rs121913386 in CDKN2A gene and Squamous cell carcinoma of the head and neck PMID 26619011 2016 Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity.

rs121913386 in CDKN2A gene and melanoma PMID 25157968 2014 Prospective enterprise-level molecular genotyping of a cohort of cancer patients.