Variant: rs104894359 

    present in Gene: KRAS
    present in Chromosome: 12
    Position on Chromosome: 25227346
    Alleles of this Variant: C/G;T

rs104894359 in KRAS gene and CARDIOFACIOCUTANEOUS SYNDROME 2 PMID 16474405 2006 Germline KRAS mutations cause Noonan syndrome.

PMID 17056636 2007 Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations.

PMID 16474404 2006 Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.

PMID 21797849 2012 Two novel germline KRAS mutations: expanding the molecular and clinical phenotype.

PMID 20949621 2011 Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders.

rs104894359 in KRAS gene and Cardio-facio-cutaneous syndrome PMID 17056636 2007 Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations.

PMID 20949621 2011 Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders.

PMID 16474404 2006 Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.

rs104894359 in KRAS gene and NOONAN SYNDROME 3 PMID 19396835 2009 Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutations.

PMID 16773572 2006 Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype.

PMID 20876176 2010 Noonan syndrome: clinical features, diagnosis, and management guidelines.

PMID 17056636 2007 Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations.

PMID 20949621 2011 Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders.

PMID 16474405 2006 Germline KRAS mutations cause Noonan syndrome.

PMID 17468812 2007 Further evidence of genetic heterogeneity in Costello syndrome: involvement of the KRAS gene.

rs104894359 in KRAS gene and Noonan Syndrome PMID 17056636 2007 Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations.

PMID 16474404 2006 Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.

PMID 20949621 2011 Germline KRAS mutations cause aberrant biochemical and physical properties leading to developmental disorders.