Variant: rs121913668 

    present in Gene: MET
    present in Chromosome: 7
    Position on Chromosome: 116778827
    Alleles of this Variant: T/C

rs121913668 in MET gene and Neoplastic Syndromes, Hereditary PMID 10327054 1999 Novel mutations of the MET proto-oncogene in papillary renal carcinomas.

PMID 9326629 1997 Activating mutations for the met tyrosine kinase receptor in human cancer.

PMID 11354004 2001 Structural basis of oncogenic activation caused by point mutations in the kinase domain of the MET proto-oncogene: modeling studies.

PMID 9140397 1997 Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas.

rs121913668 in MET gene and Renal Cell Carcinoma PMID 9140397 1997 Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas.

rs121913668 in MET gene and Type 1 Papillary Renal Cell Carcinoma PMID 10417759 1999 Novel mutation in the ATP-binding site of the MET oncogene tyrosine kinase in a HPRCC family.

PMID 9140397 1997 Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas.

PMID 24319509 2013 Canadian guideline on genetic screening for hereditary renal cell cancers.

PMID 25394175 2015 A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment.

PMID 10433944 1999 Hereditary and sporadic papillary renal carcinomas with c-met mutations share a distinct morphological phenotype.

PMID 9563489 1998 Two North American families with hereditary papillary renal carcinoma and identical novel mutations in the MET proto-oncogene.

PMID 10327054 1999 Novel mutations of the MET proto-oncogene in papillary renal carcinomas.