Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34589476
rs34589476
MET
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.730 GeneticVariation BEFREE Subsequent sequence analysis revealed a heterozygous R988C mutation of the MET gene and a VHL deletion in both the primary tumor and the tumor-derived ccRCC cell line. 24929890

2014
dbSNP: rs34589476
rs34589476
MET
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.730 GeneticVariation BEFREE A new missense c-Met mutation N948S was identified in cell lines and R988C in tumor tissue in the juxtamembrane domain of c-Met. 17404109

2007
dbSNP: rs34589476
rs34589476
MET
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.730 GeneticVariation BEFREE These include two different c-MET missense mutations in the juxtamembrane (JM) domain (R988C found in NCI-H69 and H249 cell lines; and T1010I in SCLC tumor sample T31). 14559814

2003