Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.645278;Hs.645279 8q24.3 610596

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer C A Missense p.D65Y c.193G>T 8 145512892 LUSC C T Missense p.D78N c.232G>A 8 145512853 BLCA G C Missense p.S53C c.158C>G 8 145512927 BLCA