Hi

Can you please tell me the exact and best or few Softwares/ Data bases, which will used to check the new variations  in a sample 

I am doing Sequencing of the Beta catenin gene in leukemia(AML), I got the sequencing results and got some variations  which are known in literature. Besides that I got more more variations in the sample when compared with the original reference sequence

I need help how can i confirm these additional changes , whether these are SNPs, new Novel variations etc, please suggest the softwares/ data bases where i can check and compare and report exactly the variations and SNPs  

Like there is WebHome < MITOMAP < MITOWEB , for mitochondrial sequence check

Please suggest similar software/databases for whole  human genome or for single genes ( like for B catenin gene)

Thanks in Advance 

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