Hi To analysis exome sequence data sometimes people exclude synonymous mutation.BUT it might affect on splice sites depend on how far it is from splice sites.
I have a list of synonymous variants.What is the easiest way to analyze these kind of mutations.I mean an on line web page where I upload my variants list and have a batch output.Thanks
Hi. How did you call these synonymous variants? If you used PolyPhen etc., I think it would have told you if the mutation is splice site mutation.