Mainly I am interested to know what are the tools /ways I can annotate a SNP in intron to see whether the SNP has some
functional implication on host gene function etc.. Please share your thoughts.
I have considered allowing the longer but incorrect forms to go through unfortunately that is a slippery slope because then it may allow other badly formed urls and only confuses the search engines that do not know anymore which one is the correct url
Lately I have been testing out Ingenuity Variant Analysis which seems to be doing a good job of prioritizing variants in non-coding regions if you choose the right filters. But, not sure if you (or we) can afford to use this system outside of a context of the free trial period or promotional pilot programs. I think their pricing model is still TBD.
I have considered allowing the longer but incorrect forms to go through unfortunately that is a slippery slope because then it may allow other badly formed urls and only confuses the search engines that do not know anymore which one is the correct url