I have sequenced an intronic fragment. I want to find mutations or polymorphisms in the fragment.
Please go to http://molbiol-tools.ca/,
then to DNA Sequence Analysis,
then check "Translation"
I agree with views of Dr Pritam.
Thanks, Prof Meyer and Dr. Panda.
Whatsoever, I'm still struggling to correlate my intronic variants with the disease I'm working on. Yes, my intronic sequence have some splicing site, donor sites - but I can not find a way to correlate these with any of the disease features.
Would you like to share those variants? what kind of variants are they even if they are a part of ESE/ ISS sites.
Now, I can corelate it with disease. It has ESE site. Thank you Prof Atif Baig.
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