VEP and SnpEff are good if you want a command-line tool to integrate into your pipeline. If you want to further investigate the consequences of just a couple of variants, you can try for example PredictSNP2, Consurf, ProtScale and Protter.
I was thinking to translate DNA sequence (without deletion and with deletion) into protein sequence and compare them using the tools you mentioned. Does this make sense to you?
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<p>Hello</p> <p>Can the UCSC browser be used to predict the effect of novel SNPs on a transcript (e.g. synonymous and non synonymous)? I was wondering …
VEP and SnpEff are good if you want a command-line tool to integrate into your pipeline. If you want to further investigate the consequences of just a couple of variants, you can try for example PredictSNP2, Consurf, ProtScale and Protter.
Or VEP online
I was thinking to translate DNA sequence (without deletion and with deletion) into protein sequence and compare them using the tools you mentioned. Does this make sense to you?