Entering edit mode
3.6 years ago
Maguelonne
•
0
Hello,
I have questions regarding the RefSeq annotation of ANNOVAR.
When a variant is "exonic" (Func_refGene=exonic) and several transcripts are described in the "AAChange_refGene" annotation, is the ExonicFunc_refGene annotation valid for all the transcripts listed in the "AAChange_refGene" annotation of this variant?
If so, how is it possible to identify the canonical transcript? It not, which one of the transcripts listed in "AAChange_refGene" corresponds to the predicted ExonicFunc_refGene?
Thank you in advance for your help!
