Annovar Output column "AAChange.knowngene" has different values for codon and AA change. eg: Chr chr7 Start 50467736 End 50467736 Ref C Alt G Func.knowngene exonic Gene.knowngene IKZF1 GeneDetail.knowngene 0 ExonicFunc.knowngene nonsynonymous SNV AAChange.knowngene IKZF1:uc010kyx.3:exon2:c.C191G:p.A64G,IKZF1:uc022acs.1:exon3:c.C161G:p.A54G,IKZF1:uc003tpa.4:exon4:c.C266G:p.A89G,IKZF1:uc022acr.1:exon4:c.C296G:p.A99G,IKZF1:uc022acq.1:exon5:c.C542G:p.A181G,IKZF1:uc022acy.1:exon5:c.C392G:p.A131G,IKZF1:uc022acz.1:exon5:c.C422G:p.A141G,IKZF1:uc003toz.4:exon6:c.C881G:p.A294G,IKZF1:uc022acv.1:exon6:c.C554G:p.A185G,IKZF1:uc022acw.1:exon6:c.C584G:p.A195G,IKZF1:uc022acx.1:exon6:c.C710G:p.A237G,IKZF1:uc003tox.4:exon7:c.C845G:p.A282G,IKZF1:uc003toy.4:exon7:c.C845G:p.A282G,IKZF1:uc011kck.2:exon7:c.C710G:p.A237G,IKZF1:uc022act.1:exon7:c.C680G:p.A227G,IKZF1:uc022acu.1:exon7:c.C710G:p.A237G,IKZF1:uc003tow.4:exon8:c.C971G:p.A324G cosmic70 0 clinvar_20140929 0 dbnsfp30a 0.134 SIFT_score 0.16 SIFT_pred T Polyphen2_HDIV_score 1 Polyphen2_HDIV_pred D LRT_score 0 LRT_pred D FATHMM_score 4.31 FATHMM_pred T MutationTaster_score 1 MutationTaster_pred D
Which of the transcripts and/or protien/codon change annotated is important while considering the mutation?